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The hydrophilic polymer contains polar or charged functional groups, making it soluble in water. Uses: Pnipam-based smart surfaces for cell sheet tissue engineering intelligent swelling/collapsing copolymer that can be used as a temperature- and ph-sensitive materials. Group: Heterocyclic organic compound. Alternative Names: functionalized polyNIPAM, functionalized polyacrylamide, Polyacrylamide, Poly(NIPAM-co-MAA), polyNIPAM. CAS No. 151954-97-1. Molecular formula: (C6H11NO)m (C4H6O2)n. Mole weight: average Mn 50,000. Purity: 0.96. IUPACName: 2-methylprop-2-enoic acid;N-propan-2-ylprop-2-enamide. Canonical SMILES: CC(C)NC(=O)C=C.CC(=C)C(=O)O. Catalog: ACM151954971-1.
Intelligent Swelling/Collapsing copolymer that can be used as a temperature- and pH-sensitive material. Uses: Pnipam-based smart surfaces for cell sheet tissue engineering. Group: Hydrophilic polymers. Alternative Names: Poly(NIPAM-co-MAA-co-ODA), functionalized polyNIPAM, functionalized polyacrylamide, Polyacrylamide, polyNIPAM. Pack Sizes: Packaging 5 g in glass bottle. Molecular formula: Mn 30,000-60,000. Mole weight: (C6H11NO)m (C4H6O2)n (C21H40O2)p.
The hydrophilic polymer contains polar or charged functional groups, making it soluble in water. Uses: This copolymer is 90 mol% n-isopropylacrylamide, 10 mol% nhs activated ester. the nhs ester allows conjugation to a variety of functional groups. the end group functionality contains a carboxylic acid on one end. Group: Hydrophilic polymers. Alternative Names: PNIPAM. Pack Sizes: Packaging 1 g in glass bottle. Molecular formula: average Mn 5,000. Mole weight: C4H7O2[C6H11NO]x[C8H9NO3]yC13H25S3.
Poly(N-isopropylacrylamide), maleimide terminated
The hydrophilic polymer contains polar or charged functional groups, making it soluble in water. Uses: Pnipam-based smart surfaces for cell sheet tissue engineering novel polymer for development of thermosensitive coated micro/nano materials including thermoresponsive polymeric drug delivery systems. the maleimide functional group can be used to conjugate a variety of biomolecules such as enzymes and dna to the polymer chain. Group: Hydrophilic polymerspolymers. Alternative Names: P(NIPAM)n-NH-maleimide, functionalized polyNIPAM, functionalized polyacrylamide, Polyacrylamide, polyNIPAM. Pack Sizes: Packaging 1, 5 g in glass bottle. Molecular formula: average Mn 2,000. Mole weight: (C6H11NO)n SCH2CH2NH(CO)CH2CH2CH2(C4H2NO2).
The hydrophilic polymer contains polar or charged functional groups, making it soluble in water. Uses: Pnipam-based smart surfaces for cell sheet tissue engineering novel polymer for development of thermosensitive coated micro/nano materialincluding thermoresponsive polymeric drug delivery systems. the nhs ester functional group can be used to conjugate a variety of biomolecules such as enzymes to the polymer chain. Group: Hydrophilic polymers. Alternative Names: functionalized polyNIPAM, functionalized polyacrylamide, Polyacrylamide, NIPAM polymer, PNIPAM-NHS, polyNIPAM. Pack Sizes: Packaging 1, 5 g in glass bottle. Molecular formula: average Mn 2,000. Mole weight: (C6H11NO)n SCH2CH2COO(C4H4NO2).
The hydrophilic polymer contains polar or charged functional groups, making it soluble in water. Uses: This polymer is thermosensitive and can be coated on glass, silica, iron oxide, or other oxide nanoparticles, larger particles, or other surfaces. pnipam based polymers are typically used in biomedical s such as in cell sheet culture and tissue engineering. Group: Hydrophilic polymers. Alternative Names: PNIPAM. Pack Sizes: Packaging 1, 5 g in poly bottle. Molecular formula: average Mn 10000.
Poly[nitrilo (diphenoxyphosphoranylidyne)]
Poly[nitrilo (diphenoxyphosphoranylidyne)]. Group: other materials. Alternative Names: SP 100 (phosphazene); Phenoxyphosphazene Oligomer. CAS No. 28212-48-8. Mole weight: (C12H10NPO2)n. 99%.
Poly[n,N-(1,3-phenylene)isophthalamide]
Poly[n,N-(1,3-phenylene)isophthalamide]. Group: Hydrophobic polymers. Alternative Names: POLY[N,N-(1,3-PHENYLENE)ISOPHTHALAMIDE]; 1, 3-Benzenedicarbonyldichloride, polymerwith1, 3-benzenediamine. CAS No. 25765-47-3. Mole weight: (C14< / sub>H14< / sub>N2< / sub>O2< / sub>) n.
Poly(N,N-(1,3-phenylene)isophthalamide)
Poly(N,N-(1,3-phenylene)isophthalamide) can be used in heat and flame protective clothing. Synonyms: 1,3-Benzenediamine-1,3-benzenedicarbonyl dichloride copolymer; 1,3-Benzenediamine-isophthalyl chloride copolymer; m-Diaminobenzene-isophthaloyl chloride copolymer; m-Phenylenediamine-isophthaloyl chloride copolymer. CAS No. 25765-47-3. Molecular formula: C14H12Cl2N2O2. Mole weight: 311.2.
Poly[(N,N'-bis(4-butylphenyl)-N,N'-diphenyl-1,4-benzenediamine)-alt-(9,9-dioctylfluorene-2,7-diyl)], Mw 10,000-100,000 by GPC
Poly[(N,N'-bis(4-butylphenyl)-N,N'-diphenyl-1,4-benzenediamine)-alt-(9,9-dioctylfluorene-2,7-diyl)], Mw 10,000-100,000 by GPC. Group: Organic solar cell (opv) materials. CAS No. 223569-28-6.
Heterocyclic Organic Compound. Alternative Names: POLY(N,N-DIMETHYL-3,5-DIMETHYLENE PIPERIDINIUM CHLORIDE). CAS No. 113277-70-6. Density: 1.033. Catalog: ACM113277706.
Poly(N,N-Dimethylacrylamide)
Poly(N,N-Dimethylacrylamide). Group: Polymers.
Poly(N, N-dimethylacrylamide), DDMAT terminated
Poly(N, N-dimethylacrylamide), DDMAT terminated. Group: other plastics.
Poly(N,N-dimethylacrylamide), DDMAT terminated
Need help choosing the correct RAFT Agent? Please consult the RAFT Agent to Monomer compatibility table. Uses: Poly(n; n-dimethylacrylamide) is generally used in biological s. additionally; the alpha-chain end is a functional carboxylic acid (for potential specialty/coupling reactions). ddmat is especially suited for the polymerization of styrene; acrylate; and acrylamide monomers to make lithographically and biologically important block copolymers. useful as a chain transfer agent (cta) or a functionalized polymer. Group: Hydrophilic polymers. Alternative Names: polydimethylacrylamide methylpropionic acid dodecyltrithiocarbonate, PDMAM, polyDMAM. Pack Sizes: Packaging 1 g in glass bottle. Molecular formula: average Mn 10,000. Mole weight: HOCOCH (CH3)2 (CH2CHCON (CH3)2)nSCS2C12H25.
polynucleotide 3'-phosphatase
Also hydrolyses nucleoside 2'-, 3'- and 5'-monophosphates, but only 2'- and 3'-phosphopolynucleotides. Group: Enzymes. Synonyms: 2'(3')-polynucleotidase; DNA 3'-phosphatase; deoxyribonucleate 3'-phosphatase; 5'-polynucleotidekinase 3'-phosphatase. Enzyme Commission Number: EC 3.1.3.32. CAS No. 37288-16-7. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3635; polynucleotide 3'-phosphatase; EC 3.1.3.32; 37288-16-7; 2'(3')-polynucleotidase; DNA 3'-phosphatase; deoxyribonucleate 3'-phosphatase; 5'-polynucleotidekinase 3'-phosphatase. Cat No: EXWM-3635.
polynucleotide 5'-hydroxyl-kinase
Also acts on 5'-dephospho-RNA 3'-mononucleotides. Group: Enzymes. Synonyms: ATP:5'-dephosphopolynucleotide 5'-phosphatase; PNK; polynucleotide 5'-hydroxyl kinase (phosphorylating); 5'-hydroxyl polynucleotide kinase; 5'-hydroxyl polyribonucleotide kinase; 5'-hydroxyl RNA kinase; DNA 5'-hydroxyl kinase; DNA kinase; polynucleotide kinase; polynucleotide 5'-hydroxy-kinase. Enzyme Commission Number: EC 2.7.1.78. CAS No. 37211-65-7. PNK. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3107; polynucleotide 5'-hydroxyl-kinase; EC 2.7.1.78; 37211-65-7; ATP:5'-dephosphopolynucleotide 5'-phosphatase; PNK; polynucleotide 5'-hydroxyl kinase (phosphorylating); 5'-hydroxyl polynucleotide kinase; 5'-hydroxyl polyribonucleotide kinase; 5'-hydroxyl RNA kinase; DNA 5'-hydroxyl kinase; DNA kinase; polynucleotide kinase; polynucleotide 5'-hydroxy-kinase. Cat No: EXWM-3107.
polynucleotide 5'-phosphatase
Does not act on nucleoside monophosphates. Induced in Escherichia coli by T-even phages. Group: Enzymes. Synonyms: 5'-polynucleotidase. Enzyme Commission Number: EC 3.1.3.33. CAS No. 37288-17-8. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3636; polynucleotide 5'-phosphatase; EC 3.1.3.33; 37288-17-8; 5'-polynucleotidase. Cat No: EXWM-3636.
polynucleotide adenylyltransferase
Also acts slowly with CTP. Catalyses template-independent extension of the 3'- end of a DNA strand by one nucleotide at a time. Cannot initiate a chain de novo. The primer, depending on the source of the enzyme, may be an RNA or DNA fragment, or oligo(A) bearing a 3'-OH terminal group. See also EC 2.7.7.6 DNA-directed RNA polymerase. Group: Enzymes. Synonyms: NTP polymerase; RNA adenylating enzyme; AMP polynucleotidylexotransferase; ATP-polynucleotide adenylyltransferase; ATP:polynucleotidylexotransferase; poly(A) polymerase; poly(A) synthetase; polyadenylate nucleotidyltransferase; polyadenylate polym. Enzyme Commission Number: EC 2.7.7.19. CAS No. 9026-30-6. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3233; polynucleotide adenylyltransferase; EC 2.7.7.19; 9026-30-6; NTP polymerase; RNA adenylating enzyme; AMP polynucleotidylexotransferase; ATP-polynucleotide adenylyltransferase; ATP:polynucleotidylexotransferase; poly(A) polymerase; poly(A) synthetase; polyadenylate nucleotidyltransferase; polyadenylate polymerase; polyadenylate synthetase; polyadenylic acid polymerase; polyadenylic polymerase; terminal riboadenylate transferase; poly(A) hydrolase; RNA formation factors, PF1; adenosine triphosphate:ribonucleic acid adenylyltransferase. Cat No: EXWM-3233.
Polynucleotide Phosphorylase from Escherichia coli, Recombinant
Polynucleotide phosphorylase (PNPase) is a bifunctional enzyme with a phosphorolytic 3' to 5' exoribonuclease activity and a 3'-terminal oligonucleotide polymerase activity. It is also involved in mRNA processing and degradation in bacteria, plants, and humans. Applications: Polynucleotide phosphorylase (pnp) has been used in a study to show that spontaneous mutations resulting from replication errors are reduced in a pnp-deficient strain. it has also been used in a study to show that the absence of pnpase makes e. coli cells sensitive to uv, which suggests pnp has a role in survival of uv damage. Group: Enzymes. Synonyms: PNPase; nucleoside diphosphate:polynucleotidyl transferase; polyribonucleotide nucleotidyltransferase; polynucleotide phosphorylase; polyribonucleotide phosphorylase; EC 2.7.7.8; 9014-12-4. Enzyme Commission Number: EC 2.7.7.8. CAS No. 9014-12-4. Polynucleotide phosphorylase. Storage: -70°C. Form: Supplied as a solution in 20 mM Hepes buffer pH 7.9, 0.1 mM EDTA, 2 mM DTT, 12.5 mM MgCl2, 200 mM KCl, 21.4% (w/v) Glycerol. Source: E. coli. Species: Escherichia coli. PNPase; nucleoside diphosphate:polynucleotidyl transferase; polyribonucleotide nucleotidyltransferase; polynucleotide phosphorylase; polyribonucleotide phosphorylase; EC 2.7.7.8; 9014-12-4. Cat No: NATE-0608.
Polynucleotide phosphorylase from Human, Recombinant
Polynucleotide phosphorylase (PNPase) is a bifunctional enzyme with a phosphorolytic 3' to 5' exoribonuclease activity and a 3'-terminal oligonucleotide polymerase activity. It is also involved in mRNA processing and degradation in bacteria, plants, and humans. Group: Enzymes. Synonyms: PNPase; nucleoside diphosphate:polynucleotidyl transferase; polyribonucleotide nucleotidyltransferase; polynucleotide phosphorylase; polyribonucleotide phosphorylase; EC 2.7.7.8; 9014-12-4. Enzyme Commission Number: EC 2.7.7.8. CAS No. 9014-12-4. Polynucleotide phosphorylase. Storage: -70°C. Form: supplied as a solution in 20 mM HEPES buffer, pH 7.9, with 0.1 mM EDTA, 2 mM DTT, 12.5 mM MgCl2, ~130 mM KCl, and 20% (w/v) glycerol. Source: E. coli. Species: Human. PNPase; nucleoside diphosphate:polynucleotidyl transferase; polyribonucleotide nucleotidyltransferase; polynucleotide phosphorylase; polyribonucleotide phosphorylase; EC 2.7.7.8; 9014-12-4. Cat No: NATE-0609.
Polynucleotide phosphorylase from Synechocystis sp., Recombinant
Polynucleotide phosphorylase (PNPase) is a bifunctional enzyme with a phosphorolytic 3' to 5' exoribonuclease activity and a 3'-terminal oligonucleotide polymerase activity. It is also involved in mRNA processing and degradation in bacteria, plants, and humans. Polynuclotide phosphorlyase in spinach chloroplasts acts as a exonuclease and a poly (a) polymerase. Applications: Polynucleotide phosphorylase has been used in a study to discover that a major function of pnpase is the synthesis of cdp. it has also been used in a study to investigate the enzyme responsible for rna 3?-tail synthesis in s. coelicolor. Group: Enzymes. Synonyms: PNPase; nucleoside diphosphate:polynucleotidyl transferase; polyribonucleotide nucleotidyltransferase; polynucleotide phosphorylase; polyribonucleotide phosphorylase; EC 2.7.7.8; 9014-12-4. Enzyme Commission Number: EC 2.7.7.8. CAS No. 9014-12-4. Polynucleotide phosphorylase. Storage: -70°C. Source: E. coli. Species: Synechocystis sp. PNPase; nucleoside diphosphate:polynucleotidyl transferase; polyribonucleotide nucleotidyltransferase; polynucleotide phosphorylase; polyribonucleotide phosphorylase; EC 2.7.7.8; 9014-12-4. Cat No: NATE-0610.
Biomaterials. Alternative Names: POLY[[OCTAHYDRO-5-(METHOXYCARBONYL)-5-METHYL-4,7-METHANO-1 H-INDENE-1,3-DIYL]-1,2-ETHANEDIYL];poly((octahydro-5-(methoxycarbonyl)-5-me-4,7-meth;POLY((OCTAHYDRO-5-(METHOXYCARBONYL)-5-ME -4,7-METHANO-1H-INDENEDIYL)-ETHANEDIYL). CAS No. 123322-60-1. Molecular formula: (C15H20O2)n. Catalog: ACM123322601.
Polyolefin Elastomer
Polyolefin elastomer is a key functional modifier for a variety of polyolefin systems. This material has lower density, lower modulus, and a lower melting point vs. polyethylene or polypropylene. Due to these traits, POE is often used as an impact or softness modifier. Additionally, POE can be used in flexible products such as film. It has the ability to modify heat seal initiation temperatures (HSIT) as well as promote "easy-peel" properties. Uses: Car bumpers | side doors | auto interior plastics | hosing and jacketing | food packaging | easy-peel plastics | biaxially oriented polypropylene (bopp) | shoe soles | shoe foam. Group: other plastics.
Polyolefin Polyol
Polyolefin Polyol. Group: Polymers.
Polyols
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Polyoxin A is a nucleoside antifungal antibiotic produced by Str. cacaor var. asoensis and Str. piomogenus. Synonyms: (S-(E))-1-(5-((2-Amino-5-O-(aminocarbonyl)-2-deoxy-L-xylonoyl)amino)-1,5-dideoxy-1-(3,4-dihydro-5-(hydroxymethyl)-2,4-dioxo-1(2H)-pyrimidinyl)-beta-D-allofuranuronoyl)-3-ethylidene-2-azetidinecarboxylic acid. Grades: 95%. CAS No. 19396-03-3. Molecular formula: C23H32N6O14. Mole weight: 616.53.
Polyoxin B
Polyoxin B is a nucleoside antifungal antibiotic produced by Str. cacaor var. asoensis and Str. piomogenus. Synonyms: Polyoxin AL; piomycin; (2S)-2-[[(2S,3S,4S)-2-amino-5-carbamoyloxy-3,4-dihydroxypentanoyl]amino]-2-[(2R,3S,4R,5R)-3,4-dihydroxy-5-[5-(hydroxymethyl)-2,4-dioxopyrimidin-1-yl]oxolan-2-yl]acetic acid. Grades: Assay 70%. CAS No. 19396-06-6. Molecular formula: C17H25N5O13. Mole weight: 507.41.
Polyoxin B
Polyoxin B is a fungicide used in the protection of crops and pesticides. Group: Biochemicals. Grades: Highly Purified. CAS No. 19396-06-6. Pack Sizes: 1mg, 5mg. Molecular Formula: C17H25N5O13, Molecular Weight: 507.41. US Biological Life Sciences.
Worldwide
Polyoxin C
Polyoxin C is a nucleoside antifungal antibiotic produced by Str. cacaor var. asoensis and Str. piomogenus. Synonyms: Julimycin C. Grades: >98%. CAS No. 21027-33-8. Molecular formula: C11H15N3O8. Mole weight: 317.25.
Polyoxin N
Polyoxin is a nucleoside antifungal antibiotic produced by Str. cacaor var. asoensis and Str. piomogenus. Synonyms: Allofuranuronic acid, 5-((2-amino-5-O-(aminocarbonyl)-2-deoxy-L-xylonamino)-1,5-dideoxy-1-(4-formyl-2,3-dihydro-2-oxo-1H-imidazol-1-yl)-, beta-D-. CAS No. 37362-29-1. Molecular formula: C16H23N5O12. Mole weight: 477.38.
Polyoxirane-2,3-dicarboxylic acid
Polyoxirane-2,3-dicarboxylic acid. Group: Polymers. CAS No. 51274-37-4.
Polyoxorim
Polyoxorim is a member of the class of polyoxins that is isolated from the soil organism Streptomyces cacaoi var. asoensis. Polyoxorim exhibits fungicidal properties and may be used on rice, industrial grounds, golf courses and parks. It has a role as an EC 2.4.1.16 (chitin synthase) inhibitor and an antifungal agrochemical. It is a polyoxin and an antibiotic fungicide. Synonyms: 5-[[2-Amino-5-O-(aminocarbonyl)-2-deoxy-L-xylonoyl]amino]-1-(5-carboxy-3,4-dihydro-2,4-dioxo-1(2H)-pyrimidinyl)-1,5-dideoxy-β-D-allofuranuronic acid; Polyoxin D; 1-{5-[{[2-amino-5- (carbamoyloxy)-3, 4-dihydroxypentanoyl]amino} (carboxy)methyl]-3, 4-dihydroxytetrahydrofuran-2-yl}-2, 4-dioxo-1, 2, 3, 4-tetrahydropyrimidine-5-carboxylic acid(non-preferred name); Polyoxin D, Streptomyces cacaoi var asoensis. Grades: ≥96%. CAS No. 22976-86-9. Molecular formula: C17H23N5O14. Mole weight: 521.39.
Poly(oxy-1,2-ethanediyl),a-hydro-w-hydroxy-, ether with methyl D-glucopyranoside (3:1),ether with a-[3-(dodecyldimethylammonio)-2-hydroxypropyl]-w-hydroxypoly(oxy-1,2-ethanediyl)chloride (1:1) (9CI)
Heterocyclic Organic Compound. Alternative Names: Poly(oxy-1,2-ethanediyl). alpha.-hydro-.omega.-hydroxy-, ether with methyl D-glucopyranoside (3:1), ether with. alpha. -3-(dodecyldimethylammonio)-2-hydroxypropyl-. omega. -hydroxypoly(oxy-1, 2-ethanediyl) chloride (1:1);lauryl gluceth-10 hydroxypropyl dimo. CAS No. 123005-57-2. Catalog: ACM123005572.
Poly(oxy-1,2-ethanediyl),.alpha.-(2-ethylhexyl)-.omega.-hydroxy-, phosphate, sodium salt
Heterocyclic Organic Compound. Alternative Names: Poly(oxy-1,2-ethanediyl). alpha.-(2-ethylhexyl)-.omega.-hydroxy-, phosphate, sodium salt. CAS No. 111798-26-6. Catalog: ACM111798266.
Poly(oxy-1,2-ethanediyl),a-sulfo-w-[1-[(4-nonylphenoxy)methyl]-2-(2-propen-1-yloxy)ethoxy]-,branched, ammonium salts. Group: other glass and ceramic materials. CAS No. 184719-88-8.
Poly(oxy-1,2-ethanediyl),a-undecyl-w-hydroxy-, branched and linear
Heterocyclic Organic Compound. CAS No. 127036-24-2. Catalog: ACM127036242.