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| Product | Description | |
|---|---|---|
| poly(ethyl acrylate) | Ethyl acrylate, stabilized appears as a clear colorless liquid with an acrid odor. Flash point 60°F. May polymerize exothermically if heated or contaminated. If the polymerization takes place inside a container, the container may rupture violently. Auto ignition temperature 721°F (383°C) (NTP). Less dense than water. Vapors heavier than air. Used to make paints and plastics.;Liquid;Liquid;COLOURLESS LIQUID WITH PUNGENT ODOUR.;Colourless mobile liquid; lachrymator/intense, harsh, fruity aroma;Colorless liquid with an acrid odor.;Colorless liquid with an acrid odor. Group: Polymers. CAS No. 9003-32-1. Pack Sizes: 1 kg. Product ID: ethyl prop-2-enoate. Molecular formula: 100.12g/mol. Mole weight: C5H8O2. CCOC(=O)C=C. InChI=1S/C5H8O2/c1-3-5(6)7-4-2/h3H, 1, 4H2, 2H3. JIGUQPWFLRLWPJ-UHFFFAOYSA-N. |  |
| Poly(ethyl acrylate) solution | average Mw ~95,000 by GPC, in toluene. Group: Hydrophobic polymers. |  |
| Poly(ethyl acrylate) solution | The polymer product is a hydrophobic material that is insoluble in water or other polar solvents. Uses: Biocompatible pea based copolymer membranes may find several s such as keratoprosthesis. Group: Hydrophobic polymers. Alternative Names: Acrylic acid ethyl ester polymer, Ethyl acrylate homopolymer. CAS No. 9003-32-1. Pack Sizes: 50 g in glass bottle. Product ID: ethyl prop-2-enoate. Molecular formula: average Mw ~95,000 by GPC. Mole weight: CH2CHCOOC2H5;C5H8O2;C5H8O2. CCOC(=O)C=C. 1S/C5H8O2/c1-3-5(6)7-4-2/h3H, 1, 4H2, 2H3. JIGUQPWFLRLWPJ-UHFFFAOYSA-N. | |
| Ethylene/ethyl acrylate copolymer,(0.78) | Ethylene/ethyl acrylate copolymer,(0.78). Uses: Designed for use in research and industrial production. Additional or Alternative Names: ETHYLENE/ETHYL ACRYLATE COPOLYMER;POLY(ETHYLENE-CO-ETHYL ACRYLATE);2-Propenoicacid,ethylester,polymerwithethene;poly(ethylene-ethylacrylate;POLY(ETHYLENE-CO-ETHYL ACRYLATE), MELT I NDEX 6;POLY(ETHYLENE-CO-ETHYL ACRYLATE), MELT I NDEX 20;Ethylene-ethyl acr. Product Category: Polymer/Macromolecule. Appearance: Beads. CAS No. 9010-86-0. Molecular formula: C21H36O6X2. Mole weight: 384.51. Density: 0.931. Product ID: ACM9010860. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Methoxy Poly(ethylene glycol) acrylate | Methoxy Poly(ethylene glycol) acrylate. CAS No. Product ID: 7-00115. Molecular formula: MeO-PEG-[OCOCH=CH2]. Mole weight: Mw 1,000. Purity: >98%. Properties: difunctional block copolymer with EO termini. Reference: Biochim. Biophys. Acta, 1062, 77, 1991; Biochim. Biophys. Acta, 1128, 44, 1992. Chem. Pharm. Bull., 39, 1620, 1991; Biochim. Biophys. Acta, 1149, 180, 1993. |  |
| Poly(2-ethylhexyl acrylate) | Poly(2-ethylhexyl acrylate). Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2-Propenoic acid, 2-ethylhexyl ester, homopolymer. Product Category: Biomaterials. CAS No. 9003-77-4. Molecular formula: (CH2CH[CO2CH2CH(C2H5)(CH2)3CH3])n. Product ID: ACM9003774. Alfa Chemistry ISO 9001:2015 Certified. | |
| Poly(2-ethylhexyl acrylate) solution | average Mw ~92,000 by GPC, in toluene. Group: Hydrophobic polymers. | |
| Poly(2-ethylhexyl acrylate) solution | Poly(2-ethylhexyl acrylate) solution can be prepared by polymerizing 2-ethylhexyl acrylate. It may also be synthesized by solution polymerization in toluene. Uses: Poly(2-ethylhexyl acrylate) solution may be used as plasticizer for medical grade pressure sensitive adhesives. Group: Hydrophobic polymers. Alternative Names: Poly(ethylhexyl acrylate), 2-Ethylhexyl acrylate homopolymer. CAS No. 9003-77-4. Pack Sizes: 50 g in glass bottle. Product ID: 2-ethylhexyl prop-2-enoate. Molecular formula: average Mw ~92,000 by GPC. Mole weight: (CH2CH[CO2CH2CH(C2H5)(CH2)3CH3])n. CCCCC(CC)OC(=O)C=C. 1S/C11H20O2/c1-4-7-8-10 (5-2)9-13-11 (12)6-3/h6, 10H, 3-5, 7-9H2, 1-2H3. GOXQRTZXKQZDDN-UHFFFAOYSA-N. | |
| Poly(9H-carbazole-9-ethyl acrylate) | Poly(9H-carbazole-9-ethyl acrylate). Group: other materials. Alternative Names: POLY(9H-CARBAZOLE-9-ETHYL ACRYLATE); poly[2-(9h-carbazol-9-yl)ethyl acrylate]. CAS No. 69678-49-5. Mole weight: (C17< / sub>H15< / sub>NO2< / sub>) n. 96%. | |
| Polyethyl acrylate | Polyethyl acrylate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2-Propenoicacid,ethylester,homopolymer;Ethyl2-propenoate,homopolymer;Ethylacrylate,homopolymer;Poly(acrylicacid,ethylester);POLY(ETHYL ACRYLATE);ETHYL ACRYLATE LATEX;ETHYL ACRYLATE RESIN;POLY(ETHYL ACRYLATE), SOLUTION IN TOLUEN E, AVERAGE MW CA. 95,000 (G. Product Category: Polymer/Macromolecule. CAS No. 9003-32-1. Mole weight: 100000. Density: 1.12. Product ID: ACM9003321. Alfa Chemistry ISO 9001:2015 Certified. | |
| Poly(ethyl acrylate/acrylic acid) | Poly(ethyl acrylate/acrylic acid). Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2-Propenoicacid,polymerwithethyl2-propenoate;Acrylicacid,ethylacrylatecopolymer;Ethyl2-propenoate,2-propenoicacid,polymer;Ethyl2-propenoate,2-propenoicacidpolymer;Ethylacrylate,acrylicacidcopolymer;Ethylacrylate,acrylicacidpolymer;POLY(ETHYL ACRYLATE/ACR. Product Category: Polymer/Macromolecule. CAS No. 25085-35-2. Product ID: ACM25085352. Alfa Chemistry ISO 9001:2015 Certified. | |
| Poly(ethylene-co-ethyl acrylate) | ethyl acrylate 18 wt. %, beads, melt index 20 g/10 min. Group: Hydrophobic polymers. | |
| 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) | 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 | Poly(ethylene glycol)behenyl ether methacrylate. Uses: Designed for use in research and industrial production. Additional or 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%. Product Category: Polymer/Macromolecule. CAS No. 125441-87-4. Molecular formula: H2C=C(CH3)CO2(CH2CH2O)n(CH2)21CH3. Product ID: ACM125441874. Alfa Chemistry ISO 9001:2015 Certified. | |
| 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)methyl ether acrylate | Poly(ethylene glycol)methyl ether acrylate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: ACRYL-PEG;METHOXYPOLY(ETHYLENE GLYCOL) ACRYLATE;METHOXYPOLYETHYLENE GLYCOL 5,000 ACRYLATE.alpha.-(1-Oxo-2-propenyl)-.omega.-methoxypoly(oxy-1,2-ethanediyl);2-ethanediyl). alpha.-(1-oxo-2-propenyl)-.omega.-methoxy-Poly(oxy-1;alpha-(1-oxo-2-propenyl)-omega. Product Category: Polymer/Macromolecule. CAS No. 32171-39-4. Molecular formula: H2C=CHCO2(CH2CH2O)nCH3. Product ID: ACM32171394. Alfa Chemistry ISO 9001:2015 Certified. | |
| 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. | |
| Poly(methacrylic acid-co-ethyl acrylate) Metharcylic acid copolymer dispersion | antidiabetic. Grades: USP/NF/JPE/EP. Product ID: 8-01283. | |
| Poly(methyl methacrylate) | Methyl methacrylate monomer appears as a clear colorless liquid. Slightly soluble in water and floats on water. Vapors heavier than air. Vapors irritate the eyes and respiratory system. Containers must be heavily insulated or shipped under refrigeration. An inhibitor such as hydroquinone, hydroquinone methyl ester and dimethyl t-butylphenol is added to keep the chemical from initiating polymerization. The chemical may polymerize exothermically if heated or contaminated with strong acid or base. If the polymerization takes place inside a container, the container may rupture violently. Used to make plastics. Uses: Acrylates and methacrylates are monomers that are combined with other monomers or polymers to produce plastics used in cosmetics, medicine, dentistry, and manufacturing industries.occupational asthma in operating room nurse; used to make lucite, plexiglas, paper coatings, latex paints, inks, polishes, dental restorations, adhesive cements, surgical implants, and impregnated concrete. Synonyms: METHYL METHACRYLATE POLYMER; METHYL METHACRYLATE, POLYMERIZED; METHYL METHACRYLATE RESIN; METHACRYLIC ACID METHYL ESTER POLYMER; LUCITE; POLY(METHYL METHACRYLATE-CO-ETHYL ACRYLATE); POLY(METHYL METHACRYLATE), ISOTACTIC; POLY(METHYL METHACRYLATE). Grades: 98%. CAS No. 9011-14-7. Molecular formula: (C5H8O2)x. Mole weight: 99.1083. |  |
| Poly(methyl methacrylate) | Poly(methyl methacrylate). Group: Polymers. Alternative Names: ETHYL ACRYLATE-METHYL METHACRYLATE LATEX; METHYL METHACRYLATE POLYMER; METHYL METHACRYLATE, POLYMERIZED; METHYL METHACRYLATE RESIN; METHACRYLIC ACID METHYL ESTER POLYMER; LUCITE; POLYBEAD(R) PMMA MICROSPHERES; POLYBEAD(R) POLY(METHYL METHACRYLATE) MICROSPHERES. CAS No. 9010-88-2. Product ID: ethyl prop-2-enoate; methyl 2-methylprop-2-enoate. Molecular formula: 200.23g/mol. Mole weight: C10H16O4. CCOC(=O)C=C.CC(=C)C(=O)OC. InChI=1S/2C5H8O2/c1-4(2)5(6)7-3; 1-3-5(6)7-4-2/h1H2, 2-3H3; 3H, 1, 4H2, 2H3. XPNLOZNCOBKRNJ-UHFFFAOYSA-N. | |
| Poly[(methyl methacrylate)-co-(9-H-carbazole-9-ethyl acrylate)] | Poly[(methyl methacrylate)-co-(9-H-carbazole-9-ethyl acrylate)]. Group: other materials. | |
| Poly(methyl methacrylate-co-ethyl acrylate) | Poly(methyl methacrylate-co-ethyl acrylate). Uses: Poly(methyl methacrylate-co-ethyl acrylate) (pmmaea) copolymers may be used to prepare single phase mixture with phenolic derivative. pmmaea may be used to form latex interpenetrating polymer networks (lipns). membranes of pmmaea were reportedly used for separation of heavy metal ions from aqueous solutions. Group: Bioelectronic materials hydrophobic polymersself assembly and lithography. CAS No. 9010-88-2. Pack Sizes: 1 kg in poly bottle. Product ID: ethyl prop-2-enoate; methyl 2-methylprop-2-enoate. Molecular formula: 200.23g/mol. Mole weight: [CH2C(CH3)(CO2CH3)]X[CH2CH(CO2C2H5]Y. CCOC(=O)C=C.CC(=C)C(=O)OC. 1S/2C5H8O2/c1-4(2)5(6)7-3; 1-3-5(6)7-4-2/h1H2, 2-3H3; 3H, 1, 4H2, 2H3. XPNLOZNCOBKRNJ-UHFFFAOYSA-N. | |
| Poly(methyl methacrylate),mw 25000(i.v. 0.18) | Poly(methyl methacrylate),mw 25000(i.v. 0.18). Uses: Designed for use in research and industrial production. Additional or Alternative Names: METHYL METHACRYLATE POLYMER;METHYL METHACRYLATE, POLYMERIZED;METHYL METHACRYLATE RESIN;METHACRYLIC ACID METHYL ESTER POLYMER;LUCITE;POLY(METHYL METHACRYLATE-CO-ETHYL ACRYLATE);POLY(METHYL METHACRYLATE), ISOTACTIC;POLY(METHYL METHACRYLATE). Product Category: Polymer/Macromolecule. Appearance: atactic pellets. CAS No. 9011-14-7. Molecular formula: [-CH2C(CH3)(CO2CH3)-]n. Mole weight: 25000. Density: 1.2. Product ID: ACM9011147. Alfa Chemistry ISO 9001:2015 Certified. | |
| 1,1,2,3,4,5-Hexaphenyl-1H-silole | HPS is an aggregation-induced emission (AIE) material for use in the OLED emitting layer. Photolysis and thermolysis of 1,4,5,6,7,7-hexaphenyl-7-silabicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic anhydride (XIb) may lead to the formation of hexaphenylsilacyclopentadiene. Uses: Hexaphenylsilacyclopentadiene may undergo π4s+π2s cycloaddition with ethyl acrylate to form bicyclosilaheptene. the same study reports similar cycloaddition reactions with various dienophiles. the reaction of hexaphenylsilacyclopentadiene with perbenzoic acid yields a mixture of tetraphenylfuran and cis-dibenzoylstilbene. Group: Organic light-emitting diode (oled) materials. Alternative Names: 1, 1, 2, 3, 4, 5-Hexaphenylsilacyclopenta-2, 4-diene, 1, 1, 2, 3, 4, 5-Hexaphenylsilacyclopentadiene, 1, 1, 2, 3, 4, 5-Hexaphenylsilole, HPS. CAS No. 752-28-3. Pack Sizes: 1 g in poly bottle. Product ID: 1,1,2,3,4,5-hexakis-phenylsilole. Molecular formula: 538.75. Mole weight: C40H30Si. C1 (C2=CC=CC=C2)=C (C3=CC=CC=C3)C (C4=CC=CC=C4)=C (C5=CC=CC=C5)[Si]1 (C6=CC=CC=C6)C7=CC=CC=C7. 1S/C40H30Si/c1-7-19-31 (20-8-1)37-38 (32-21-9-2-10-22-32)40 (34-25-13-4-14-26-34)41 (35-27-15-5-16-28-35, 36-29-17-6-18-30-36)39 (37)33-23-11-3-12-24-33/h1-30H, QAKMXYFDVPDIPT-UHFFFAOYSA-N. QAKMXYFDVPDIPT-UHFFFAOYSA-N. | |
| 2-(Dimethylamino)ethyl Acrylate | This compound was used as a reagent for investigating the hydrolytic stability of poly((2-?dimethylamino)?ethyl methacrylate) and comparing with the stability of its monomer. The result has been ascribed to a coordination of the protonated dimethylamino group and the ester carbonyl, rendering the ester more susceptible to nucleophilic attack of a hydroxyl ion. Group: Biochemicals. Grades: Highly Purified. CAS No. 2439-35-2. Pack Sizes: 5g, 25g. Molecular Formula: C7H13NO2, Molecular Weight: 143.18. US Biological Life Sciences. |  Worldwide |
| 2-Propenoic acid,2-methyl-,polymer with 1,1-dimethylethyl 2-propenoate and ethyl 2-propenoate | 2-Propenoic acid,2-methyl-,polymer with 1,1-dimethylethyl 2-propenoate and ethyl 2-propenoate. Group: Hydrophobic polymers. Alternative Names: 2-Propenoic acid, 2-methyl-, polymer with 1,1-dimethylethyl 2-propenoate and ethyl 2-propenoate; Copolymer aus tert.-Butylacrylat, Methacrylsure und Ethylacrylat; Poly(tert-butyl acrylate-co-ethyl acrylate-co-Methacrylic acid) powder, Methacrylic acid 23. CAS No. 159666-35-0. | |
| 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. | |
| 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. | |
| 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. | |
| 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. | |
| Acrylates Copolymer | Acrylates Copolymer is a type of polymer that is commonly used in many cosmetic products. It is a water-soluble polymer made up of several different monomers, including methyl methacrylate and butyl acrylate. Acrylates copolymer is added to cosmetic products to help them thicken, stabilize, and provide a smooth texture. Some of the cosmetic products that may contain acrylates copolymer include hairsprays, nail polishes, and lotions. In hairsprays, acrylates copolymer is used to help hold hair in place and provide a firm yet flexible hold. In nail polishes, acrylates copolymer is used to thicken the polish and help it adhere to the nail better. In lotions, acrylates copolymer is used to stabilize the emulsion, which allows the ingredients in the lotion to remain blended together. Uses: 1. acrylates copolymer is commonly used as a thickening agent in personal care products such as lotions, creams, and gels. 2. it is also used in hair care products such as hair sprays, mousses, and styling gels to provide hold and volume to the hair. 3. acrylates copolymer is used in sunscreen formulations to enhance the product's water resistance. 4. it is used in adhesives and sealants as a bind. Group: Polymers. Alternative Names: Polymer of one or more monomers of acrylic acid, methacrylic acid or one of their simple esters. CAS No. 25133-97-5. Product ID: ethyl prop-2-enoate; methyl 2-methylprop-2-enoate; 2-methylprop-2-enoic acid. | |
| 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. | |
| Perfluoroalkylethyl acrylate | Perfluoroalkylethyl acrylate. Group: Polymers. Alternative Names: Poly(difluoromethylene), α-fluoro-ω-[2- [(1-oxo-2-propenyl)oxy]ethyl]-; Perfluoroalkylethyl acrylate; Perfluoroalkyl Ethyl Acrylates; Poly(difluoroMethylene),a-fluoro-w-[2-[(1-oxo-2-propen-1-yl)oxy]ethyl]-; PFAEA (Perfluoroalkylethylacrylate). CAS No. 65605-70-1. Product ID: 3,3,3-trifluoropropyl prop-2-enoate. Molecular formula: 168.11g/mol. Mole weight: C6H7F3O2. C=CC(=O)OCCC(F)(F)F. InChI=1S/C6H7F3O2/c1-2-5 (10)11-4-3-6 (7, 8)9/h2H, 1, 3-4H2. NWBWGFFZPIVONT-UHFFFAOYSA-N. | |
| Poly(ethylene-co-acrylic acid),zinc salt | Poly(ethylene-co-acrylic acid),zinc salt. Uses: Designed for use in research and industrial production. Additional or Alternative Names: POLY(ETHYLENE-CO-ACRYLIC ACID), ZINC SALT;2-Propenoicacid,polymerwithethene,zincsalt;ETHYLENE/ZINC ACRYLATE COPOLYMER;POLY(ETHYLENE-CO-ACRYLIC ACIDZINC SAL;POLY(ETHYLENE-CO-ACRYLIC ACID), ZINC SAL T, 10 WT. % ACRYLIC ACID;Poly(ethylene-co-acrylic acid) zi. Product Category: Biomaterials. CAS No. 28208-80-2. Product ID: ACM28208802. Alfa Chemistry ISO 9001:2015 Certified. | |
| Sodium Polystyrene Sulfonate | Sodium Polystyrene Sulfonate. Synonyms: Poly(sodium-p-styrenesulfonate); PSS. CAS No. 25704-18-1. Product ID: PE-0437. Category: Coagulant; dispersant. Product Keywords: Pharmaceutical Excipients; Excipients for Liquid Dosage Form; Sodium Polystyrene Sulfonate; Dispersion Excipients; Coagulant; dispersant; 25704-18-1; 25704-18-1. UNII: 1699G8679Z. Grade: Pharmceutical Excipients. Administration route: Eye; Oral. Dosage Form: Suspension (including sustained-release formulations), sustained-release capsules and sustained-release tablets. Stability and Storage Conditions: Store in a well-sealed container. Commonly used amount and the maximum amount: Maximum oral dosage: 300mg; Dental external use and oral use: 20mg/g. Source and Preparation: This product is a copolymer of ethyl acrylate and methyl methacrylate and trimethyl ammonium methacrylate chloride. This product is divided into type A and type B by copolymer composition. When the drying product of the two types of copolymer is quantified, the copolymer composition is respectively trimethyl ammonium chloride (C9H18ClNO 2:207.70) 8.85 - 11.96% and 4.48 - 6.77%. |  |
| 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. | |
| 3-Glycidoxypropyltrimethoxysilane | It is epoxy functional silane used as adhesion promoters in SPUR, urethane, epoxy, polysulfide, silicone, and acrylic caulks, coatings, sealants and adhesives. Uses: It can improve the dry and wet strength of cured composites reinforced by glass fiber rovings, enhance the wet electrical properties of epoxy resin-based encapsulation and packaging materials, without the need to use separate primers in polysulfide and polyurethane sealants, and improve water-based acrylic adhesion of sealant, polyurethane and epoxy coatings. Group: Polymers. Alternative Names: Tetraethyl Orthosilicate ?Ethyl Silicate); Etylukrzemian(Polish); Silane, Tetraethoxy-; Silane,Tetraethoxy-; Silbond Condensed; Silester; Silicate D'Ethyle; Silicate Tetraethylique. CAS No. 2530-83-8. Pack Sizes: Packed with 5 L, 20 L or 210 L plastic/steel drum, 1000 L IBC container, or according to customer's requirement. Product ID: 3-Glycidoxypropyltrimethoxysilane. Molecular formula: 236.34. Mole weight: C9H20O5Si. 98%. | |
| 8arm-PEG10K-Acrylate | Hexaglycerol core, average Mn 10000. Group: Poly(ethylene glycol) and poly(ethylene oxide). | |
| 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. | |
| 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 | tripentaerythritol core, average Mn 20,000. Group: Poly(ethylene glycol) and poly(ethylene oxide). | |
| 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 | average Mn 2,000. Group: Poly(ethylene glycol) and poly(ethylene oxide). | |
| Acrylate-PEG3500-Acrylate | average Mn 3,500. Group: Poly(ethylene glycol) and poly(ethylene oxide). | |
| Acrylate-PEG3500-NHS | average Mn 3,500. Group: Poly(ethylene glycol) and poly(ethylene oxide). | |
| Acrylate-PEG5K-NHS | average Mn 5,000. Group: Poly(ethylene glycol) and poly(ethylene oxide). | |
| Acrylate-PEG7500-NHS | average Mn 7,500. Group: Poly(ethylene glycol) and poly(ethylene oxide). | |
| 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). | |
| 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%+. | |
| 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. | |
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