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| Product | Description | |
|---|---|---|
| Poly(ethylene-co-acrylic acid), acrylic acid 15 wt. % | Forms reversible ionic clusters (crosslinks). Promotes adhesion to various substrates, tougher, more chemically resistant and more transparent than parent acid copolymer. Uses: Processing and performance additive. promotes crystallization of pet. assists dispersion of additives in plastics. Group: Acrylics. CAS No. 9010-77-9. Molecular formula: (CH2CH2)x[CH2CH(CO2H)]y. Canonical SMILES: C=C.OC(=O)C=C. Density: 0.93 g/mL at 25 °C. Catalog: ACM9010779. |  |
| Poly(ethylene-co-acrylic acid) zinc salt | Poly(ethylene-co-acrylic acid) zinc salt. Group: Hydrophobic polymers. CAS No. 28208-80-2. Product ID: zinc; ethene; prop-2-enoate. Molecular formula: 235.5g/mol. Mole weight: C8H10O4Zn. C=C.C=CC(=O)[O-].C=CC(=O)[O-].[Zn+2]. InChI=1S/2C3H4O2. C2H4. Zn/c2*1-2-3(4)5; 1-2; /h2*2H, 1H2, (H, 4, 5); 1-2H2; /q; ; ; +2/p-2. HENHBQJZXRPLOX-UHFFFAOYSA-L. |  |
| Acrylamide-13C3 | Acrylamide-13C3. Group: Biochemicals. Alternative Names: 2-Propenamide-13C3; Acrylic Amide-13C3; Bio-Acrylamide 50-13C3; Ethylenecarboxamide; NSC 7785-13C3; Propenamide; Vinyl Amide-13C3. Grades: Highly Purified. CAS No. 287399-26-2. Pack Sizes: 1mg. Molecular Formula: 13C3H5NO, Molecular Weight: 74.06. US Biological Life Sciences. |  Worldwide |
| Acrylamide, 99.9+% for Molecular Biology | Used as chemical intermediate in production of polyacrylamides, for use in protein electrophoresis (PAGE), synthesis of dyes and copolymers for contact lenses. Group: Biochemicals. Alternative Names: 2-Propenamide; Acrylic Amide; Bio-Acrylamide 50; Ethylenecarboxamide; NSC 7785; Propenamide; Vinyl Amide. Grades: Molecular Biology Grade. CAS No. 79-06-1. Pack Sizes: 1Kg. US Biological Life Sciences. | Worldwide |
| Acrylamide-d3 | Used as chemical intermediate in production of polyacrylamides, for use in protein electrophoresis (PAGE), synthesis of dyes and copolymers for contact lenses. It is reasonably anticipated to be a human carcinogen. Group: Biochemicals. Alternative Names: 2-Propenamide-d3; Acrylic Amide-d3; Bio-Acrylamide 50-d3; Ethylenecarboxamide-d3; NSC 7785-d3; Propenamide-d3; Vinyl Amide-d3. Grades: Highly Purified. CAS No. 122775-19-3. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Triethylene Glycol Dimethacrylate (Stabilized with MEHQ) | Esters of acrylic acid and methacrylic acid, more commonly known as acrylates and methacrylates are key raw materials in the coatings and printing industry, and in food packaging. Group: Biochemicals. Alternative Names: 2-Methyl-2-propenoic Acid 1,1'-[1,2-ethanediylbis(oxy-2,1-ethanediyl)] Ester; Methacrylic Acid Ethylenebis (oxyethylene) Ester; 1, 2-Bis[2- (methacryloyloxy) ethoxy]ethane; ATM 2; Acryester 3ED; Bisomer TEGDMA; Blemmer PDE 150; EM 328; Esschem 943X7469; Ethylenebis (oxyethylene) methacrylate; NSC 84260; Neomer PM 201; SR 205; Sartomer SR 205; TEDMA; TEGDMA; TGM 3; TGM 3S. Grades: Highly Purified. CAS No. 109-16-0. Pack Sizes: 25g. US Biological Life Sciences. | Worldwide |
| 2-[2-[4-[2-[4-[2-(2-Prop-2-enoyloxyethoxy)ethoxy]phenyl]propan-2-yl]phenoxy]ethoxy]ethyl prop-2-enoate | Heterocyclic Organic Compound. Alternative Names: propane-2,2-diylbis(benzene-4,1-diyloxyethane-2,1-diyloxyethane-2,1-diyl) bisprop-2-enoate, AC1L3MVJ, AC1Q68FA, SureCN6292051, CTK5A5039, EINECS 260-130-0, AR-1L2176, AG-F-97896, 110199-80-9, 2-[2-[4-[2-[4-[2-(2-prop-2-enoyloxyethoxy)ethoxy]phenyl]propan-2-yl]phenoxy]ethoxy]ethyl prop-2-enoate, 2-Propenoic acid, (1-methylethylidene)bis(4,1-phenyleneoxy-2,1-ethanediyloxy-2,1-ethanediyl) ester, 2-Propenoic acid, 1,1-((1-methylethylidene)bis(4,1-phenyleneoxy-2,1-ethanediyloxy-2,1-ethanediyl)) ester, 2-Propenoic acid,1,1-[(1-methylethylidene)bis(4,1-phenyleneoxy-2,1-ethanediyloxy-2,1-ethanediyl)]ester, 2-Propenoicacid, (1-methylethylidene)bis(4,1-phenyleneoxy-2,1-ethanediyloxy-2,1-ethanediyl)ester (9CI); 2, 2-Bis (4-acryloxyethoxyethoxyphenyl)propane; 2, 2-Bis (4-acryloyloxydiethoxyphenyl)propane; 2, 2-Bis[4-acryloyloxydi (ethyleneoxy)phenyl]propane; A-BPE 4; Aronix TO 1437;Beam Set 750; Bisphenol A diethylene glycol diacrylate; NK Ester A-BPE 4, 460357-43-1, 53988-31-1. CAS No. 110199-80-9. Molecular formula: C29H36O8. Mole weight: 512.591 g/mol. Purity: 0.96. IUPACName: 2-[2-[4-[2-[4-[2-(2-prop-2-enoyloxyethoxy)ethoxy]phenyl]propan-2-yl]phenoxy]ethoxy]ethyl prop-2-enoate. Canonical SMILES: CC (C) (C1=CC=C (C=C1)OCCOCCOC (=O)C=C)C2=CC=C (C=C2)OCCOCCOC (=O)C=C. Catalog: ACM110199809. | |
| 2-(2-ethoxyethoxy)ethyl prop-2-enoate | Heterocyclic Organic Compound. Alternative Names: 2-(2-Ethoxyethoxy)ethyl acrylate, Carbitol acrylate, 7328-17-8, 2-(2-ethoxyethoxy)ethyl prop-2-enoate, Di(ethylene glycol) ethyl ether acrylate, 2-Propenoic acid, 2-(2-ethoxyethoxy)ethyl ester, EINECS 230-811-7, 102484-00-4, AC1Q68FC, DSSTox_CID_24983, DSSTox_RID_80632, DSSTox_GSID_44983, 408298_ALDRICH, 2-(2-Ethoxyethoxy)ethylacrylate, CTK5D7723, FTALTLPZDVFJSS-UHFFFAOYSA-, AC1L3218, Tox21_301618, ANW-42292, AR-1C6707. CAS No. 102484-00-4. Molecular formula: C9H16O4. Mole weight: 188.221 g/mol. Purity: 0.96. IUPACName: 2-(2-ethoxyethoxy)ethyl prop-2-enoate. Catalog: ACM102484004. | |
| 2,3-Bis(2,6-diisopropylphenylimino)butane | 1. Ligand used in the preparation of highly active metal catalysts for the polymerization of ethylene (ref 1, M=Ni, Pd) and olefins (ref 2, M=Pd; ref 3, M= Hf, Zr) Ligand for the iron catalyzed polymerization of styrene acrylate monomers Ligand for Yttrium complex that catalysis the ring-opening polymerization of cyclic esters Ligand for rare-earth dichloro and bis(alkyl) complexes for isoprene polymerization Ligand for cobalt catalyzed alkene hydroboration Ligand for nickel catalyzed alkene hydrosilylation. Group: Heterocyclic organic compound. Alternative Names: N-(2,6-diisopropylphenyl)-N-{2-[(2,6-diisopropylphenyl)imino]-1-methylpropylidene}amine; N-((E,2E)-2-[(2,6-Diisopropylphenyl)imino]-1-methylpropylidene)-2,6-diisopropylaniline #; TRA0127768; N,N inverted exclamation marka-Bis(2,6-diisopropylphenyl)-2,3-butanediimine; J-400165; AKOS025295710; N2,N3-bis[2,6-di(propan-2-yl)phenyl]butane-2,3-diimine; (N,N'E,N,N'E)-N,N'-(butane-2,3-diylidene)bis(2,6-diisopropylaniline); 74663-77-7; ZINC15230312. CAS No. 74663-77-7. Molecular formula: C28H40N2. Mole weight: 404.642g/mol. IUPACName: 2-N,3-N-bis[2,6-di(propan-2-yl)phenyl]butane-2,3-diimine. Canonical SMILES: CC (C)C1=C (C (=CC=C1)C (C)C)N=C (C)C (=NC2=C (C=CC=C2C (C)C)C (C)C)C. Catalog: ACM74663777. | |
| 2-Hydroxyethyl acrylate | Used in the radiation curing system in active diluents and crosslinking agent, can also be as crosslinking agent of resin, plastic, rubber modifier. Group: Other plating chemicals. Alternative Names: HEA;Ethylene glycol monoacrylate. CAS No. 818-61-1. Molecular formula: C5H8O3. Mole weight: 116.12. Appearance: Colorless transparent liquid. Catalog: ACEP818611. | |
| 4arm-PEG10K-Acrylate | 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: 3d printing materials poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: 4arm-PEG-Acrylate, 4arm-PEG-ACLT. Molecular formula: average Mn 10000. | |
| 4arm-PEG20K-Acrylate | 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: 3d printing materials poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: 4arm-PEG-Acrylate, 4arm-PEG-ACLT. Molecular formula: average Mn 20000. | |
| 4-Chlorostyrene | 4-Chlorostyrene is a para-halogenated styrene derivative. It undergoes graft copolymerization with acrylonitrile (AN) onto ethylene-propylene-diene terpolymer (EPDM) in the presence of benzoyl peroxide (initiator). Uses: 4-chlorostyrene was used in the following studies: study of chemical and biochemical properties of the vinyl group of styrene by the development of structure activity relationships (sar). preparation of new bis(pyrazolyl)borato olefin complexes of copper(I). to investigate the regioselectivity in the cationic heck reaction of 4-substituted styrenes. Group: Monomers. CAS No. 1073-67-2. Pack Sizes: Packaging 10, 50 g in glass bottle. Product ID: 1-chloro-4-ethenylbenzene. Molecular formula: 138.59. Mole weight: H2C=CHC6H4Cl. Clc1ccc(C=C)cc1. 1S/C8H7Cl/c1-2-7-3-5-8 (9)6-4-7/h2-6H, 1H2. KTZVZZJJVJQZHV-UHFFFAOYSA-N. | |
| 8arm-PEG10K-Acrylate | 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 10000. | |
| 8arm-PEG10K-Acrylate, tripentaerythritol core | 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: 3d printing materials poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: 8arm-PEG-ACLT, 8arm-PEG-Acrylate, tripentaerythritol core. Molecular formula: average Mn 10000. | |
| 8-arm PEG10K-PCL2K-Acrylate | 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). | |
| 8-arm PEG10K-PLA2K-Acrylate | 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). | |
| 8arm-PEG20K-Acrylate | 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-Acrylate, hexaglycerol core. Molecular formula: average Mn 20000. | |
| 8arm-PEG20K-Acrylate, hexaglycerol core | 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: 3d printing materials poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: 8arm-PEG-Acrylate, hexaglycerol core. Molecular formula: average Mn 20000. | |
| 8-arm PEG5K-Acrylate (hexaglycerol core) | 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 5000. | |
| 8-arm PEG5K-Acrylate (tripentaerythritol core) | 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 5000. | |
| 8-arm PEG5K-PCL1K-Acrylate | 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). | |
| 8-arm PEG5K-PLA1K-Acrylate | 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). ≥95%. | |
| Acrylate-PEG2K-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: Acrylate-PEG-NHS. Molecular formula: average Mn 2000. | |
| Acrylate-PEG3500-Acrylate | 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: Acrylate-PEG-Acrylate, ACLT-PEG-ACLT. Molecular formula: average Mn 3500. | |
| Acrylate-PEG3500-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: Acrylate-PEG-NHS. Molecular formula: average Mn 3,500. | |
| Acrylate-PEG5K-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: Acrylate-PEG-NHS. Molecular formula: average Mn 5000. | |
| Acrylate-PEG7500-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: Acrylate-PEG-NHS. Molecular formula: average Mn 7,500. | |
| Acryloxy Terminated Ethyleneoxide Dimethylsiloxane-Ethyleneoxide Abablock Copolymer, 80 - 120 cSt | Silicone Polymers. Alternative Names: Acryloxy Terminated Polydimethylsiloxane Poly(Dimethylsiloxane), Hydroxypropyl Terminated, Diether With Polyethylene Glycol Monoacrylate Siloxanes And Silicones, Dimethyl, 3-Hydroxypropyl Group-Terminated, Diethers Wth Polyethylene Glycol Monoacrylate. CAS No. 117440-21-8. Mole weight: 520.8g/mol. Appearance: Amber Clear liquid. Catalog: ACM117440218. | |
| Di(ethylene glycol)2-ethylhexyl ether acrylate | Polymer/Macromolecule. Alternative Names: DI(ETHYLENE GLYCOL) 2-ETHYLHEXYL ETHER ACRYLATE;2-ETHYL HEXYL DIGLYCOL ACRYLATE. CAS No. 117646-83-0. Molecular formula: C15H28O4. Mole weight: 272.38. Catalog: ACM117646830. | |
| Di(ethylene glycol) ethyl ether acrylate | Liquid;Liquid. Uses: This product is suitable for scientific research. Group: Monomers. Alternative Names: 2-(2-Ethoxyethoxy)ethyl acrylate. CAS No. 7328-17-8. Product ID: 2-(2-ethoxyethoxy)ethyl prop-2-enoate. Molecular formula: 188.22. Mole weight: H2C=CHCO2(CH2CH2O)2C2H5. CCOCCOCCOC(=O)C=C. 1S/C9H16O4/c1-3-9 (10)13-8-7-12-6-5-11-4-2/h3H, 1, 4-8H2, 2H3. FTALTLPZDVFJSS-UHFFFAOYSA-N. ≥ 97%. | |
| Di(ethylene glycol) ethyl ether acrylate, 90%(GC), contains 1000 ppm MEHQ as stabilizer | Liquid;Liquid. Group: Monomers. CAS No. 7328-17-8. Product ID: 2-(2-ethoxyethoxy)ethyl prop-2-enoate. Molecular formula: 188.22g/mol. Mole weight: C9H16O4. CCOCCOCCOC(=O)C=C. InChI=1S/C9H16O4/c1-3-9 (10)13-8-7-12-6-5-11-4-2/h3H, 1, 4-8H2, 2H3. FTALTLPZDVFJSS-UHFFFAOYSA-N. | |
| EDTA-C2-dT-CE Phosphoramidite | EDTA-C2-dT-CE Phosphoramidite, a catalyst for biomedical synthesis, is rich in EDTA, ensuring thorough metal ion chelation. Its enhanced stability and selectivity imply potential applications in disease research, including HIV and cancer. Employed mostly in genome editing, it exhibits profound biomedical value through its performance in the synthesis of trace oligonucleotides. Synonyms: 5'-Dimethoxytrityl-5-[N-ethylenediaminetriethylacetate, monoacetylaminoethyl-3-acrylimido]-2'-deoxyUridine, 3'-[(2-cyanoethyl)-(N,N-diisopropyl)]-phosphoramidite. Molecular formula: C60H81N8O16P. Mole weight: 1201.32. |  |
| Ethylene acrylate | Heterocyclic Organic Compound. CAS No. 111802-12-1. Molecular formula: C8H10O4. Mole weight: 170.17. Catalog: ACM111802121. | |
| ethylene/ethyl acrylate copolymer | Liquid. Group: Polymers. CAS No. 9010-86-0. Product ID: ethene; ethyl prop-2-enoate. Molecular formula: 128.17g/mol. Mole weight: C7H12O2. CCOC(=O)C=C.C=C. InChI=1S/C5H8O2.C2H4/c1-3-5(6)7-4-2; 1-2/h3H, 1, 4H2, 2H3; 1-2H2. CGPRUXZTHGTMKW-UHFFFAOYSA-N. | |
| Ethylene-Ethyl Acrylate Copolymer (82/18) | Ethylene-Ethyl Acrylate Copolymer (82/18). CAS No. 9010-86-0. |  CA, FL & NJ |
| Ethylene glycol methyl ether acrylate | 2-methoxyethyl acrylate can undergo RAFT copolymerization with itaconic anhydride. Uses: This product is suitable for scientific research. Group: Monomers. Alternative Names: 2-Methoxyethyl acrylate. CAS No. 3121-61-7. Pack Sizes: Packaging 1 L in glass bottle 250 mL in glass bottle. Product ID: 2-methoxyethyl prop-2-enoate. Molecular formula: 130.14. Mole weight: H2C=CHCO2CH2CH2OCH3. COCCOC(=O)C=C. 1S/C6H10O3/c1-3-6(7)9-5-4-8-2/h3H, 1, 4-5H2, 2H3. HFCUBKYHMMPGBY-UHFFFAOYSA-N. | |
| Ethylene glycol methyl ether acrylate | Ethylene glycol methyl ether acrylate. Group: Biochemicals. Grades: Highly Purified. CAS No. 3121-61-7. Pack Sizes: 250g, 500g, 1kg, 2Kg, 5Kg. Molecular Formula: C6H10O3. US Biological Life Sciences. | Worldwide |
| Ethylene glycol methyl ether acrylate, 98% | 2-methoxyethyl acrylate is a clear colorless liquid with a sharp musty odor. (NTP, 1992);Liquid. Group: Monomers. CAS No. 3121-61-7. Product ID: 2-methoxyethyl prop-2-enoate. Molecular formula: 130.14g/mol. Mole weight: C6H10O3. COCCOC(=O)C=C. InChI=1S/C6H10O3/c1-3-6 (7)9-5-4-8-2/h3H, 1, 4-5H2, 2H3. HFCUBKYHMMPGBY-UHFFFAOYSA-N. | |
| Ethylene glycol monoethyl ether acrylate | Heterocyclic Organic Compound. Alternative Names: 2-ethoxy-ethanoacrylate;2-Ethoxyethyl 2-propenoate;2-ethoxyethyl-2-propenoate;2-Ethoxyethylester kyseliny akrylove; 2-ethoxyethylesterkyselinyakrylove; 2-ethoxyethylesterkyselinyakrylove (czech); 2-Propenoic acid, 2-ethoxyethyl ester;2-propenoicacid,2-ethoxy. CAS No. 106-74-1. Molecular formula: C7H12O3. Mole weight: 144.17. Density: 0.982. Catalog: ACM106741. | |
| Ethylene glycol phenyl ether acrylate | Ethylene glycol phenyl ether acrylate (PA) is a monofunctional acrylate. Uses: Ethylene glycol phenyl ether acrylate (pa) monomer may be used to fabricate polymerization induced grating pattern on photopolymer films. Group: Monomers. Alternative Names: 2-Phenoxyethyl acrylate. CAS No. 48145-04-6. Pack Sizes: Packaging 250 mL in poly bottle 1 L in poly bottle. Product ID: 2-phenoxyethyl prop-2-enoate. Molecular formula: 192.21. Mole weight: H2C=CHCO2CH2CH2OC6H5. C=CC(=O)OCCOc1ccccc1. 1S/C11H12O3/c1-2-11 (12)14-9-8-13-10-6-4-3-5-7-10/h2-7H, 1, 8-9H2. RZVINYQDSSQUKO-UHFFFAOYSA-N. | |
| Ethylene glycol phenyl ether acrylate, 90%, contains 100ppm hydroquinone as inhibitor | DryPowder; Liquid. Group: Monomers. CAS No. 48145-04-6. Product ID: 2-phenoxyethyl prop-2-enoate. Molecular formula: 192.21g/mol. Mole weight: C11H12O3. C=CC(=O)OCCOC1=CC=CC=C1. InChI=1S/C11H12O3/c1-2-11 (12)14-9-8-13-10-6-4-3-5-7-10/h2-7H, 1, 8-9H2. RZVINYQDSSQUKO-UHFFFAOYSA-N. | |
| Ethylene Methyl Acrylate | Ethylene Methyl Acrylate. Group: Polymers. | |
| mPEG12-Acrylate | 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). | |
| mPEG5-Acrylate | 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). | |
| mPEG6-Acrylate | 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). | |
| mPEG7-Acrylate | 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). | |
| N,N'-Ethylenebis(acrylamide) | N,N'-Ethylenebis(acrylamide). Uses: This product is suitable for scientific research. Group: Monomers. Alternative Names: N,N'-Dimethylenebis(acrylamide), N,N'-Bisacryloyl-1,2-diaminoethane. CAS No. 2956-58-3. Product ID: N-[2-(prop-2-enoylamino)ethyl]prop-2-enamide. Molecular formula: 168.19. Mole weight: (H2C=CHCONHCH2-)2. C=CC(=O)NCCNC(=O)C=C. 1S/C8H12N2O2/c1-3-7 (11)9-5-6-10-8 (12)4-2/h3-4H, 1-2, 5-6H2, (H, 9, 11) (H, 10, 12). AYGYHGXUJBFUJU-UHFFFAOYSA-N. | |
| Perylene | Perylene molecules are fluorescent in nature. Ultraviolet photoemission spectroscopy and low energy electron diffraction of the structure of 4Å thick perylene dye layers adsorbed on the surface of Ru (0001) has been investigated. Uses: Perylene was used in the fabrication of gold nanoparticle (aunp) : poly(ethylene oxide) (peo) nanocomposite thin films. perylene nanoparticles doped into poly(acrylonitrile) (pan) were used to monitor the temperature change caused due to the nanoparticle plasmon-mediated heating within the polymer fibres and films. ordered epitaxial perylene films may be used to fabricate a multilayered electroluminescent device. Group: Carbon nano materials molecular conductorsorganic light-emitting diode (oled) materials other electronic materials sublimed materials. Alternative Names: peri-Dinaphthalene. CAS No. 198-55-0. Pack Sizes: 1, 5 g in glass bottle. Product ID: Perylene. Molecular formula: 252.3. Mole weight: C20H12. C1=CC2=C3C (=C1)C4=CC=CC5=C4C (=CC=C5)C3=CC=C2. InChI= 1S / C20H12 / c1-5-13-6-2-11-17-18-12-4-8-14-7-3-10 -16 (20 (14) 18) 15 (9-1) 19 (13) 17 / h1-12H. CSHWQDPOILHKBI-UHFFFAOYSA-N. 95%+. | |
| Perylene | Perylene molecules are fluorescent in nature. Ultraviolet photoemission spectroscopy and low energy electron diffraction of the structure of 4Å thick perylene dye layers adsorbed on the surface of Ru (0001) has been investigated. Uses: Perylene was used in the fabrication of gold nanoparticle (aunp) : poly(ethylene oxide) (peo) nanocomposite thin films. perylene nanoparticles doped into poly(acrylonitrile) (pan) were used to monitor the temperature change caused due to the nanoparticle plasmon-mediated heating within the polymer fibres and films. ordered epitaxial perylene films may be used to fabricate a multilayered electroluminescent device. Group: Organic light emitting diode (oled). Alternative Names: Perylene. CAS No. 198-55-0. Molecular formula: C20H12. Mole weight: 252.31 g/mol. Purity: 95%+. IUPACName: Perylene. Canonical SMILES: C1=CC2=C3C (=C1)C4=CC=CC5=C4C (=CC=C5)C3=CC=C2. Density: 1.35 g/ml. ECNumber: 205-900-9. Catalog: ACM198550. | |
| Poly(ethylene-co-ethyl acrylate) | The polymer product is a hydrophobic material that is insoluble in water or other polar solvents. Uses: Our hydrophobic polymers are used as coatings, adhesives, fibers, films and engineering plastics. furthermore, they are widely used as biomedical polymers for vascular grafts, implants and ophthalmic applications. Group: Hydrophobic polymers. CAS No. 9010-86-0. Product ID: ethene; ethyl prop-2-enoate. Molecular formula: 128.17g/mol. Mole weight: (CH2CH2)x[CH2CH(CO2C2H5)]y. C=C.CCOC(=O)C=C. 1S/C5H8O2.C2H4/c1-3-5(6)7-4-2; 1-2/h3H, 1, 4H2, 2H3; 1-2H2. CGPRUXZTHGTMKW-UHFFFAOYSA-N. | |
| Poly(ethylene-co-methyl acrylate-co-glycidyl methacrylate) | Cross-linkable coatings and adhesion promoter. Group: Biomaterials. Alternative Names: Ethylene-methyl acrylate-glycidyl methacrylate copolymer,Glycidyl methacrylate-ethylene-methyl acrylate copolymer. CAS No. 51541-08-3. Molecular formula: C13H20O5. Mole weight: 256.29g/mol. IUPACName: ethene;methyl prop-2-enoate;oxiran-2-ylmethyl 2-methylprop-2-enoate. Canonical SMILES: CC(=C)C(=O)OCC1CO1.COC(=O)C=C.C=C. Catalog: ACM51541083. | |
| Poly(ethylene-co-methyl acrylate-co-glycidyl methacrylate) | Poly(ethylene-co-methyl acrylate-co-glycidyl methacrylate). Uses: Cross-linkable coatings and adhesion promoter. Group: Hydrophobic polymersself assembly and lithography. Alternative Names: Ethylene-methyl acrylate-glycidyl methacrylate copolymer,Glycidyl methacrylate-ethylene-methyl acrylate copolymer. CAS No. 51541-08-3. Pack Sizes: 250 g in poly bottle. Product ID: ethene; methyl prop-2-enoate; oxiran-2-ylmethyl 2-methylprop-2-enoate. Molecular formula: 256.29g/mol. Mole weight: C13H20O5. CC(=C)C(=O)OCC1CO1.COC(=O)C=C.C=C. 1S/C7H10O3. C4H6O2. C2H4/c1-5(2)7(8)10-4-6-3-9-6; 1-3-4(5)6-2; 1-2/h6H, 1, 3-4H2, 2H3; 3H, 1H2, 2H3; 1-2H2. CNJPFZOQZWIGIB-UHFFFAOYSA-N. | |
| Poly(ethylene glycol)behenyl ether methacrylate | Polymer/Macromolecule. Alternative Names: 18_22-alkylethers;2-ethanediyl),alpha-(2-methyl-1-oxo-2-propenyl)-omega-hydroxy-poly(oxy-c;POLY(ETHYLENE GLYCOL) BEHENYL ETHER METHACRYLATE;Poly(ethylene glycol) behenyl ether methacrylate solution;POLY(ETHYLENE GLYCOL) BEHENYL ETHER METH -ACRYLATE,50 WT%. CAS No. 125441-87-4. Molecular formula: H2C=C(CH3)CO2(CH2CH2O)n(CH2)21CH3. Catalog: ACM125441874. | |
| Poly(ethylene glycol) methyl ether acrylate | 2-methoxyethyl acrylate is a clear colorless liquid with a sharp musty odor. (NTP, 1992);Liquid. Group: Poly(ethylene glycol) and poly(ethylene oxide)polymers. CAS No. 32171-39-4. Product ID: 2-methoxyethyl prop-2-enoate. Molecular formula: 130.14g/mol. Mole weight: C6H10O3. COCCOC(=O)C=C. InChI=1S/C6H10O3/c1-3-6 (7)9-5-4-8-2/h3H, 1, 4-5H2, 2H3. HFCUBKYHMMPGBY-UHFFFAOYSA-N. | |
| Poly(ethylene glycol) phenyl ether acrylate | 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: Ethoxylated phenyl acrylate, Phenol ethoxylate acrylate. CAS No. 56641-05-5. Pack Sizes: Packaging 100 mL in poly bottle. Product ID: 2-phenoxyethyl prop-2-enoate. Molecular formula: average Mn 324. Mole weight: C11H12O3. C=CC(=O)OCCOCCOc1ccccc1. 1S/C11H12O3/c1-2-11 (12)14-9-8-13-10-6-4-3-5-7-10/h2-7H, 1, 8-9H2. RZVINYQDSSQUKO-UHFFFAOYSA-N. | |
| Tetraethylene glycol | An oligomer of polyethylene glycol, tetra (ethylene glycol) (TEG) is a transparent, colorless, odorless, low volatility, hygroscopic liquid soluble in ethyl alcohol and very soluble in water. Uses: Used for the synthesis of tetraethylene glycol metha acrylate monomer. glow discharge plasma deposition of teg renders surfaces resistant to protein adsorption and cellular attachment. Group: Poly(ethylene glycol) and poly(ethylene oxide)polymers. Alternative Names: Bis[2-(2-hydroxyethoxy)ethyl] ether, Tetraglycol, Tetra(ethylene glycol). CAS No. 112-60-7. Pack Sizes: Packaging 100 g in poly bottle 20 kg in steel drum 1, 3 kg in poly bottle. Product ID: 2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethanol. Molecular formula: 194.23, average Mn 200. Mole weight: C8H18O5. OCCOCCOCCOCCO. 1S / C8H18O5 / c9-1-3-11-5-7-13-8-6-12-4-2-10 / h9-10H, 1-8H2. UWHCKJMYHZGTIT-UHFFFAOYSA-N. | |
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