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| Product | Description | |
|---|---|---|
| PEG 400 | PEG 400 (polyethylene glycol 400) is a low-molecular-weight grade of polyethylene glycol. It is a clear, colorless, viscous liquid. Due in part to its low toxicity, PEG 400 is widely used in a variety of pharmaceutical formulations. CAS No. 25322-68-3. Product ID: PE-0072. Molecular formula: C2H6O2. Mole weight: 62.0678. Category: Suspending Agents. Product Keywords: Pharmaceutical Excipients; Liquid Dosage Form; Suspending Agents; PEG 400; PE-0072; C2H6O2; 25322-68-3; 25322-68-3. Appearance: Clear colorless viscous liquid. EC Number: 500-038-2. Synonym(s): polyethylene glycol. Storage: 2-8ºC. Boiling Point: 250ºC. Melting Point: -65ºC. Density: 1.125 g/cm3. |  |
| PEG 400 | PEG 400 (polyethylene glycol 400) is a low-molecular-weight grade of polyethylene glycol. It is a clear, colorless, viscous liquid. Due in part to its low toxicity, PEG 400 is widely used in a variety of pharmaceutical formulations. CAS No. 25322-68-3. Product ID: PE-0075. Molecular formula: C2H6O2. Mole weight: 62.0678. Category: Wetting Agents. Product Keywords: Pharmaceutical Excipients; Liquid Dosage Form; Solid Dosage Form; Wetting Agents; PEG 400; PE-0075; C2H6O2; 25322-68-3; 25322-68-3. Appearance: Clear colorless viscous liquid. EC Number: 500-038-2. Synonym(s): polyethylene glycol. Storage: 2-8ºC. Boiling Point: 250ºC. Melting Point: -65ºC. Density: 1.125 g/cm3. | |
| PEG 400 | PEG 400 (polyethylene glycol 400) is a low-molecular-weight grade of polyethylene glycol. It is a clear, colorless, viscous liquid. Due in part to its low toxicity, PEG 400 is widely used in a variety of pharmaceutical formulations. CAS No. 25322-68-3. Product ID: PE-0171. Molecular formula: C2H6O2. Mole weight: 62.0678. Category: Filler. Product Keywords: Pharmaceutical Excipients; Solid Dosage Form; Capsule Excipients; Filler; PEG 400; PE-0171; C2H6O2; 25322-68-3; 25322-68-3. Appearance: Clear colorless viscous liquid. EC Number: 500-038-2. Synonym(s): polyethylene glycol. Storage: 2-8ºC. Boiling Point: 250ºC. Melting Point: -65ºC. Density: 1.125 g/cm3. | |
| PEG400 | PEG400 is a strongly hydrophilic polyethylene glycol used as an excellent solvent for a large number of substances. PEG400 is widely used in a variety of pharmaceutical formulations. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: Polyethylene glycol 400. CAS No. 25322-68-3. Pack Sizes: 50 mL; 100 mL. Product ID: HY-Y0873A. |  |
| PEG Solution (50% PEG 4000) | PEG Solution (50% PEG 4000). Group: Molecular Biology. Pack Sizes: 300ul. US Biological Life Sciences. |  Worldwide |
| Polyethylene Glycol 400 (PEG 400) | Poly(ethylene Glycol) ~400 is a polymer of ethylene oxide with a molecular weight of ~400 Daltons. Poly(ethylene Glycol) ~400 is considered a low molecular weight polyethylene glycol, and is used as a hydrophilic molecular probe for measuring intestinal permeability. Poly(ethylene Glycol) ~400 is also used as a hydrophilic plasticizer. Group: Biochemicals. Alternative Names: Polyglycol; Polyethylene oxide; Polyoxyethylene. Grades: Highly Purified. CAS No. 25322-68-3. Pack Sizes: 1L, 5L. Molecular Formula: (C?H?O)nH?O, Molecular Weight: ~400. US Biological Life Sciences. | Worldwide |
| Propylene Glycol 400 (PEG-400) | Propylene Glycol 400 (PEG-400). |  CA, FL & NJ |
| rac Ketoprofen PEG 400 Ester | rac Ketoprofen PEG 400 Ester. Uses: For analytical and research use. Group: Impurity standards. Catalog: APS002875. Format: Neat. |  |
| 4arm-PEG40K-COOH | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: 4arm-PEG-COOH, 4arm-PEG-Carboxyl. Molecular formula: average Mn 40000. |  |
| 4arm-PEG40K-Maleimide | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: 4arm-PEG-MAL, 4arm-PEG-Maleimide. Molecular formula: average Mn 40000. | |
| 4arm-PEG40K-NH2 | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: 4arm-PEG-NH2, 4arm-PEG-amine. Molecular formula: average Mn 40000. | |
| 4arm-PEG40K-Succinimidyl Carboxymethyl Ester | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: 4arm-PEG-Succinimidyl Carboxymethyl Ester. Molecular formula: average Mn 40000. | |
| 4arm-PEG40K-Succinimidyl Glutarate | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: 4arm-PEG-Succinimidyl Glutarate. Molecular formula: average Mn 40000. | |
| 4arm-PEG40K-Succinimidyl Succinate | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: 4arm-PEG-Succinimidyl Succinate. Molecular formula: average Mn 40000. | |
| 8arm-PEG40K-COOH | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: 8arm-PEG-COOH. Molecular formula: average Mn 40000. | |
| 8arm-PEG40K-Maleimide | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: 8arm-PEG-Maleimide. Molecular formula: average Mn 40000. | |
| 8arm-PEG40K-NH2 | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: 8arm-PEG-NH2. Molecular formula: average Mn 40000. | |
| 8arm-PEG40K-Succinimidyl Glutarate | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Molecular formula: average Mn 40000. | |
| 8arm-PEG40K-Succinimidyl Succinate | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Molecular formula: average Mn 40000. | |
| (+)-Biotin-PEG2-azide | (+)-Biotin-PEG2-azide. Group: Polymers. CAS No. 945633-30-7. Product ID: 5-[(3aS,4S,6aR)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl]-N-[2-[2-(2-azidoethoxy)ethoxy]ethyl]pentanamide. Molecular formula: 400.5g/mol. Mole weight: C16H28N6O4S. C1C2C (C (S1)CCCCC (=O)NCCOCCOCCN=[N+]=[N-])NC (=O)N2. InChI=1S / C16H28N6O4S / c17-22-19-6-8-26-10-9-25-7-5-18-14 (23) 4-2-1-3-13-15-12 (11-27-13) 20-16 (24) 21-15 / h12-13, 15H, 1-11H2, (H, 18, 23) (H2, 20, 21, 24) / t12-, 13-, 15- / m0 / s1. OVEZMVONEJMGLZ-YDHLFZDLSA-N. | |
| Biotin-PEG2-Azide | Useful for biotinylation of reagents. Group: Biotin-peg. Alternative Names: Biotin-PEG2-Azide, Biotin PEG2 Azide. CAS No. 945633-30-7. Molecular formula: C16H28N6O4S. Mole weight: 400.5 g/mol. Appearance: Solid powder. Purity: ≥98%. IUPACName: N-(2-(2-(2-azidoethoxy)ethoxy)ethyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamide. Canonical SMILES: O=C1N[C@@]2 ([H])[C@@] (CS[C@H]2CCCCC (NCCOCCOCCN=[N+]=[N-])=O) ([H])N1. Catalog: BR00028303. |  |
| Biotin-PEG-Biotin | Useful for biotinylation of reagents. Group: Biotin-peg. Alternative Names: Biotin-PEG-Biotin; SCHEMBL15216220; Biotin-PEG-Biotin, MW 1,000; Biotin-PEG-Biotin, MW 2,000; Biotin-PEG-Biotin, MW 3,400. CAS No. 194920-55-3. Molecular formula: C26H44N6O6S2. Mole weight: 600.79 g/mol. Appearance: To be determined. Purity: ≥98%. IUPACName: N,N-((ethane-1,2-diylbis(oxy))bis(ethane-2,1-diyl))bis(5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamide). Canonical SMILES: O=C (CCCC[C@@H]1SC[C@] ([H]) (N2)[C@@]1 (NC2=O)[H])NCCOCCOCCNC (CCCC[C@@H]3SC[C@] ([H]) (N4)[C@@]3 (NC4=O)[H])=O. Catalog: BR00028301. | |
| Bis-PEG2-NHS Ester | Bis-PEG2-NHS Ester. Group: Biochemicals. Grades: Highly Purified. CAS No. 65869-63-8. Pack Sizes: 10mg, 25mg. Molecular Formula: C16H20N2O10, Molecular Weight: 400.34. US Biological Life Sciences. | Worldwide |
| Cholesterol Esterase, PEG Modified | PEG (Polyethylene glycol) modified cholesterol esterase (PEG Cholesterol Esterase) isone of our premier cholesterol esterase conjugates. Cholesterol esterase is an enzyme that catalyzes the hydrolysis of cholesterol esters into their sterol components and fatty acids. Cholesterol esterase has clinical applications in the determination of serum cholesterol combined with other enzymes. PEG modified cholesterol esterase shows better stability with good reactivity. All our labeled cholesterol esterase products were performed under mild reaction conditions to retain their maximum bioactivity. These conjugates were further purified by chromatography to ensure adequate applications both in-vitro and in-vivo. Conjugate ration: 20~50 peg5000/monomer. solubility: soluble in aqueous buffer. Group: Enzymes. Synonyms: PEG Cholesterol Esterase; Cholesterol Esterase-polyethylene glycol; CE-polyethylene glycol; CE-PEG; PEG-CE; PEG-Cholesterol Esterase. Cholesterol Esterase. Mole weight: ~65 kD for monomer; 400 kD for hexamer. Activity: >300 units/g. Storage: Store at -20°C. Form: Lyophilized powder. Source: Porcine pancreas. Species: Porcine. PEG Cholesterol Esterase; Cholesterol Esterase-polyethylene glycol; CE-polyethylene glycol; CE-PEG; PEG-CE; PEG-Cholesterol Esterase; Cholesterol Esterase, PEG Modified. Cat No: NATE-1587. |  |
| Ethylene Glycol | Ethylene glycol is a clear, colorless syrupy liquid. The primary hazard is the threat to the environment. Immediate steps should be taken to limit its spread to the environment. Since it is a liquid it can easily penetrate the soil and contaminate groundwater and nearby streams.;Liquid; WetSolid;PEG 400 is a clear, viscous, colourless or almost colourless hygroscopic liquid; PEG 3000, PEG 3350, PEG 4000, PEG 6000 and PEG 8000 are white or almost white solids with a waxy or paraffin-like appearance;Liquid;ODOURLESS COLOURLESS VISCOUS HYGROSCOPIC LIQUID.;COLOURLESS VISCOUS SLIGHTLY HYGROSCOPIC LIQUID.;Clear, colorless, syrupy, odorless liquid.;Clear, colorless, syrupy, odorless liquid. [antifreeze] [Note: A solid below 9°F.];Clear, colorless, syrupy (viscous) liquid at room temperature. Often colored fluorescent yellow-green when used in automotive antifreeze. Group: Polymers. Product ID: ethane-1,2-diol. Molecular formula: 62.07g/mol. Mole weight: (C2H4O)nH2O (n = number of ethylene oxide units corresponding to a molecular weight of 6 000, about 140); HOCH2CH2OH; HO(C2H4O)nH; CH2OHCH2OH; C2H6O2. C(CO)O. InChI=1S/C2H6O2/c3-1-2-4/h3-4H,1-2H2. LYCAIKOWRPUZTN-UHFFFAOYSA-N. | |
| LAP | LAP is a cytocompatible, water soluble, Type I photoinitiator. It is used in the polymerization of hydrogels or other polymeric materials, specifically in the photopolymerization of PEG-diacrylate. It is preferred over irgacure 2959 for biological applications because of its increased polymerization rates with 365 nm light and absorbance at 400 nm, which allows for polymerization with visible light. It enables cell encapsualation at reduced initiator concentration and longer wavelength light, which has been proved to reduce initiator toxicity and increase cell viability. Synonyms: P-Phenyl-P-(2,4,6-trimethylbenzoyl)phosphinic Acid; Phenyl(2,4,6-trimethylbenzoyl)-phosphinic Acid Lithium Salt; Lithium Phenyl-2,4,6-trimethylbenzoylphosphinate; Lithium PTMB phosphinate. Grades: ≥98% by HPLC. CAS No. 85073-19-4. Molecular formula: C16H16LiO3P. Mole weight: 294.21. |  |
| Monoethylene Glycol | Ethylene glycol is a clear, colorless syrupy liquid. The primary hazard is the threat to the environment. Immediate steps should be taken to limit its spread to the environment. Since it is a liquid it can easily penetrate the soil and contaminate groundwater and nearby streams.;Liquid; WetSolid;PEG 400 is a clear, viscous, colourless or almost colourless hygroscopic liquid; PEG 3000, PEG 3350, PEG 4000, PEG 6000 and PEG 8000 are white or almost white solids with a waxy or paraffin-like appearance;Liquid;ODOURLESS COLOURLESS VISCOUS HYGROSCOPIC LIQUID.;COLOURLESS VISCOUS SLIGHTLY HYGROSCOPIC LIQUID.;Clear, colorless, syrupy, odorless liquid.;Clear, colorless, syrupy, odorless liquid. [antifreeze] [Note: A solid below 9°F.];Clear, colorless, syrupy (viscous) liquid at room temperature. Often colored fluorescent yellow-green when used in automotive antifreeze. Group: Chemical resins. Product ID: ethane-1,2-diol. Molecular formula: 62.07g/mol. Mole weight: (C2H4O)nH2O (n = number of ethylene oxide units corresponding to a molecular weight of 6 000, about 140); HOCH2CH2OH; HO(C2H4O)nH; CH2OHCH2OH; C2H6O2. C(CO)O. InChI=1S/C2H6O2/c3-1-2-4/h3-4H,1-2H2. LYCAIKOWRPUZTN-UHFFFAOYSA-N. | |
| mPEG40K-MAL | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: mPEG-MAL, Methoxy-PEG-Maleimide. Molecular formula: average Mn 40000. | |
| mPEG40K-Succinimidyl Carboxymethyl Ester | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: mPEG-Succinimidyl Carboxymethyl Ester. Molecular formula: average Mn 40000. | |
| Octadecanoic acid,2-(2-hydroxyethoxy)ethyl ester | Heterocyclic Organic Compound. Alternative Names: PEG 600 MONOSTEARATE;PEG 6000 MONOSTEARATE;PEG 400 MONOSTEARATE;PEG 4000 MONOSTEARATE;PEG 1540 MONOSTEARATE;PEG 300 MONOSTEARATE;PEG 1000 MONOSTEARATE;POLYOXYL 400 MONOSTEARATE. CAS No. 106-11-6. Molecular formula: C22H44O4. Mole weight: 372.66. Appearance: Beads. Density: 0.933g/cm³. Catalog: ACM106116. | |
| Poly(D,L-lactide-co-glycolide)-block-poly(ethylene glycol)-block-poly(D,L-lactide-co-glycolide) based poly(ether ester urethane) | The polymers are bioresorbable aliphatic polyesters comprised of a range of different ratios of lactide and glycolide monomers, PLA stereochemistries, and end-group functionalization. These biodegradeable homopolymers and copolymers of lactide and glycolide afford a variety of properties that range from very stiff, hard semi-crystalline materials with long degradation times, to softer, amorphous materials with faster degradation rates. Uses: This poly(ether ester urethane) based on plga-peg-plga triblock copolymers linked with a diisocyanate is a biodegradable, resorbable gel former for use in drug delivery systems. Group: Biodegradable polymers. Alternative Names: poly(ester ether urethane), PLGA-PEG-PLGA urethane, PEEU. Pack Sizes: 1, 5 g in glass bottle. Molecular formula: PEG average Mn 400 average Mn (6,000-15,000). Mole weight: [C2H2N2O2R[ (C3H4O2)x (C2H2O2)y]m[C2H4O]lO[ (C3H4O2)x (C2H2O2)y]m]n. CC (N[R]NC (OC (C)C (OCC (OCCOC (C (C)OC (COC)=O)=O)=O)=O)=O)=O. CC (N[R]NC (OCCCOC)=O)=O. | |
| Polyethylene Glycol 1000 | Ethylene glycol is a clear, colorless syrupy liquid. The primary hazard is the threat to the environment. Immediate steps should be taken to limit its spread to the environment. Since it is a liquid it can easily penetrate the soil and contaminate groundwater and nearby streams.;Liquid; WetSolid;PEG 400 is a clear, viscous, colourless or almost colourless hygroscopic liquid; PEG 3000, PEG 3350, PEG 4000, PEG 6000 and PEG 8000 are white or almost white solids with a waxy or paraffin-like appearance;Liquid;ODOURLESS COLOURLESS VISCOUS HYGROSCOPIC LIQUID.;COLOURLESS VISCOUS SLIGHTLY HYGROSCOPIC LIQUID.;Clear, colorless, syrupy, odorless liquid.;Clear, colorless, syrupy, odorless liquid. [antifreeze] [Note: A solid below 9°F.];Clear, colorless, syrupy (viscous) liquid at room temperature. Often colored fluorescent yellow-green when used in automotive antifreeze. Group: Polymers. Product ID: ethane-1,2-diol. Molecular formula: 62.07g/mol. Mole weight: (C2H4O)nH2O (n = number of ethylene oxide units corresponding to a molecular weight of 6 000, about 140); HOCH2CH2OH; HO(C2H4O)nH; CH2OHCH2OH; C2H6O2. C(CO)O. InChI=1S/C2H6O2/c3-1-2-4/h3-4H,1-2H2. LYCAIKOWRPUZTN-UHFFFAOYSA-N. | |
| Poly(ethylene glycol) 2-aminoethyl ether biotin | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Bioconjugation, drug delivery, peg hydrogel, crosslinker, surface functionalization. Group: Poly(ethylene glycol) and poly(ethylene oxide). Pack Sizes: Packaging 100 mg in glass insert. Molecular formula: PEG average Mn 3,400 (n~77). | |
| Polyethylene Glycol 400 | Polyethylene glycol as being an addition polymer of ethylene oxide and water. Polyethylene glycol grades 200-600 are liquids; grades 1000 and above are solids at ambient temperatures. Liquid grades (PEG 200-600) occur as clear, colorless or slightly yellow-colored, viscous liquids. They have a slight but characteristic odor and a bitter, slightly burning taste. PEG 600 can occur as a solid at ambient temperatures. Solid grades (PEG>1000) are white or off-white in color, and range in consistency from pastes to waxy flakes. They have a faint, sweet odor. Grades of PEG 6002 and above are available as freeflowing milled powders. Synonyms: Macrogol 400. CAS No. 25322-68-3. Product ID: PE-0475. Molecular formula: HOCH2(CH2OCH2)nCH2OH, n=7~9. Category: Stabilizer; Plasticizer; Base Agents; Coating Agents; Wetting Agents; Emulsifier; Excipient; Collapsing Agents; Solvent; Dissolving aid. Product Keywords: Binder Excipients; Stabilizers; Surfactant Excipients; ; PE-0475; Polyethylene Glycol 400; Stabilizer; Plasticizer; Base Agents; Coating Agents; Wetting Agents; Emulsifier; Excipient; Collapsing Agents; Solvent; Dissolving aid; HOCH2(CH2OCH2)nCH2OH, n=7~9; 25322-68-3. UNII: B697894SGQ. Chemical Name: Polyethylene Glycol 400. Grade: Pharmceutical Excipients. Administration route: Intramuscular injection; Intravenous injection; Nasal spray; Ophthalmic; Topical application; Oral. Dosage Form: Injections, sprays, drop | |
| Polyethylene Glycol 400 | Polyethylene glycol as being an addition polymer of ethylene oxide and water. Polyethylene glycol grades 200-600 are liquids; grades 1000 and above are solids at. ambient temperatures. Liquid grades (PEG 200-600) occur as clear, colorless or slightly yellow-colored, viscous liquids. They have a slight but characteristic odor and a bitter, slightly burning taste. PEG 600 can occur as a solid at ambient temperatures. Solid grades (PEG>1000) are white or off-white in color, and range in consistency from pastes to waxy flakes. They have a faint, sweet odor. Grades of PEG 6003 and above are available as freeflowing milled powders. Synonyms: Macrogol 400. CAS No. 25322-68-3. Product ID: PE-0671. Molecular formula: HOCH2(CH2OCH2)nCH2OH, n=7~9. Category: Stabilizer; surface active agent; plasticizer; slip agent; base agent; adhesive; gloss agent; coating agent; wetting agent; emulsifier; adhesive agent; adhesion enhancer; excipient; ; Collapsing agent; Solvent; Dissolving aid. Product Keywords: Humectants Excipients; PE-0671; Polyethylene Glycol 400; 25322-68-3; Macrogol 400. UNII: B697894SGQ. Chemical Name: Polyethylene Glycol 400. Grade: Pharmaceutical grade. Administration route: Intramuscular injection; Intravenous injection; Nasal spray; Ophthalmic; Topical application; Oral. Dosage Form: Injections, sprays, drops, syrups. Stability and Storage Conditions: Store in airtight container. Commonly used amount and | |
| Polyethylene Glycol 4000 | Polyethylene glycol as being an addition polymer of ethylene oxide and water. Polyethylene glycol grades 200-600 are liquids; grades 1000 and above are solids at ambient temperatures. Liquid grades (PEG 200-600) occur as clear, colorless or slightly yellow-colored, viscous liquids. They have a slight but characteristic odor and a bitter, slightly burning taste. PEG 600 can occur as a solid at ambient temperatures. Solid grades (PEG>1000) are white or off-white in color, and range in consistency from pastes to waxy flakes. They have a faint, sweet odor. Grades of PEG 6002 and above are available as freeflowing milled powders. CAS No. 25322-68-3. Product ID: PE-0440. Category: Stabilizer; Plasticizer; Solvent; Base; Binder; Suspending Agents; Coating Agents; Lubricant; Sugar-Coating Agents; isotonic Agents; Thickener; Excipient; Dispersant; Solvent. Product Keywords: Dispersion Excipients; Stabilizers; Binder Excipients; ; PE-0440; Polyethylene Glycol 4000; Stabilizer; Plasticizer; Solvent; Base; Binder; Suspending Agents; Coating Agents; Lubricant; Sugar-Coating Agents; isotonic Agents; Thickener; Excipient; Dispersant; Solvent; ; 25322-68-3. UNII: 4R4HFI6D95. Chemical Name: Polyethylene glycol 4000. Grade: Pharmceutical Excipients. Administration route: Dental; Intra-articular injection; Intra-synovial injection; Intramuscular injection; Rectal; Sublingual; Topical; Vaginal. Dosage Form: Dental; Intra-arti | |
| Polyethylene Glycol 600 | Ethylene glycol is a clear, colorless syrupy liquid. The primary hazard is the threat to the environment. Immediate steps should be taken to limit its spread to the environment. Since it is a liquid it can easily penetrate the soil and contaminate groundwater and nearby streams.;Liquid; WetSolid;PEG 400 is a clear, viscous, colourless or almost colourless hygroscopic liquid; PEG 3000, PEG 3350, PEG 4000, PEG 6000 and PEG 8000 are white or almost white solids with a waxy or paraffin-like appearance;Liquid;ODOURLESS COLOURLESS VISCOUS HYGROSCOPIC LIQUID.;COLOURLESS VISCOUS SLIGHTLY HYGROSCOPIC LIQUID.;Clear, colorless, syrupy, odorless liquid.;Clear, colorless, syrupy, odorless liquid. [antifreeze] [Note: A solid below 9°F.];Clear, colorless, syrupy (viscous) liquid at room temperature. Often colored fluorescent yellow-green when used in automotive antifreeze. Group: Polymers. Product ID: ethane-1,2-diol. Molecular formula: 62.07g/mol. Mole weight: (C2H4O)nH2O (n = number of ethylene oxide units corresponding to a molecular weight of 6 000, about 140); HOCH2CH2OH; HO(C2H4O)nH; CH2OHCH2OH; C2H6O2. C(CO)O. InChI=1S/C2H6O2/c3-1-2-4/h3-4H,1-2H2. LYCAIKOWRPUZTN-UHFFFAOYSA-N. | |
| Polyethylene Glycol 6000 | Ethylene glycol is a clear, colorless syrupy liquid. The primary hazard is the threat to the environment. Immediate steps should be taken to limit its spread to the environment. Since it is a liquid it can easily penetrate the soil and contaminate groundwater and nearby streams.;Liquid; WetSolid;PEG 400 is a clear, viscous, colourless or almost colourless hygroscopic liquid; PEG 3000, PEG 3350, PEG 4000, PEG 6000 and PEG 8000 are white or almost white solids with a waxy or paraffin-like appearance;Liquid;ODOURLESS COLOURLESS VISCOUS HYGROSCOPIC LIQUID.;COLOURLESS VISCOUS SLIGHTLY HYGROSCOPIC LIQUID.;Clear, colorless, syrupy, odorless liquid.;Clear, colorless, syrupy, odorless liquid. [antifreeze] [Note: A solid below 9°F.];Clear, colorless, syrupy (viscous) liquid at room temperature. Often colored fluorescent yellow-green when used in automotive antifreeze. Group: Polymers. Product ID: ethane-1,2-diol. Molecular formula: 62.07g/mol. Mole weight: (C2H4O)nH2O (n = number of ethylene oxide units corresponding to a molecular weight of 6 000, about 140); HOCH2CH2OH; HO(C2H4O)nH; CH2OHCH2OH; C2H6O2. C(CO)O. InChI=1S/C2H6O2/c3-1-2-4/h3-4H,1-2H2. LYCAIKOWRPUZTN-UHFFFAOYSA-N. | |
| Poly(ethylene glycol), average Mn 400 | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and redu. Group: Polymers. Alternative Names: PEG. CAS No. 25322-68-3. Pack Sizes: Packaging 250, 500 g in poly bottle 20 kg in poly drum 5 g in glass bottle. Molecular formula: Mn 380-420 average Mn 400. C(CO)O. 1S/C2H6O2/c3-1-2-4/h3-4H,1-2H2. LYCAIKOWRPUZTN-UHFFFAOYSA-N. | |
| Poly(ethylene glycol), average Mn 4000 | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Polymers. Alternative Names: PEG. CAS No. 25322-68-3. Pack Sizes: Packaging 5 kg in glass bottle 1 kg in poly bottle. Molecular formula: Mn 3,500-4,500 average Mn 4000. C(CO)O. 1S/C2H6O2/c3-1-2-4/h3-4H,1-2H2. LYCAIKOWRPU | |
| Poly(ethylene glycol) methyl ether azide | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Peg functionalized with azide is commonly used in copper-mediated ligation (click chemistry). peg of this molecular weight should remain amorphous at room temperature. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: Methoxypolyethylene glycol azide, mPEG-N3, azido mPEG, PEG N3, methoxyPEG azide, mPEG azide. CAS No. 89485-61-0. Pack Sizes: Packaging 1 mL in glass bottle. Molecular formula: PEG average Mn 350 (n~8) average Mn 400. | |
| Poly(ethylene glycol) methyl ether-block-poly(ε-caprolactone) | This polymer product is biodegradable. Uses: Biodegradable polymer for drug delivery. Group: Biodegradable polymers. Alternative Names: PEG-PCL, PEG-b-PCL. Pack Sizes: 1 g in glass bottle. Molecular formula: PCL average Mn 25,000 PEG average Mn 5,000 apparent mol wt 20000-30000 (PCL) apparent mol wt 4000-6000 (PEG). Mole weight: CH3(C2H4O)nO(C6H10O2)mH. | |
| Polyethylene Glycol Monoisotridecyl Ether | Polyethylene Glycol Monoisotridecyl Ether. Group: Biochemicals. Alternative Names: α-Isotridecyl-ω-hydroxypoly(oxy-1,2-ethanediyl); Arlypon IT 10; Berol 048; Dehscoxid 732; Ethox 2400; Ethox TDA 9; Ethoxylated isotridecanol; Ethoxylated Isotridecyl Alcohol; Eusapon S; Exxal F 5716; Genapol V 4739; Genapol X; Gezetol 138; Imbentin T 050; Isotridecanol Ethoxylate; Isotrideceth 15; Leocol TD 120; Leocol TD 150; Leocol TD 50; Leocol TD 90; Leocol TDA 400-75; Lutensol TO 10; ; M 0-7; M 0-9; Marlipal 013/40; Marlosol TA 3050; Marlosol TA 3090; Nissan Dispanol TOC; Noigen TDS 200D; Noigen TDS 80; Novanit MA; Novel II TDA 8.5; Novel II TDA 9; Novel II TDA 9.5; PEG isotridecyl ether; Polyethylene glycol isotridecyl ether; Polyethylene Glycol Isotridecyl Monoether; Polyethylene Glycol Monoether with isotridecyl alcohol; Polyethylene Glycol Monoisotridecyl ether; Polyoxyethylene isotridecyl ether; Rhodasurf ROX; Rhodasurf TR 15-40; Rhodasurf TR 25-25; Rokanol IT; Surfonic TDA 11; Surfonic TDA 15/88; Surfonic TDA 3; Surfonic TDA 8; Surfonic TDA 9; Synperonic 13/10; Synperonic 13/6.5; T-DET A 134; TA 400; Tego Alkanol TD 6; Unitol IT 140; Villa 51; Walloxen TR 100; Walloxen TR 16; X 1005. Grades: Highly Purified. CAS No. 9043-30-5. Pack Sizes: 10g. Molecular Formula: C13H28O (C2 H4O)n. US Biological Life Sciences. | Worldwide |
| Poly(ethylene glycol) [N-(2-maleimidoethyl)carbamoyl]methyl ether 2-(biotinylamino)ethane | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and redu. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: Biotin-PEG, Biotin polyoxyethylene maleimide, Biotin-PEG-maleimide, Biotinylated PEG. Pack Sizes: Packaging 100 mg in glass insert. Molecular formula: PEG average Mn 5000 (n~110) average Mn 5,400. | |
| Poly(Ethylene Glycol) (N) Distearate | Poly(Ethylene Glycol) (N) Distearate. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: POLY(ETHYLENE GLYCOL) (N) DISTEARATE; POLY(ETHYLENE GLYCOL) DISTEARATE; POLYETHYLENE GLYCOL 6000 DISTEARATE; POLYETHYLENE GLYCOL 400 DISTEARATE; PEG 600 DISTEARATE; PEG 6000 DISTEARATE; PEG 4000 DISTEARATE; PEG 400 DISTEARATE. CAS No. 9005-8-7. Molecular formula: 639.039978027344. Mole weight: C40< / sub>H78< / sub>O5< / sub>. | |
| Polythylene Glycol 1000 (PEG 1000) | Polythylene Glycol 1000 (PEG 1000). Group: Biochemicals. Alternative Names: Polyethylene Glycols; 1,2-Ethanediol Homopolymer; 1660O; 1660S; 400DAB8; Alcox L 11; Alkox; Antarox E 4000; Aqua Calk TWB-P; Aquacide III; Aquaffin; B 22181; BDH 301; Badimol; Beraid 3540; Bradsyn PEG; Breox CAFO 154; CBP 20; CO 1006; Carbowax; PEG 8000; Cartaretin E; Cerasol 200A; Cerasol 250A; Chemiox E 20(C); Colonsoft; DB-WAX; DD 3002; Deactivator H; Decuflux RM 33; Desmophen L 1208; DuraSeal (tissue sealant); Duraseal; Emkapol 150; Emkapol 200; Emkapol 4200; Ethylene Glycol Homopolymer; Ethylene Glycol Polymer; Ethylene Oxide Polymer; FPR; FPR (polyether); Feltmaster 15LF; Floc 999; Flocc 999; Fomrez PEG 1000L; Forlax; G 3350; GPE 1000; GPE 400; Gafanol E 200; Gafanol E 300; Genoplast 200; Gligogum 4000; GlycoLax; H 22; HM 500; HPEO 4250; IW; IW (dispersant); Isocolan; KPEG 6000; KPEG 6000LA; KleanPrep; Kollisolv PEG 300; Kollisolv PEG 400; L 300; L 6; Lanogene C; Laprol 1001; Lineartop P; Lipoxol 2000; Lumulse PEG 200; Lutrol E 300; M 2000H; M 3686B; M 9000; M-LE 1013; MN 300; Macol E 300; Macrogol;Maxifloc 998; Maxifloc 999; Meisei 4000; Microsolv PEG 100; MiraLax; Modopeg; Modopeg 4000; Monopol PEG 200; N 80NF; Netbond FRA; Newfrontier PEM 3. Grades: Highly Purified. CAS No. 25322-68-3. Pack Sizes: 1g. Molecular Formula: (C2H4O)nH2O. US Biological Life Sciences. | Worldwide |
| Polythylene Glycol 200 (PEG 200) | Polythylene Glycol 200 (PEG 200). Group: Biochemicals. Alternative Names: Polyethylene Glycols; 1,2-Ethanediol Homopolymer; 1660O; 1660S; 400DAB8; Alcox L 11; Alkox; Antarox E 4000; Aqua Calk TWB-P; Aquacide III; Aquaffin; B 22181; BDH 301; Badimol; Beraid 3540; Bradsyn PEG; Breox CAFO 154; CBP 20; CO 1006; Carbowax; PEG 8000; Cartaretin E; Cerasol 200A; Cerasol 250A; Chemiox E 20(C); Colonsoft; DB-WAX; DD 3002; Deactivator H; Decuflux RM 33; Desmophen L 1208; DuraSeal (tissue sealant); Duraseal; Emkapol 150; Emkapol 200; Emkapol 4200; Ethylene Glycol Homopolymer; Ethylene Glycol Polymer; Ethylene Oxide Polymer; FPR; FPR (polyether); Feltmaster 15LF; Floc 999; Flocc 999; Fomrez PEG 1000L; Forlax; G 3350; GPE 1000; GPE 400; Gafanol E 200; Gafanol E 300; Genoplast 200; Gligogum 4000; GlycoLax; H 22; HM 500; HPEO 4250; IW; IW (dispersant); Isocolan; KPEG 6000; KPEG 6000LA; KleanPrep; Kollisolv PEG 300; Kollisolv PEG 400; L 300; L 6; Lanogene C; Laprol 1001; Lineartop P; Lipoxol 2000; Lumulse PEG 200; Lutrol E 300; M 2000H; M 3686B; M 9000; M-LE 1013; MN 300; Macol E 300; Macrogol;Maxifloc 998; Maxifloc 999; Meisei 4000; Microsolv PEG 100; MiraLax; Modopeg; Modopeg 4000; Monopol PEG 200; N 80NF; Netbond FRA; Newfrontier PEM 300; . Grades: Highly Purified. CAS No. 25322-68-3. Pack Sizes: 1g. Molecular Formula: (C2H4O)nH2O. US Biological Life Sciences. | Worldwide |
| Y-(mPEG10K)2-(PEG20k-NH2) | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Molecular formula: average Mn 40000. | |
| Y-PEG40K-Acetaldehyde | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: Y-PEG-Acetaldehyde. Molecular formula: average Mn 40000. | |
| Y-PEG40K-COOH | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: Y-PEG-COOH. Molecular formula: average Mn 40000. | |
| Y-PEG40K-Fluorescein | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Molecular formula: average Mn 40000. ≥95%. | |
| Y-PEG40K-MAL | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: Y-PEG-MAL. Molecular formula: average Mn 40000. | |
| Y-PEG40K-NH2 | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: Y-shape PEG Amine, Y-PEG-NH2. Molecular formula: average Mn 40000. | |
| Y-PEG40K-NHS | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: Y-PEG-NHS. Molecular formula: average Mn 40000. | |
| Y-PEG40K-Propionaldehyde | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: Y-PEG-Propionaldehyde. Molecular formula: average Mn 40000. | |
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