Alfa Chemistry Materials 5 - Products
Alfa Chemistry Materials is specialized in material chemistry and offers an extensive catalog of materials in a wide range of applications, including Metals and Materials, 3D Printing Materials, Biomaterials.
| Product | Description | |
|---|---|---|
| Poly(ethylene glycol) (N-hydroxysuccinimide 5-pentanoate) ether 2-(biotinylamino)ethane | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and redu. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: Biotin-PEG, Poly(ethylene glycol) (N-hydroxysuccinimide acetic acid) ether biotin, protected valeric acid, biotin carboxylic acid PEG, NHS - protected acid PEG, Biotin polyoxyethylene maleimide, Biotin-PEG maleimide, Biotinylated PEG. Pack Sizes: Packaging 100 mg in glass insert. Molecular formula: PEG ave |  |
| Poly(ethylene glycol) (N-hydroxysuccinimide 5-pentanoate) ether N'-(3-maleimidopropionyl)aminoethane | Poly(ethylene glycol) (N-hydroxysuccinimide 5-pentanoate) ether N'-(3-maleimidopropionyl)aminoethane. Group: Poly(ethylene glycol) and poly(ethylene oxide). CAS No. 851040-94-3. | |
| 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(ethylene glycol-ran-propylene glycol) | The polymer product is a hydrophobic material that is insoluble in water or other polar solvents. Uses: Hydraulic fluids, metal working fluids and lubricants, heat transfer fluids, solder assist fluids, quenchants, lubricants, solvents, plasticizers and foam control agents. Group: Hydrophobic polymerspeg-ppg copolymerspoly(ethylene glycol) and poly(ethylene oxide). Pack Sizes: 250 mL in glass bottle. Molecular formula: Mn ~2,500. OCCO.CC(O)CO. | |
| Poly(ethylene glycol-ran-propylene glycol) monobutyl ether | The polymer product is a hydrophobic material that is insoluble in water or other polar solvents. Uses: Hydraulic fluids, metal working fluids and lubricants, heat transfer fluids, solder assist fluids, quenchants, lubricants, solvents, plasticizers and foam control agents. Group: Hydrophobic polymerspeg-ppg copolymerspoly(ethylene glycol) and poly(ethylene oxide). CAS No. 9038-95-3. Pack Sizes: 1 L in poly bottle. Product ID: butan-1-ol; ethane-1,2-diol; propane-1,2-diol. Molecular formula: average Mn ~3,900. Mole weight: CH3(CH2)3(OCH2CH2)x[OCH2CH(CH3)]yOH. OCCO.CCCCO.CC(O)CO. 1S/C4H10O.C3H8O2.C2H6O2/c1-2-3-4-5; 1-3(5)2-4; 3-1-2-4/h5H, 2-4H2, 1H3; 3-5H, 2H2, 1H3; 3-4H, 1-2H2. QMNOIORHZMRPLS-UHFFFAOYSA-N. | |
| Polyethylene glycol solution | Polyethylene glycol solution. Group: Poly(ethylene glycol) and poly(ethylene oxide). CAS No. 25322-68-3. | |
| Poly(ethylene glycol) tetrahydrofurfuryl ether | 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: Mixture of diethylene and triethylene glycol mono-tetrahydrofurfuryl ether, Tetrahydrofurfuryl polyethylene glycol 200. CAS No. 31692-85-0. Product ID: 2-(oxolan-2-ylmethoxy)ethanol. Molecular formula: average Mn 200. Mole weight: C7H14O3. C1CC(OC1)COCCO. 1S / C7H14O3 / c8-3-5-9-6-7-2-1-4-10-7 / h7-8H, 1-6H2. CTPDSKVQLSDPLC-UHFFFAOYSA-N. | |
| Polyethylene-graft-maleic anhydride | Polyethylene is resistant to various organic solvents and corrosion of various acids and bases, but not to oxidative acids such as nitric acid. Polyethylene will oxidize in an oxidizing environment. Uses: Bond aid for polar to nonpolar substances. compatibilizer for polymer blends. Group: Hydrophobic polymers. Alternative Names: maleic copolymer, maleated copolymer, maleated polymer. CAS No. 9006-26-2. Pack Sizes: 250 g in poly bottle. 1S/C4H2O3.C2H4/c5-3-1-2-4(6)7-3; 1-2/h1-2H; 1-2H2. YYXLGGIKSIZHSF-UHFFFAOYSA-N. | |
| Poly(ethyleneimine) solution | All polyethylene imine polymers are hydrophilic and may contain approx. 30% hydrated water. Uses: Detergents, adhesives, water treatment, printing inks, dyes, cosmetics, and paper industry, adhesion promoter, lamination primer, fixative agent, flocculant, cationic dispersant, stability enhancer, surface activator, chelating agent, scavenger for aldehydes and oxides. protein precipitant. Group: Hydrophilic polymers. Alternative Names: Ethyleneimine polymer solution, PEI. CAS No. 9002-98-6. Pack Sizes: Packaging 1 g in glass bottle. Product ID: aziridine. Molecular formula: Mr 600,000-1,000,000. Mole weight: C2H5N;CH2NHCH2;C2H5N. C1CN1. 1S/C2H5N/c1-2-3-1/h3H,1-2H2. NOWKCMXCCJGMRR-UHFFFAOYSA-N. | |
| Poly(ethyleneimine) solution | Poly(ethyleneimine) solution. Group: Hydrophilic polymers. CAS No. 25987-06-8. | |
| Poly(ethylene oxide) | Poly(ethylene oxide). Group: Poly(ethylene glycol) and poly(ethylene oxide)polymers. CAS No. 25322-68-3. | |
| Poly(ethylene oxide), 4-arm, amine terminated | 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. | |
| Poly(ethylene oxide), 4-arm, carboxylic acid terminated | 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. | |
| Poly(ethylene oxide), 4-arm, hydroxy terminated | 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. | |
| Poly(ethylene oxide), 4-arm, succinimidyl succinate terminated | 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. | |
| Poly(ethylene oxide), 4-arm, thiol terminated | 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. | |
| Poly(ethylene oxide), 6-arm, hydroxy terminated | 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 17000. | |
| Poly(ethylene oxide)-block-polycaprolactone, 4-arm | Poly(ethylene oxide)-block-polycaprolactone, 4-arm. Group: Biodegradable polymerspoly(ethylene glycol) and poly(ethylene oxide). CAS No. 30174-06-2. | |
| Poly(ethylene oxide)-block-polylactide, 4-arm | We offer you this block copolymer with good biocompatibility. Group: Biodegradable polymerspoly(ethylene glycol) and poly(ethylene oxide). Pack Sizes: 250 mg in glass insert 1 g in glass bottle. Molecular formula: PLA average Mn ~3,500 poly(ethylene oxide) Mn ~2,500. | |
| Poly(ethylene succinate) | 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 polymerspolymers. Alternative Names: Ethylene glycol succinate. CAS No. 25569-53-3. Product ID: butanedioic acid; ethane-1,2-diol. Molecular formula: average Mw 10,000. Mole weight: (OCH2CH2O2CCH2CH2CO)n. OCCO.OC(=O)CCC(O)=O. 1S/C4H6O4.C2H6O2/c5-3(6)1-2-4(7)8; 3-1-2-4/h1-2H2, (H, 5, 6)(H, 7, 8); 3-4H, 1-2H2. VJVOPINBJQWMNY-UHFFFAOYSA-N. | |
| Polyethylenimine, 80% ethoxylated solution | The hydrophilic polymer contains polar or charged functional groups, making it soluble in water. Uses: Additive to coatings and printing inks, brightener in electroplating, cationic modifier in clays and starches and adhesion/substantivity promoter. Group: Hydrophilic polymers. Alternative Names: PEI. CAS No. 26658-46-8. Pack Sizes: Packaging 100, 250 g in poly bottle. Molecular formula: Mw 110,000. | |
| Polyethylenimine, branched | Ethyleneimine, stabilized appears as a clear colorless liquid with an ammonia-like odor. Flash point 12°F. Less dense than water. Flammable over a wide range of vapor-air concentrations. Vapors irritate the skin, eyes, nose, and throat. May be toxic by prolonged inhalation, skin absorption, or ingestion. Carcinogenic. Vapors heavier than air. May polymerize exothermically if heated or contaminated. If the polymerization takes place inside a container, the container may rupture violently.;COLOURLESS LIQUID WITH PUNGENT ODOUR.;Colorless liquid with an ammonia-like odor.;Colorless liquid with an ammonia-like odor. [Note: Usually contains inhibitors to prevent polymerization.]. Group: Hydrophilic polymerspolymers. CAS No. 9002-98-6. Product ID: aziridine. Molecular formula: 43.07g/mol. Mole weight: C2H5N;CH2NHCH2;C2H5N. C1CN1. InChI=1S/C2H5N/c1-2-3-1/h3H,1-2H2. NOWKCMXCCJGMRR-UHFFFAOYSA-N. | |
| Polyethylenimine, branched | All polyethylene imine polymers are hydrophilic and may contain approx. 30% hydrated water. Uses: Detergents, adhesives, water treatment, printing inks, dyes, cosmetics, and paper industry, adhesion promoter, lamination primer, fixative agent, flocculant, cationic dispersant, stability enhancer, surface activator, chelating agent, scavenger for aldehydes and oxides. Group: Hydrophilic polymers. Alternative Names: PEI, ethylenediamine branched. CAS No. 25987-06-8. Pack Sizes: Packaging 1 L in glass bottle 100, 250 mL in glass bottle. Molecular formula: average Mn ~600 by GPC average Mw ~800 by LS. Mole weight: H(NHCH2CH2)nNH2. 1S/C2H8N2.C2H5N/c3-1-2-4; 1-2-3-1/h1-4H2; 3H, 1-2H2. SFLOAOINZSFFAE-UHFFFAOYSA-N. | |
| Polyethylenimine hydrochloride | All polyethylene imine polymers are hydrophilic and may contain approx. 30% hydrated water. Uses: Polyethylenimine is a powerful, trustworthy, and cost-effective reagent that is widely regarded as the current gold standard for transfection in vitro and in vivo. it has a high density of protonatable amino groups with one amino nitrogen for every three atoms. Group: Hydrophilic polymers. Alternative Names: Linear PEI HCl salt, Poly(ethylene imine) HCl salt, Poly(ethylene imine hydrochloride). Molecular formula: average Mn 4,000. Mole weight: CH3(NHC2H4)nOH·xHCl. | |
| Polyethylenimine, linear | Ethyleneimine, stabilized appears as a clear colorless liquid with an ammonia-like odor. Flash point 12°F. Less dense than water. Flammable over a wide range of vapor-air concentrations. Vapors irritate the skin, eyes, nose, and throat. May be toxic by prolonged inhalation, skin absorption, or ingestion. Carcinogenic. Vapors heavier than air. May polymerize exothermically if heated or contaminated. If the polymerization takes place inside a container, the container may rupture violently.;COLOURLESS LIQUID WITH PUNGENT ODOUR.;Colorless liquid with an ammonia-like odor.;Colorless liquid with an ammonia-like odor. [Note: Usually contains inhibitors to prevent polymerization.]. Group: Hydrophilic polymers. CAS No. 9002-98-6. Product ID: aziridine. Molecular formula: 43.07g/mol. Mole weight: C2H5N;CH2NHCH2;C2H5N. C1CN1. InChI=1S/C2H5N/c1-2-3-1/h3H,1-2H2. NOWKCMXCCJGMRR-UHFFFAOYSA-N. | |
| Poly(ethyl vinyl ether) | 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. Alternative Names: Ethyl vinyl ether homopolymer, Vinyl ethyl ether polymer. CAS No. 25104-37-4. Product ID: ethenoxyethane. Molecular formula: average Mw ~3,800 by GPC. Mole weight: [-CH2CH(OC2H5)-]n. CCOC=C. 1S/C4H8O/c1-3-5-4-2/h3H,1,4H2,2H3. FJKIXWOMBXYWOQ-UHFFFAOYSA-N. | |
| Poly-γ-benzyl-L-glutamate | Poly-γ-benzyl-L-glutamate. Group: Polyamino acids. CAS No. 25014-27-1. Product ID: 2-amino-5-oxo-5-phenylmethoxypentanoic acid. Molecular formula: 237.25g/mol. Mole weight: C12H15NO4. C1=CC=C(C=C1)COC(=O)CCC(C(=O)O)N. InChI=1S/C12H15NO4/c13-10 (12 (15)16)6-7-11 (14)17-8-9-4-2-1-3-5-9/h1-5, 10H, 6-8, 13H2, (H, 15, 16). BGGHCRNCRWQABU-UHFFFAOYSA-N. | |
| Poly(γ-ethyl-L-glutamate) | Poly(γ-ethyl-L-glutamate). Group: Polyamino acids. CAS No. 25189-52-0. | |
| Poly(Glu, Ala, Tyr) sodium salt | Poly(Glu, Ala, Tyr) sodium salt. Group: Polyamino acids. CAS No. 97105-01-6. | |
| Poly(Glu, Lys) hydrobromide | Poly(Glu, Lys) hydrobromide. Group: Polyamino acids. CAS No. 119039-90-6. | |
| Poly(Glu, Lys, Tyr) sodium salt | Poly(Glu, Lys, Tyr) sodium salt. Group: Polyamino acids. CAS No. 118539-64-3. | |
| Poly(Glu, Tyr)-Agarose | Poly(Glu, Tyr)-Agarose. Group: Polyamino acids. | |
| Polyglycolide-block-poly(ethylene glycol)-block-polyglycolide | Polyglycolide-block-poly(ethylene glycol)-block-polyglycolide. Group: Biodegradable polymers. | |
| Poly(hexadecyl methacrylate) solution | Poly(hexadecyl methacrylate) belongs to a class of long chain of poly (alkyl) methacrylate. It can be dissolved in benzene and heptane. Group: Bioelectronic materials hydrophobic polymersself assembly and lithography. Alternative Names: Cetyl methacrylate homopolymer,Hexadecyl methacrylate homopolymer,Palmityl methacrylate homopolymer,Poly(cetyl methacrylate). CAS No. 25986-80-5. Pack Sizes: 25 g in glass bottle. Mole weight: (C20H38O2)n. CCCCCCCCCCCCCCCCOC(=O)C(C)=C. | |
| Poly(hexyl methacrylate) solution | Poly(hexadecyl methacrylate) belongs to a class of long chain of poly (alkyl) methacrylate. It can be dissolved in benzene and heptane. Uses: Poly(hexyl methacrylate)(phma) may be used to prepare amphiphilic block copolymers with -poly(ethylene oxide) (peo). these block copolymers may be used as structure directing agents for the preparation organic-inorganic hybrid materials from organic, volatile solvents. Group: Bioelectronic materials hydrophobic polymersself assembly and lithography. Alternative Names: Hexyl methacrylate homopolymer,Poly(1-hexyl methacrylate). CAS No. 25087-17-6. Pack Sizes: 25 g in glass bottle. Mole weight: (C10H18O2)n. CCCCCCOC(=O)C(C)=C. | |
| Polyisobutylene | Polyisobutylene. Group: Hydrophobic polymersorganic field effect transistor (ofet) materials. Alternative Names: 2-methyl-1-propenhomopolymer. CAS No. 9003-27-4. Pack Sizes: 100, 250 g in poly bottle. Molecular formula: 56.10. Mole weight: [CH2C(CH3)2]n. CC(C)=C. 1S/C4H8/c1-4(2)3/h1H2, 2-3H3, VQTUBCCKSQIDNK-UHFFFAOYSA-N. VQTUBCCKSQIDNK-UHFFFAOYSA-N. | |
| Poly[(isobutylene-alt-maleic acid, ammonium salt)-co-(isobutylene-alt-maleic anhydride)] | Poly[(isobutylene-alt-maleic acid, ammonium salt)-co-(isobutylene-alt-maleic anhydride)] (PIM) is a water soluble polymer. Uses: Pim may be used to prepare montmorillonite (mmt) clay and amylopectin-based nanocomposites. pim may be used as a dispersant for the preparation of nio/y3o3-zro2 for solid oxide fuel cells (sofcs). pim may also find use as a coupling agent.binder for ceramic powders and dispersing agent for water soluble paints. binder for ceramic powders and dispersing agent for water soluble paints. Group: Hydrophobic polymers. Alternative Names: maleic copolymer, maleated copolymer, maleated polymer. CAS No. 55893-87-3. Pack Sizes: 250 g in glass bottle. Molecular formula: average Mw ~60,000. Mole weight: (C4H2O3 · C4H8)m · xH3N. | |
| Poly(isobutyl methacrylate) | Poly(isobutyl methacrylate). Group: Bioelectronic materials hydrophobic polymersself assembly and lithography. CAS No. 9011-15-8. | |
| Polylactide-block-poly(ethylene glycol)-block-polylactide | We offer you this block copolymer with good biocompatibility. Group: Biodegradable polymerspoly(ethylene glycol) and poly(ethylene oxide). Alternative Names: PLA-PEG-PLA. Pack Sizes: 1 g in glass bottle. Molecular formula: PEG average Mn 10,000 PLA average Mn 1,000 average Mn (1,000-10,000-1,000). Mole weight: HO(CHCH3COO)x(CH2CH2O)y(COCHCH3O)zH. | |
| Poly(lactide-co-caprolactone)-block-poly(ethylene glycol)-block-poly(lactide-co-caprolactone) | It belongs to the family of synthetic biodegradable polymers. PLCL-PEG-PLCL polymers are studies extensively for its drug delivery capability (both hydrophobic and hydrophilic drugs). Uses: 1. drug delivery 2. ligament-bone interface mimicking. Group: Biodegradable polymerspoly(ethylene glycol) and poly(ethylene oxide). Alternative Names: PLCL-PEG-PLCL. Pack Sizes: 1 g in glass bottle. Molecular formula: PEG average Mn 5,000 (DCM, PEO) PLCL average Mn 5,700 average Mn (1,000-10,000-1,000). | |
| Poly[(lactide-co-ethylene glycol)-co-ethyloxyphosphate] | The polymer is structurally similar to nucleic and teichoic acids. It undergoes biodegrade through hydrolysis and possibly enzymatic digestion. One of the few classes of polymers for non-viral gene delivery by conjugation of charged groups to the side chain of the phosphate.This biodegradable polymer is soluble in a variety of organic acids. Group: Biodegradable polymers. Alternative Names: Poly(LAEG-EOP). Pack Sizes: 1 g in glass bottle. Mole weight: [OCCH3CO (OCHCH3CO)xOCH2CH2O (COCHCH3O)yCOCHCH3OPOOCH2CH3]n. | |
| Poly(lactide-co-glycolide)-block-poly(ethylene glycol)-block-poly(lactide-co-glycolide) | PLGA-PEG-PLGA is an amphiphilic triblock copolymer which can self-assemble into micelles in aqueous medium due to the hydrophobic interactions present in the hydrophobic segments. The PEG segment imparts hydrophilicity and improves the biocompatibility of the copolymer. The PLGA segment forms a hydrophobic core and can solubilize hydrophobic drugs. These copolymers are widely used as nanocarriers for the sustained release of drugs. Uses: Used in the synthesis of targeted nanoparticles which are used for differential delivery and controlled release of drugs. Group: Biodegradable polymerspoly(ethylene glycol) and poly(ethylene oxide). Alternative Names: PLGA-PEG-PLGA. Pack Sizes: 1 g in glass bottle. Molecular formula: PEG average Mn 1,000 PLGA average Mn 2,200 average Mn (1100-1000-1100). | |
| Poly-L-histidine | Solid;White crystals or crystalline powder; odourless. Group: Polyamino acids. CAS No. 26062-48-6. Product ID: (2S)-2-amino-3-(1H-imidazol-5-yl)propanoic acid. Molecular formula: 155.15g/mol. Mole weight: C6H9N3O2;C6H9N3O2. C1=C(NC=N1)CC(C(=O)O)N. InChI=1S/C6H9N3O2/c7-5 (6 (10)11)1-4-2-8-3-9-4/h2-3, 5H, 1, 7H2, (H, 8, 9) (H, 10, 11)/t5-/m0/s1. HNDVDQJCIGZPNO-YFKPBYRVSA-N. | |
| Poly-L-histidine hydrochloride | Poly-L-histidine hydrochloride. Group: Polyamino acids. CAS No. 61857-39-4. | |
| Poly(L-lactide) | Liquid;Liquid;colourless liquid. Group: Biodegradable polymerspolyamino acids. CAS No. 26161-42-2. Product ID: methyl 2-methylpropanoate. Molecular formula: 102.13g/mol. Mole weight: C5H10O2. CC(C)C(=O)OC. InChI=1S/C5H10O2/c1-4(2)5(6)7-3/h4H, 1-3H3. BHIWKHZACMWKOJ-UHFFFAOYSA-N. | |
| Poly(L-lactide), 2-bromoisobutyryl terminated | Poly(L-lactide) (PLLA) and its copolymers are among the most studied biodegradable polymers. PLLA is a crystalline polymer with good mechanical properties. The applications of PLLA are mainly concentrated in biomedical applications. Uses: Macroinitiator for atom transfer radical polymerization (atrp) to prepare block copolymers. poly(l-lactide) is commonly used in drug delivery. Group: Biodegradable polymers. Alternative Names: ATRP terminated PLLA, PLA, ATRP Macromonomer. Pack Sizes: 1 g in glass bottle. Molecular formula: average Mn 5,500. Mole weight: H(C3H4O2)nC6H10BrO3. | |
| Poly(L-lactide) 4-cyano-4-[ (dodecylsulfanylthiocarbonyl) sulfanyl]pentonate | Poly(L-lactide) (PLLA) and its copolymers are among the most studied biodegradable polymers. PLLA is a crystalline polymer with good mechanical properties. The applications of PLLA are mainly concentrated in biomedical applications. Uses: The poly(l-lactide) is a biodegradable polymer that contains raft agent functionality. the benzodithioate moiety is well suited to polymerize methacrylates and methacrylamides. pla is commonly used in several applications, including drug delivery, nanoparticle surface modification, end-group functionalization, macroinitiator or block precursor. Group: Biodegradable polymers. Alternative Names: PLA thiocarbonyl, PLA RAFT, PLLA RAFT. Pack Sizes: 1 g in glass bottle. Molecular formula: average Mn 18,000. Mole weight: C19H35NOS3(C3H4O2)n. | |
| Poly(L-lactide-block-acrylic acid) | The PLLA-block-PAA is a biocompatible diblock copolymer which forms cylindrical micelles. The PLLA is hydrophobic and a degradable block, and the PAA is hydrophilic. Uses: The diblock polymer can be used to form nanoparticles and micelles or scaffolds. Group: Biodegradable polymers. Alternative Names: PLLA-PAA, PLLA-b-PAA. Pack Sizes: 1 g in glass bottle. Molecular formula: PAA Mn 18,000 PLLA Mn 4,500. Mole weight: C13H25S3(C3H4O2)yC6H9NO(C3H4O2)xH. | |
| Poly(L-lactide)-block-poly(ethylene glycol)methyl ether | Poly(L-lactide) (PLLA) and its copolymers are among the most studied biodegradable polymers. PLLA is a crystalline polymer with good mechanical properties. The applications of PLLA are mainly concentrated in biomedical applications. Group: Biodegradable polymerspoly(ethylene glycol) and poly(ethylene oxide). Alternative Names: Poly(ethylene glycol)-block-poly(lactone) methyl ether, Poly(ethylene glycol)methyl ether-block-polylactide. Pack Sizes: 250 mg in glass insert 1 g in glass bottle. Molecular formula: PEG average Mn ~5,000 PLLA average Mn ~5,000. | |
| Poly(L-lactide-co-5-methyl-5-allyloxycarbonyl-1,3-dioxan- 2-one) | This product we offer is a degradable polymer. Uses: This biodegradable random copolymer has pendant alkene functional groups along the back bone and a hydroxyl end-group. the pendant functionality along the chain enables bioconjugation of growth factors via thiol-ene click chemistry. the monomer ratio for mac:l-lactide is 1:9. Group: Biodegradable polymers. Alternative Names: poly(L-lactide-co-MAC), polycarbonate copolymer, PLA-co-MAC, PLLA-co-MAC. Pack Sizes: 1 g in glass bottle. Molecular formula: Mn 10,000. Mole weight: CH3(C3H4O2)n(C9H12O5)mH. | |
| Poly(L-lactide-co-caprolactone) | Poly(l-lactide-co-ε-caprolactone) (PLCL), the copolymer of L-lactic (LA) and ε-caprolactone (CL). Uses: Biodegradable and bioabsorbable polymers have attracted considerable attention because they mimic the mechanical properties of human soft tissue. poly(l-lactide-co-ε-caprolactone) (plcl) has found applications in many areas of tissue engineering and regenerative medicine. Group: Biodegradable polymers. Alternative Names: PLLA-PCL. Mole weight: CH3(C6H10O2)m(C6H8O4)nCH3. | |
| Poly(L-lactide-co-D,L-lactide) | Poly(L-lactide-co-D,L-lactide). Group: Biodegradable polymers. | |
| Poly(L-lactide-co-trimethylene carbonate) | Poly(L-lactide-co-trimethylene carbonate) (PLT) copolymers were synthesized by ring opening polymerization of L-lactide (LLA) and trimethylene carbonate (TMC). Uses: Cardiac occluder, in vitro degradable body, internal implantation. Group: Biodegradable polymers. Alternative Names: PLA-TMC. Mole weight: CH3[C6H8O4]m[C4H6O3]nCH3. | |
| Poly-L-lysine-FITC Labeled | Poly-L-lysine-FITC Labeled. Group: Polyamino acids. | |
| Poly-L-lysine hydrobromide | Poly-L-lysine hydrobromide. Group: Polyamino acids. Alternative Names: L-Lys-(L-Lys)n-L-Lys.xHBr. CAS No. 25988-63-0. Product ID: (2S) -6-amino-2- [ [ (2S) -6-amino-2- [ [ (2S) -2, 6-diaminohexanoyl] amino] hexanoyl] amino] hexanoic acid. Molecular formula: 402.5g/mol. Mole weight: C18H38N6O4. C (CCN)CC (C (=O)NC (CCCCN)C (=O)NC (CCCCN)C (=O)O)N. InChI=1S/C18H38N6O4/c19-10-4-1-7-13 (22)16 (25)23-14 (8-2-5-11-20)17 (26)24-15 (18 (27)28)9-3-6-12-21/h13-15H, 1-12, 19-22H2, (H, 23, 25) (H, 24, 26) (H, 27, 28)/t13-, 14-, 15-/m0/s1. WBSCNDJQPKSPII-KKUMJFAQSA-N. | |
| Poly-L-lysine solution | Poly-L-lysine solution. Group: Polyamino acids. CAS No. 25988-63-0. Product ID: (2S) -6-amino-2- [ [ (2S) -6-amino-2- [ [ (2S) -2, 6-diaminohexanoyl] amino] hexanoyl] amino] hexanoic acid. Molecular formula: 402.5g/mol. Mole weight: C18H38N6O4. C (CCN)CC (C (=O)NC (CCCCN)C (=O)NC (CCCCN)C (=O)O)N. InChI=1S/C18H38N6O4/c19-10-4-1-7-13 (22)16 (25)23-14 (8-2-5-11-20)17 (26)24-15 (18 (27)28)9-3-6-12-21/h13-15H, 1-12, 19-22H2, (H, 23, 25) (H, 24, 26) (H, 27, 28)/t13-, 14-, 15-/m0/s1. WBSCNDJQPKSPII-KKUMJFAQSA-N. | |
| Poly-L-lysine, succinylated | Poly-L-lysine, succinylated. Group: Polyamino acids. | |
| Poly-L-ornithine hydrochloride | White crystalline solid or powder to syrup; Slight savoury aroma. Group: Polyamino acids. CAS No. 26982-21-8. Product ID: (2S)-2,5-diaminopentanoic acid; hydrochloride. Molecular formula: 168.62g/mol. Mole weight: C5H13ClN2O2. C(CC(C(=O)O)N)CN.Cl. InChI=1S/C5H12N2O2. ClH/c6-3-1-2-4(7)5(8)9; /h4H, 1-3, 6-7H2, (H, 8, 9); 1H/t4-; /m0. /s1. GGTYBZJRPHEQDG-WCCKRBBISA-N. | |
| Poly-L-ornithine solution | Poly-L-ornithine solution. Group: Polyamino acids. CAS No. 27378-49-0. Product ID: 2,5-diaminopentanoic acid; hydrobromide. Molecular formula: 213.07g/mol. Mole weight: C5H13BrN2O2. C(CC(C(=O)O)N)CN.Br. InChI=1S/C5H12N2O2. BrH/c6-3-1-2-4(7)5(8)9; /h4H, 1-3, 6-7H2, (H, 8, 9); 1H. GWRQMKDBBHFVIZ-UHFFFAOYSA-N. | |
| Poly-L-threonine | Poly-L-threonine. Group: Polyamino acids. CAS No. 82822-12-6. Product ID: 2-[5-(4-methylphenyl)tetrazol-2-yl]acetic acid. Molecular formula: 218.21g/mol. Mole weight: C10H10N4O2. CC1=CC=C(C=C1)C2=NN(N=N2)CC(=O)O. InChI=1S/C10H10N4O2/c1-7-2-4-8 (5-3-7)10-11-13-14 (12-10)6-9 (15)16/h2-5H, 6H2, 1H3, (H, 15, 16). QBJSWVLDHWIJDK-UHFFFAOYSA-N. | |
| Poly(Lys, Phe) 1:1 hydrobromide | Poly(Lys, Phe) 1:1 hydrobromide. Group: Polyamino acids. CAS No. 26700-39-0. | |
| Poly(maleic anhydride-alt-1-octadecene) | The polymer product is a hydrophobic material that is insoluble in water or other polar solvents. Uses: Release coatings, anti-corrosive, thickening agent, chelant/surfactant and cross-linker for epoxy or alcohol functional polymers. Group: Hydrophobic polymers. Alternative Names: maleic copolymer, maleated copolymer, maleated polymer. Pack Sizes: 1 kg in poly bottle. | |
| Poly(methacrylic acid, sodium salt) solution | The hydrophilic polymer contains polar or charged functional groups, making it soluble in water. Uses: Water treatment agent for cooling towers, boilers and heat exchangers. Group: Hydrophilic polymers. Alternative Names: Sodium polymethacrylate, Sodium polymethacrylic acid, Poly(methacrylic acid) sodium salt. CAS No. 54193-36-1. Pack Sizes: Packaging 1 L in poly bottle. Product ID: sodium; 2-methylprop-2-enoate. Molecular formula: average Mn ~5,400 average Mw ~9,500 by GPC. Mole weight: [CH2C(CH3)(CO2Na)]n. CC(=C)C(=O)O[Na]. 1S/C4H6O2.Na/c1-3(2)4(5)6;/h1H2, 2H3, (H, 5, 6);/q;+1/p-1. SONHXMAHPHADTF-UHFFFAOYSA-M. | |
| Poly(methyl acrylate), azide terminated | Poly(methyl acrylate), azide terminated. Group: Hydrophobic polymers. | |
| Poly(methyl acrylate) solution | The polymer product is a hydrophobic material that is insoluble in water or other polar solvents. Uses: Pma/methylamine borane (meab) composites, prepared by solution blending process finds uses as a hydrogen storage material with better dehydrogenation property compared to meab. Group: Hydrophobic polymers. Alternative Names: Methyl acrylate homopolymer, Acrylic acid methyl ester polymer. CAS No. 9003-21-8. Pack Sizes: 50, 100 g in glass bottle. Molecular formula: average Mw ~40,000 by GPC. Mole weight: (C4H6O2)n. COC(=O)C=C. | |
| Poly(methylhydrosiloxane), trimethylsilyl terminated | Poly(methylhydrosiloxane), trimethylsilyl terminated. Group: Bioelectronic materials self assembly and lithography. Alternative Names: Methyl hydrogen polysiloxane. CAS No. 63148-57-2. Pack Sizes: 20 mL in poly bottle. Molecular formula: Mn ~390. Mole weight: (CH3)3SiO[SiH(CH3)O]nSi(CH3)3. [H][Si](C)(C)O. C[Si](C)(C)C. C[Si](C)(C)O. | |
| 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-co-ethylene glycol dimethacrylate) | Particles of this polymer can be prepared by dispersion polymerization. Uses: Light diffusing agent in plastics, matting agent, anti-blocking agent and pore-forming agent in ceramics. Group: Bioelectronic materials hydrophobic polymersself assembly and lithography. CAS No. 25777-71-3. Pack Sizes: 500 g in glass bottle. Product ID: methyl 2-methylprop-2-enoate; 2-(2-methylprop-2-enoyloxy)ethyl 2-methylprop-2-enoate. Molecular formula: 298.33g/mol. Mole weight: [-CH2C (CH3) (CO2CH3)-]X[CH2 (C-) (CH3)CO2CH2CH2O2C (C-) (CH3)CH2-]Y. COC(=O)C(C)=C. CC(=C)C(=O)OCCOC(=O)C(C)=C. 1S/C10H14O4. C5H8O2/c1-7 (2)9 (11)13-5-6-14-10 (12)8 (3)4; 1-4 (2)5 (6)7-3/h1, 3, 5-6H2, 2, 4H3; 1H2, 2-3H3. XBDAKYZJVVYINU-UHFFFAOYSA-N. | |
| Poly(methyl methacrylate-co-methacrylic acid) | 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: Bioelectronic materials hydrophobic polymersself assembly and lithography. Alternative Names: Poly(methacrylic acid-co-methyl methacrylate). CAS No. 25086-15-1. Pack Sizes: 1 kg in poly bottle. Product ID: methyl 2-methylprop-2-enoate; 2-methylprop-2-enoic acid. Molecular formula: average Mn ~15,000 by GPC average Mw ~34,000 by GPC. Mole weight: C9H14O4. CC(=C)C(=O)O.CC(=C)C(=O)OC. 1S/C5H8O2.C4H6O2/c1-4(2)5(6)7-3; 1-3(2)4(5)6/h1H2, 2-3H3; 1H2, 2H3, (H, 5, 6). IWVKTOUOPHGZRX-UHFFFAOYSA-N. | |
| Poly(methyl methacrylate), isotactic | i-PMMA can be prepared from t-C4H9MgBr. Structure of crystalline isotactic poly(methyl methacrylate) (i-PMMA) was investigated by X-ray diffraction and infra red spectroscopic techniques. Uses: The polymeric blend of isotatic (i-) poly-(methyl methacrylate) & 6,13-bis(triisopropylsilylethynyl) pentacene can be used to prepare thin films transistors (tfts). Group: Bioelectronic materials hydrophobic polymersself assembly and lithography. Alternative Names: Isotactic PMMA,Isotactic methyl methacrylate polymer,Isotactic poly(methyl methacrylate). CAS No. 25188-98-1. Pack Sizes: 1 g in glass bottle. Product ID: diethoxyphosphoryl (2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-(2-methoxy-2-oxoethoxy)iminoacetate. Molecular formula: 395.33g/mol. Mole weight: (C5H8O2)n. CCOP (=O) (OCC)OC (=O)C (=NOCC (=O)OC)C1=CSC (=N1)N. InChI=1S/C12H18N3O8PS/c1-4-21-24 (18, 22-5-2)23-11 (17)10 (8-7-25-12 (13)14-8)15-20-6-9 (16)19-3/h7H, 4-6H2, 1-3H3, (H2, 13, 14)/b15-10-. DOXUHDDTLHKPOE-GDNBJRDFSA-N. | |
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