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| Product | Description | |
|---|---|---|
| Aqueous cationic polymer | Heterocyclic Organic Compound. CAS No. 10882-76-0. Appearance: Liquid. Purity: 0.4. Catalog: ACM10882760-1. |  |
| 1,1'-Bis(dimethylsilyl)ferrocene | Catalytic co-initiator in free radical photopolymerization and free radical promoted cationic polymerization reactions Reactant for: Hydrosilylataion and hydroboration reactions Platinum/nickel catalyzed selective hydrosilylation of alkynes and alkenes Iron-catalyzed dehydrogenative coupling reactions Hydrosilylation and double silylation of carbonyl compounds. Group: Polymer/macromolecule. Alternative Names: 1,1-BIS(DIMETHYLSILYL)FERROCENE;1,1-Bis(dimethylsilyl)ferrocene 97%;Ferrocene,1,1-bis(dimethylsilyl)-. CAS No. 1295-15-4. Molecular formula: C14H22FeSi2 10*. Mole weight: 302.34. Catalog: ACM1295154. | |
| 1-Naphthyl diphenylsulfonium triflate | Cationic photoinitiator. Photoacid generator. Uses: This product is suitable for scientific research. Group: Polymer/macromolecule. Alternative Names: DIPHENYL(NAPHTHYL)SULFONIUM TRIFLATE; DIPHENYL(NAPHTHYL)SULPHONIUM TRIFLATE;1-NAPHTHYL DIPHENYLSULFONIUM TRIFLATE;2-NAPHTHYL DIPHENYLSULFONIUM TRIFLATE; 1-Naphthalenyldiphenylsulfonium trifluoromethanesulfonate; 2-Naphthyldiphenylsulfonium trifluoromethanesulf. CAS No. 116808-69-6. Molecular formula: C23H17F3O3S2. Mole weight: 450.49. Purity: 0.96. IUPACName: naphthalen-1-yl(diphenyl)sulfanium; trifluoromethanesulfonate. Canonical SMILES: [O-]S (=O) (=O)C (F) (F)F. c1ccc (cc1)[S+] (c2ccccc2)c3cccc4ccccc34. Density: 1.3g/cm³. Catalog: ACM116808696-1. | |
| (4-Fluorophenyl)diphenylsulfonium triflate | Cationic photoinitiator. Photoacid generator. Group: Polymer/macromolecule. Alternative Names: 4-Fluorophenyl diphenylsulfonium trifluoromethanesulfonate. CAS No. 154093-57-9. Molecular formula: C19H14F4O3S2. Mole weight: 430.4g/mol. IUPACName: (4-fluorophenyl)-diphenylsulfanium; trifluoromethanesulfonate. Canonical SMILES: [O-]S(=O)(=O)C(F)(F)F. Fc1ccc(cc1)[S+](c2ccccc2)c3ccccc3. Catalog: ACM154093579. | |
| (4-Iodophenyl)diphenylsulfonium triflate | Cationic photoinitiator. Photoacid generator. Group: Polymer/macromolecule. Alternative Names: (4-Iodophenyl)diphenylsulfonium trifluoromethanesulfonate. CAS No. 255056-46-3. Molecular formula: C19H14F3IO3S2. Mole weight: 538.3g/mol. IUPACName: (4-iodophenyl)-diphenylsulfanium; trifluoromethanesulfonate. Canonical SMILES: [O-]S(=O)(=O)C(F)(F)F. Ic1ccc(cc1)[S+](c2ccccc2)c3ccccc3. Catalog: ACM255056463. | |
| (4-Methoxyphenyl)diphenylsulfonium triflate | Cationic photoinitiator. Photoacid generator. Group: Polymer/macromolecule. Alternative Names: (4-Methoxyphenyl)diphenylsulfonium trifluoromethanesulfonate. CAS No. 116808-67-4. Molecular formula: C20H17F3O4S2. Mole weight: 442.5g/mol. IUPACName: (4-methoxyphenyl)-diphenylsulfanium; trifluoromethanesulfonate. Canonical SMILES: [O-]S(=O)(=O)C(F)(F)F. COc1ccc(cc1)[S+](c2ccccc2)c3ccccc3. Catalog: ACM116808674. | |
| (4-Phenylthiophenyl)diphenylsulfonium triflate | Cationic photoinitiator. Photoacid generator. Group: Polymer/macromolecule. Alternative Names: (4-Phenylthiophenyl)diphenylsulfonium trifluoromethanesulfonate. CAS No. 111281-12-0. Molecular formula: C25H19F3O3S3. Mole weight: 520.6g/mol. IUPACName: diphenyl-(4-phenylsulfanylphenyl)sulfanium; trifluoromethanesulfonate. Canonical SMILES: [O-]S (=O) (=O)C (F) (F)F. S (c1ccccc1)c2ccc (cc2)[S+] (c3ccccc3)c4ccccc4. Catalog: ACM111281120. | |
| (4-tert-Butylphenyl)diphenylsulfonium triflate | Cationic photoinitiator. Photoacid generator. Group: Polymer/macromolecule. Alternative Names: (4-tert-Butylphenyl)diphenylsulfonium trifluoromethanesulfonate. CAS No. 145612-66-4. Molecular formula: C23H23F3O3S2. Mole weight: 468.6g/mol. IUPACName: (4-tert-butylphenyl)-diphenylsulfanium; trifluoromethanesulfonate. Canonical SMILES: [O-]S (=O) (=O)C (F) (F)F. CC (C) (C)c1ccc (cc1)[S+] (c2ccccc2)c3ccccc3. Catalog: ACM145612664. | |
| Acrylate Copolymer | This polymer is a hydrophobic high molecular weight carboxylated acrylic copolymer. Because acrylate copolymer is anionic, compatibility must be evaluated when formulating with cationic ingredients. CAS No. 129702-02-9. Pack Sizes: 1 kg. Product ID: CDC10-0551. Category: Cosmetic Thickeners. Product Keywords: Cosmetic Ingredients; Cosmetic Thickeners; Acrylate Copolymer; CDC10-0551; 129702-02-9; 129702-02-9. Color: White. Physical State: Powder. Storage: Store in a closed container at a dry place at room temperature. |  |
| Acrylate Copolymer | This polymer is a hydrophobic high molecular weight carboxylated acrylic copolymer. Because acrylate copolymer is anionic, compatibility must be evaluated when formulating with cationic ingredients. Uses: Color cosmetics, sun & skin protection, hair care products, shaving creams, moisturizers. Group: Cationic surfactants & conditioning agents. CAS No. 129702-02-9. Appearance: Fine white powder. Catalog: CI-HC-0054. | |
| Acryloyl Chloride | Acryloyl chloride is an acid chloride that has the ability to undergo free radical polymerization and is used as an acylating agent for amino glass slides. Acryloyl chloride is also used as a binding agent in the preparation of cationic copolymer hydrogels. Group: Biochemicals. Grades: Highly Purified. CAS No. 814-68-6. Pack Sizes: 10g, 25g. Molecular Formula: C3H3ClO. US Biological Life Sciences. |  Worldwide |
| Allylamine dihydrogen phosphate | Polyallylamine hydrochloride is a cationic polyelectrolyte prepared by the polymerization of allylamine. Uses: Poly(allylamine hydrochloride) has many biomedical applications. the most prominent use of this polyelectrolyte is in the field of cell encapsulation. a layer by layer method is used by alternating positively and negatively charged polyelectrolytes to build a barrier between the cell and the harsher outside environment. upon cell lysis, the capsule of layered polyelectrolytes maintains its structural integrity and can be used for purposes such as drug delivery. Group: Heterocyclic organic compoundallyl monomers. Alternative Names: phosphoricacid; prop-2-en-1-amine. CAS No. 121092-93-1. Molecular formula: C3H10NO4P. Mole weight: 155.09 g/mol. Purity: 0.95. IUPACName: phosphoric acid;prop-2-en-1-amine. Canonical SMILES: NCC=C.OP(O)(O)=O. Catalog: ACM-MO-121092931. | |
| Benzyldodecyldimethylammonium bromide | Benzyldodecyldimethylammonium bromide. Uses: Benzalkonium bromides are an important class of cationic surfactants. they are used as preservatives for ophthalmic, nasal and parenteral products and they are also used as a topical antiseptic and medical equipment disinfectant. Group: Polymerization additives. Alternative Names: Benzyldimethyldodecylammonium bromide. CAS No. 7281-4-1. Pack Sizes: 1 kg. Product ID: benzyl-dodecyl-dimethylazanium; bromide. Molecular formula: 384.44. Mole weight: C21H38BrN. CCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1. [Br-]. InChI=1S/C21H38N. BrH/c1-4-5-6-7-8-9-10-11-12-16-19-22 (2, 3)20-21-17-14-13-15-18-21; /h13-15, 17-18H, 4-12, 16, 19-20H2, 1-3H3; 1H/q+1; /p-1. KHSLHYAUZSPBIU-UHFFFAOYSA-M. ≥96.5%. |  |
| Bis(4-tert-butylphenyl)iodonium triflate | Cationic photoinitiator. Photoacid generator. Group: Polymer/macromolecule. Alternative Names: DtBPIT, Bis(4-tert-butylphenyl)iodonium trifluoromethanesulfonate. CAS No. 84563-54-2. Molecular formula: [(CH3)3CC6H4]2ICF3SO3. Mole weight: 542.39. Purity: ≥ 97%. IUPACName: bis(4-tert-butylphenyl)iodanium; trifluoromethanesulfonate. Canonical SMILES: [O-]S (=O) (=O)C (F) (F)F. CC (C) (C)c1ccc ([I+]c2ccc (cc2)C (C) (C)C)cc1. Catalog: ACM84563542-2. | |
| Branched PEI-g-PEG | PEI-g-PEG is a graft copolymer of branched PEI (bPEI), which is modified with multiple PEGs of indicated MW. The PEG to PEI ratio is the average number of PEGs per PEI. Uses: Copolymers of cationic poly(ethyleneimine) wight grafted with polyethylene glycol (peg) (pei-g-peg) are extremely well-studied compounds that markedly improve the in vitro and in vivo delivery of oligonucleotides (aos) to cells and tissues. by varying the mw of pei, as well as the nature of peg shielding, peg-pei-ao nanoparticulates can be prepared with a dynamic range of size, surface charge, and stability. each of these properties in-turn influences the transfection capacity of the peg-pei-ao polyplexes. in addition, peg-pei copolymers are readily functionalized for enhanced efficacy and specificity of cellular and tissue targeting. Group: Hydrophilic polymers. Alternative Names: PEI-PEG, Branched polyethylenimine-graft-poly(ethylene glycol), PEI-g-PEG. Molecular formula: PEG Mn 550. Mole weight: H3CO[ (CH2)2O]nC12H23N3O3[NH (CH2)2]mNH2. | |
| Bromanilic Acid | A benzoquinone derivative that acts as an electron acceptor in cationic polymerization. Group: Biochemicals. Alternative Names: 2,5-Dibromo-3,6-dihydroxy-2,5-cyclohexadiene-1,4-dione; 2,5-Dibromo-3,6-dihydroxy-p-benzoquinone; 2,5-Dibromo-3,6-dihydroxyquinone; 2,5-Dihydroxy-3,6-dibromo-1,4-benzoquinone; NSC 36928. Grades: Highly Purified. CAS No. 4370-59-6. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Diallyldimethylammonium (chloride) (60% in water) | Diallyldimethylammonium chloride (60% in water) is a quaternary ammonium compound belonging to the class of alkylammonium salts. The compound is widely used as a cationic monomer in the production of water-soluble polymers, especially in the manufacture of flocculants and coagulants for water treatment processes. In addition, it can be used as an antimicrobial agent, surfactant or adhesive in various industrial applications. Its unique chemical properties make it an important ingredient in a variety of industrial processes, including papermaking, textiles and personal care products. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: N,N-Dimethyl-N-2-propenyl-2-propen-1-aminium chloride. CAS No. 7398-69-8. Pack Sizes: 25 g. Product ID: HY-W106486. |  |
| Diphenyliodonium hexafluorophosphate | Cationic photoinitiator. Photoacid generator. Group: Polymer/macromolecule. Alternative Names: DPIHFP. CAS No. 58109-40-3. Molecular formula: (C6H5)2I(PF6). Mole weight: 426.08. Purity: 0.96. IUPACName: di(phenyl)iodanium. Canonical SMILES: F[P-](F)(F)(F)(F)F. [I+](c1ccccc1)c2ccccc2. ECNumber: 261-134-5. Catalog: ACM58109403. | |
| Diphenyliodonium hexafluorophosphate | Diphenyliodonium hexafluorophosphate. Uses: Cationic photoinitiator. photoacid generator. Group: Self assembly and lithographyelectronic materials polymerization reagents. Alternative Names: DPIHFP. CAS No. 58109-40-3. Pack Sizes: 5, 25 g in amber poly bottle. Product ID: di(phenyl)iodanium. Molecular formula: 426.08. Mole weight: (C6H5)2I(PF6). F[P-](F)(F)(F)(F)F. [I+](c1ccccc1)c2ccccc2. 1S/C12H10I. F6P/c1-3-7-11 (8-4-1)13-12-9-5-2-6-10-12; 1-7 (2, 3, 4, 5)6/h1-10H; /q+1; -1. DSSRLRJACJENEU-UHFFFAOYSA-N. 96%. | |
| Diphenyliodonium p-toluenesulfonate | Cationic photoinitiator. Photoacid generator. Group: Polymer/macromolecule. Alternative Names: DPIpTS. CAS No. 6293-66-9. Molecular formula: (C6H5)2IC6H4(SO3)CH3. Mole weight: 452.3g/mol. IUPACName: diphenyliodanium;4-methylbenzenesulfonate. Canonical SMILES: Cc1ccc(cc1)S([O-])(=O)=O. [I+](c2ccccc2)c3ccccc3. Catalog: ACM6293669. | |
| Guar Gum, Cationic | Cationic guar gum is a modified, naturally derived (from the seeds of the guar plant cyampopis tetragonolobus) quaternary, high-molecular weight sugar polymer (polysaccharide) combining both thickening and conditioning effects. Uses: Shampoos, conditioners, lotions, creams, body washes, shower gels. Group: Cationic surfactants & conditioning agents. CAS No. 65497-29-2. Appearance: Yellowish powder, faint characteristic odor. Catalog: CI-HC-0061. | |
| Ime | Ime. Group: Polymers. Alternative Names: IME; POLY(ETHYLENE OXIDE), DIAMINE TERMINATED; 1H-Imidazole, polymerwith(chloromethyl)oxirane; Epichlorohydrin,imidazolepolymer; Imidazole,epichlorohydrinpolymer; reaction product of imidazole and epichlorohydrin; Cationicpolymerinwater; AQUEOUS CATIONIC POLYMER. CAS No. 68797-57-9. Product ID: 2-(chloromethyl)oxirane; 1H-imidazole. Molecular formula: 160.603. Mole weight: (C3< / sub>H5< / sub>ClO?C3< / sub>H4< / sub>N2< / sub>) x. C1C(O1)CCl.C1=CN=CN1. SDKQKTMVNUGBPR-UHFFFAOYSA-N. 96%. | |
| N,N-Dimethyl-N-2-Propenyl-2-Propen-1-Aminium Chloride Polymer With 2-Propenamide | Cationic Surfactants. Alternative Names: Dimethyldiallylammonium chloride acrylamide polymer;n,n-dimethyl-n-2-propenyl-2-propen-1-aminium chloride polymer with 2-propenamide;POLYQUATERNIUM-7. CAS No. 108464-53-5. Molecular formula: (C8H16ClN)n.(C3H5NO)m. Mole weight: 232.75. Catalog: ACM108464535. | |
| Poly(2-ethyl-2-oxazoline) | 2-Ethyl-2-oxazoline is an oxazoline which is used particularly as a monomer for the cationic ring-opening polymerization to poly(2-alkyloxazoline)s. This type of polymers are under investigation as readily water-soluble and biocompatible materials for biomedical applications. Uses: The polymerization of 2-ethyl-2-oxazoline can also be carried out as a living cationic polymerization. copolymers with other 2-alkyl-2-oxazolines and other monomers can prepare random and block copolymers. the obtained copolymers can be used as biocompatible drug carriers for coatings and adhesives, among many other applications. elimination of propionyl groups from poly(2-ethyl-2-oxazoline) yields linear polyethyleneimine. Group: Hydrophilic polymers. Alternative Names: Me-PEtOx-OH. Product ID: 2-ethyl-4,5-dihydro-1,3-oxazole. Molecular formula: average Mn 5,000. Mole weight: CH3(C5H9NO)nOH. CCC1=NCCO1. InChI=1S / C5H9NO / c1-2-5-6-3-4-7-5 / h2-4H2, 1H3. NYEZZYQZRQDLEH-UHFFFAOYSA-N. | |
| Poly(2-ethyl-2-oxazoline), alkyne terminated | 2-Ethyl-2-oxazoline is an oxazoline which is used particularly as a monomer for the cationic ring-opening polymerization to poly(2-alkyloxazoline)s. This type of polymers are under investigation as readily water-soluble and biocompatible materials for biomedical applications. Uses: Polyoxazolines with alkyne end functional groups can be covalently attached to azide groups through copper-mediated ligation. polyoxazolines are biocompatible; hydrophilic; amorphous alternatives to poly(ethylene glycol). Group: Hydrophilic polymers. Alternative Names: Alkyne-PEtOx-OH. CAS No. 1171957-24-6. Molecular formula: C3H3(C5H9NO)nOH. Mole weight: average Mn 10,000. Catalog: ACM1171957246-1. | |
| Poly(2-ethyl-2-oxazoline), alkyne terminated | 2-Ethyl-2-oxazoline is an oxazoline which is used particularly as a monomer for the cationic ring-opening polymerization to poly(2-alkyloxazoline)s. This type of polymers are under investigation as readily water-soluble and biocompatible materials for biomedical applications. Uses: Polyoxazolines with alkyne end functional groups can be covalently attached to azide groups through copper-mediated ligation. polyoxazolines are biocompatible; hydrophilic; amorphous alternatives to poly(ethylene glycol). Group: Hydrophilic polymers. Alternative Names: Alkyne-PEtOx-OH. CAS No. 1171957-24-6. Pack Sizes: Packaging 500 mg in glass bottle. Molecular formula: average Mn 10,000. Mole weight: C3H3(C5H9NO)nOH. | |
| Poly(2-ethyl-2-oxazoline), α-benzyl, ω-thiol terminated | 2-Ethyl-2-oxazoline is an oxazoline which is used particularly as a monomer for the cationic ring-opening polymerization to poly(2-alkyloxazoline)s. This type of polymers are under investigation as readily water-soluble and biocompatible materials for biomedical applications. Uses: Poly(2-ethyl-2-oxazoline) is a hydrophilic polymer that is commonly used in biomedical s. this is a biocompatible polymer with one chain-end functionalized with a thiol group which is commonly used in ligation as well as in thiol-ene click chemistry. these polymers are commonly used as an amorphous alternative to pegs. Group: Hydrophilic polymers. Alternative Names: Polyoxazoline, PEtOx, POx. Pack Sizes: Packaging 5 g in glass bottle. Molecular formula: average Mn 10,000. Mole weight: C6H5CH2(C5H9NO)nSH. | |
| Poly(2-ethyl-2-oxazoline) α-methyl, ω-2-hydroxyethylamine terminated | 2-Ethyl-2-oxazoline is an oxazoline which is used particularly as a monomer for the cationic ring-opening polymerization to poly(2-alkyloxazoline)s. This type of polymers are under investigation as readily water-soluble and biocompatible materials for biomedical applications. Uses: Amine polyoxazolines can be covalently attached through conjugation to carboxyl groups or sulfhydryl groups. amines can also attach to oxidized carbohydrate groups (usually aldehydes) by reductive amination. polyoxazolines are a biocompatible, hydrophilic, amorphous alternatives to poly(ethylene glycol). Group: Hydrophilic polymers. Alternative Names: aminoPEOx, Poly(2-ethyl-2-oxazoline) hydroxyethyl amine, POZ, Polyoxazoline, amino terminated polyoxazoline. Pack Sizes: Packaging 1 g in glass bottle. Molecular formula: average Mn 2,000. Mole weight: CH3(C5H9NO)nNHC2H4OH. | |
| Poly(acrylamide-co-diallyldimethylammonium chloride) solution | The hydrophilic polymer contains polar or charged functional groups, making it soluble in water. Uses: Waste treatment for laundry, emulsion breaking, sludge dewatering and drainage and retention aid. cationic polyelectrolyte. Group: Hydrophilic polymersself-assembly materials polymers. Alternative Names: P(AAm-co-DADMAC). CAS No. 26590-05-6. Pack Sizes: Packaging 1 L in poly bottle. Product ID: dimethyl-bis(prop-2-enyl)azanium; prop-2-enamide; chloride. Molecular formula: 232.75g/mol. Mole weight: C11H21ClN2O. C[N+](C)(CC=C)CC=C.C=CC(=O)N.[Cl-]. 1S/C8H16N.C3H5NO.ClH/c1-5-7-9(3, 4)8-6-2;1-2-3(4)5;/h5-6H, 1-2, 7-8H2, 3-4H3;2H, 1H2, (H2, 4, 5);1H/q+1;;/p-1. XFOSBZOUUACCCN-UHFFFAOYSA-M. | |
| Poly(allylamine) solution | Polyallylamine hydrochloride is a cationic polyelectrolyte prepared by the polymerization of allylamine. Uses: Soluble in water, lower alcohols, ethylene glycol and formamide. Group: Hydrophilic polymers. Alternative Names: PAH. CAS No. 30551-89-4. Pack Sizes: Packaging 1, 5, 25 g in poly bottle. Product ID: prop-2-en-1-amine. Molecular formula: average Mw ~15,000. Mole weight: [CH2CH(CH2NH2)]n. NCC=C. 1S/C3H7N/c1-2-3-4/h2H,1,3-4H2. VVJKKWFAADXIJK-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. | |
| 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 | 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. | |
| Polymethacrylamidopropyltrimonium Chloride | Use as antistatic agent. Use as emulsifying agent, dispersing agent. Use as flocculant. Use as film-forming agent. Use as thickening agent. Group: Cationic surfactants. Alternative Names: 3-Methacrylamidopropyltrimethylammonium chloride, homopolymer;1-Propanaminium, N,N,N-trimethyl-3-((2-methyl-1-oxo-2-propenyl)amino)-, chloride, homopolymer. CAS No. 68039-13-4. Catalog: ACM68039134. | |
| Polyquaternium-32 | Polyquaternium-32 is a cationic copolymer and is used in the treatment of coal slurry wastewater. Group: Heterocyclic organic compound. Alternative Names: N,N,N-Trimethyl-2-[(2-methyl-1-oxo-2-propenyl)oxy]ethanaminium Chloride Polymer With 2-Propenamide; (2-Methacryloyloxyethyl) trimethylammonium Chloride-Acrylamide Copolymer; (Methacryloxyethyl)trimethylammonium Chloride-acrylamide Polymer; Acrylamide Dimethylaminoethyl Methacrylate Methyl Chloride Quaternized Salt Polymer; Acrylamide- (2-methacryloyloxyethyl) trimethylammonium Chloride Copolymer;_x000B_Acrylamide-2-(dimethylamino)ethyl Methacrylate Methyl Chloride Copolymer; Acrylamide-2-(trimethylammonio)ethyl Methacrylate Chloride Copolymer; Acrylamide-2-methacryloxyethyltrimethylammonium Chloride Copolymer; Acrylamide-2-methacryloylethyl trimethyl Ammonium Chloride Copolymer; Acrylamide-N,N,N-trimethylaminoethyl Methacrylate Chloride Copolymer; Acrylamide-N,N-dimethylaminoethyl Methacrylate Meth. CAS No. 35429-19-7. Molecular formula: (C12H23ClN2O3)x. Mole weight: x(278.78). IUPACName: prop-2-enamide;trimethyl-[2-(2-methylprop-2-enoyloxy)ethyl]azanium;chloride. Canonical SMILES: CC(=C)C(=O)OCC[N+](C)(C)C. C=CC(=O)N. [Cl-]. Density: g/cm³. Catalog: ACM35429197. | |
| Polyquaternium-32 | Polyquaternium-32. Uses: Polyquaternium-32 is a cationic copolymer and is used in the treatment of coal slurry wastewater. Group: Polymers. Alternative Names: N,N,N-Trimethyl-2-[(2-methyl-1-oxo-2-propenyl)oxy]ethanaminium Chloride Polymer With 2-Propenamide; (2-Methacryloyloxyethyl) trimethylammonium Chloride-Acrylamide Copolymer; (Methacryloxyethyl)trimethylammonium Chloride-acrylamide Polymer; Acrylamide Dimethylaminoethyl Methacrylate Methyl Chloride Quaternized Salt Polymer; Acrylamide- (2-methacryloyloxyethyl) trimethylammonium Chloride Copolymer; _x005f_x005f_x005f_x005f_x000b_Acryl amide -2- (di methyl amino) ethyl Methacrylate Methyl Chloride Copolymer; Acrylamide-2-(trimethylammonio)ethyl Methacrylate Chloride Copolymer; _x000b_Acrylamide-2-methacryloxyethyltrimethylammonium Chloride Copolymer; _x000b_Acrylamide-2-methacryloylethyl trimethyl Ammonium Chloride Copolymer; Acrylamide-N,N,N-trimethylaminoethyl Methacrylate Chloride Copolymer; Acrylamide-N,N-dimethylaminoethyl Methacrylate Meth. CAS No. 35429-19-7. Product ID: prop-2-enamide; trimethyl-[2-(2-methylprop-2-enoyloxy)ethyl]azanium; chloride. Molecular formula: x(278.78). Mole weight: (C12H23ClN2O3)x. CC(=C)C(=O)OCC[N+](C)(C)C. C=CC(=O)N. [Cl-]. InChI=1S/C9H18NO2. C3H5NO. ClH/c1-8(2)9(11)12-7-6-10(3, 4)5; 1-2-3(4)5; /h1, 6-7H2, 2-5H3; 2H, 1H2, (H2, 4, 5); 1H/q+1; ; /p-1. QWMYWGHYRCRBFI-UHFFFAOYSA-M. | |
| Polyquaternium 37 | Polyquaternium-37 is a cationic polymer commonly used in hair conditioner. Polyquaternium-37 is a bactericidal polymer grafted on brushes. Group: Biochemicals. Grades: Highly Purified. CAS No. 26161-33-1. Pack Sizes: 100mg, 500mg, 1g. Molecular Formula: (C9H18ClNO2)x, Molecular Weight: 207.7. US Biological Life Sciences. | Worldwide |
| Polyquaternium-7 | Low acrylamide, non-paraben, aqueous, cationic copolymer developed for improved compatibility and clarity in anionic surfactant systems. Solids: 8-10%. Viscosity 7,500-15,000 mPas. Uses: Hair conditioners, shampoos, hair rinses, spritzes, mousse, leave-on spritzes. Group: Biomaterials. Alternative Names: 2-Propen-1-aminium,N,N-dimethyl-N-2-propenyl-,chloride,polymerwith2-propenamide. CAS No. 26590-05-6/7732-18-5/532-32-1. Molecular formula: C11H21ClN2O. Mole weight: 232.75. Appearance: Clear colorless liquid, characteristic faint odor. IUPACName: dimethyl-bis(prop-2-enyl)azanium;prop-2-enamide;chloride. Canonical SMILES: C[N+](C)(CC=C)CC=C.C=CC(=O)N.[Cl-]. Density: 1.02 (10% aq.). ECNumber: 607-965-2. Catalog: ACM26590056. | |
| Polyquaternium-7 | Low acrylamide, non-paraben, aqueous, cationic copolymer developed for improved compatibility and clarity in anionic surfactant systems. Solids: 8-10%. Viscosity 7,500-15,000 mPas. Uses: Hair conditioners, shampoos, hair rinses, spritzes, mousse, leave-on spritzes. Group: Polymers. Alternative Names: 2-Propen-1-aminium,N,N-dimethyl-N-2-propenyl-,chloride,polymerwith2-propenamide. CAS No. 26590-05-6/7732-18-5/532-32-1. Pack Sizes: 1 kg/bag,25 kg/bag or as your requirements. Product ID: dimethyl-bis(prop-2-enyl)azanium; prop-2-enamide; chloride. Molecular formula: 232.75. Mole weight: C11H21ClN2O. C[N+](C)(CC=C)CC=C.C=CC(=O)N.[Cl-]. InChI=1S/C8H16N. C3H5NO. ClH/c1-5-7-9(3, 4)8-6-2; 1-2-3(4)5; /h5-6H, 1-2, 7-8H2, 3-4H3; 2H, 1H2, (H2, 4, 5); 1H/q+1; ; /p-1. XFOSBZOUUACCCN-UHFFFAOYSA-M. | |
| Polyquaternium 77 | Polyquaternium-77 is a water-soluble, cationic polymer that is commonly used as a conditioning agent in hair care products. It works by reducing static electricity, improving hair manageability and detangling, enhancing shine, and reducing frizz. It has a positive charge that helps it attach to negatively charged hair strands. It is especially effective in curly hair, where it can help define and hold curls. Additionally, it can provide some protection against heat damage from styling tools like blow dryers or flat irons. Uses: 1. hair care: polyquaternium 77 is commonly used in hair care products, such as shampoos, conditioners, and hair styling products. it helps to improve the texture and manageability of hair, while also reducing static and frizz. 2. skin care: polyquaternium 77 can also be found in some skin care products, such as lotions and creams. it acts as a moisturizer, helping to keep skin hydrated and soft. Group: Cationic surfactants & conditioning agents. CAS No. 1309865-11-9. Appearance: clear, colorless to pale yellow liquid with a mild odor. Catalog: CI-HC-0055. | |
| Polyquaternium 81 | Polyquaternium 81 is a type of synthetic polymer that is commonly used in hair care products such as shampoos, conditioners, and styling products. It is derived from a quaternary ammonium compound and is designed to help improve the texture, feel, and manageability of hair. Polyquaternium 81 is often used as a conditioning agent and can help to detangle hair, reduce frizz, and enhance shine. It is also known to provide some level of protection against damage from heat styling tools and other environmental factors. Uses: 1. hair care: polyquaternium 81 is commonly used as a conditioning agent in hair care products like shampoos, conditioners, and styling products to improve the softness and manageability of hair. 2. skin care: it is also utilized in skin care products like moisturizers and lotions to enhance skin moisturization as well as provide a silky smooth feel. 3. sunscreen: polyquaternium 81 also provides t. Group: Cationic surfactants & conditioning agents. CAS No. 1309865-12-0. Catalog: CI-HC-0056. | |
| Triethylsilane 99+% (GC) | Triethylsilane is a trialkylsilicon hydride used in the synthesis of alkylsilanes via hydrosilation of olefins. Triethylsilane is also used as an effective reducing agent. It acts as a reducing agent in the reduction of 2-chromanols, since it has an active hydride. It acts as a catalyst for redox initiated cationic polymerization, regioselective reductive coupling of enones and allenes, and Beckmann rearrangement of cyclododecanone oxime. It is associated with trifluoroacetic acid and involved in the selective reduction of alkenes. Group: Biochemicals. Alternative Names: NSC 93579; Triethylhydrosilane; Triethylsilicon hydride. Grades: GC. CAS No. 617-86-7. Pack Sizes: 25g, 100g, 250g, 1Kg, 2.5Kg. US Biological Life Sciences. | Worldwide |
| Zephirol Related Compound 3 | One of the impurities of Zephirol, a quaternary ammonium compound, has been found to be effective in the treatment of herpes, hepatitis and other infections. Uses: Used as a cationic surfactant, wetting agent, emulsifier, germicide, fungicide, disinfectant, and slimicide; used in industrial cleaners, emulsion polymerization processes, paper and textile processing, hair colors and conditioners (softener), lipsticks and lotions (emollient), textiles (softener), hair sprays (antistatic agent), and contraceptive formulations; quaternary ammonium compounds are also used as algaecides/slimicides (swimming pools, industrial water reservoirs, and farm ponds), antiseptics for cleaning wounds, antistatic agents for textiles, softeners for paper products, and pigment dispersers. Synonyms: N,N-Dimethyl-N-octadecylbenzenemethanaminium Chloride; Benzyldimethyloctadecylammonium Chloride; Algene SC 25; Carsoquat SDQ 25; Stebac; Triton CG 500; Varisoft SDC. Grades: >98.0%(T). CAS No. 122-19-0. Molecular formula: C27H50N.Cl. Mole weight: 424.15. |  |
| 1,10-Diiododecane | 1,10-Diiododecane is an intermediate in the synthesis of Dequalinium Chloride (D288335) which is a quaternary ammonium cation and the active ingredient in various medications including antiseptic and anti-malarial agents. It was also used in synthesis of a dyeing photoinitiator system for acrylate monomer polymerization. Group: Biochemicals. Grades: Highly Purified. CAS No. 16355-92-3. Pack Sizes: 1g, 5g. Molecular Formula: C10H20I2, Molecular Weight: 394.07. US Biological Life Sciences. | Worldwide |
| 1,2-Dihexadecanoyl-rac-glycero-3-phospho-rac-(1-glycerol) Ammonium Salt | 1,2-Dihexadecanoyl-rac-glycero-3-phospho-rac-(1-glycerol) shows strong interaction with the cationic antibiotic polymyxin B. Group: Biochemicals. Grades: Highly Purified. CAS No. 73548-70-6. Pack Sizes: 25mg, 100mg. Molecular Formula: C38H78NO10P, Molecular Weight: 740. US Biological Life Sciences. | Worldwide |
| 1,4,7,10-Tetraazacyclododecane | Macrocyclic aza analogue of the crown ether 12-crown-4. Cyclen compounds are capable of selectively binding cations and are used as a ligand with chemicals used in MRI contrast (as well ass other imaging) agents. Group: Polymer/macromolecule. Alternative Names: MLS000069489; Cyclen, 97%; AJ-75747; BP-21532; CHEBI:37391; KRYPTOFIX 11 AZA; EC 425-450-9; 964584YO2O; AM20090388; NCGC00018128-02. CAS No. 294-90-6. Molecular formula: C8H20N4. Mole weight: 172.276g/mol. IUPACName: 1,4,7,10-tetrazacyclododecane. Canonical SMILES: C1CNCCNCCNCCN1. ECNumber: 425-450-9. Catalog: ACM294906. | |
| Baloxavir | Baloxavir marboxil is a first-in-class, one-dose oral medicine with a novel proposed mechanism of action that has demonstrated efficacy in a wide range of influenza viruses, including in vitro activity against oseltamivir-resistant strains and avian strains (H7N9, H5N1) in non-clinical studies. Baloxavir is a polymerase acidic, cap-dependent, endonuclease inhibitor that is indicated for the treatment of acute uncomplicated influenza in patients aged 12 years and older who have been symptomatic for no more than 48 hours. It blocks viral proliferation by binding to one of two endonuclease binding sites, inhibiting the initiation of mRNA synthesis for both influenza A and influenza B strains. Baloxavir can interact with polyvalent cation-containing products, which can decrease its plasma concentration. Synonyms: Baloxavir acid; BXA; Xofluza; S-033447. Grades: ≥98%. CAS No. 1985605-59-1. Molecular formula: C24H19F2N3O4S. Mole weight: 483.49. | |
| Baloxavir marboxil | Baloxavir marboxil is a first-in-class, one-dose oral medicine with a novel proposed mechanism of action that has demonstrated efficacy in a wide range of influenza viruses, including in vitro activity against oseltamivir-resistant strains and avian strains (H7N9, H5N1) in non-clinical studies. Baloxavir is a polymerase acidic, cap-dependent, endonuclease inhibitor that is indicated for the treatment of acute uncomplicated influenza in patients aged 12 years and older who have been symptomatic for no more than 48 hours. It blocks viral proliferation by binding to one of two endonuclease binding sites, inhibiting the initiation of mRNA synthesis for both influenza A and influenza B strains. Baloxavir can interact with polyvalent cation-containing products, which can decrease its plasma concentration. Synonyms: S-033188; HY-109025. Grades: ≥98%. CAS No. 1985606-14-1. Molecular formula: C27H23F2N3O7S. Mole weight: 571.55. | |
| Cationic Polyacrylamide | Acrylamide appears as white crystalline solid shipped either as a solid or in solution. A confirmed carcinogen. Toxic by skin absorption. Less dense than water and soluble in water. May be toxic by ingestion. Used for sewage and waste treatment, to make dyes, adhesives. The solid is stable at room temperature, but upon melting may violently polymerize. Toxic, irritating to skin, eyes, etc.;Acrylamide solution, [aqueous] appears as a colorless aqueous solution of a solid. Often at a concentration of 40% (w/v). Spills can easily penetrate the soil and contaminate groundwater and nearby streams. Used for sewage and waste treatment and to make dyes and adhesives. Toxic, irritating to skin, eyes, etc. Produce toxic oxides of nitrogen when burned.;Acrylamide solution, [flammable liquid label] appears as a solution of a colorless crystalline solid. Flash point depends on the solvent but below 141°F. Less dense than water. Vapors heavier than air. Toxic oxides of nitrogen produced during combustion. Used for sewage and waste treatment, to make dyes and adhesives.;DryPowder; Liquid; OtherSolid;Solid;WHITE CRYSTALS.;White crystalline, odorless solid.;White crystalline, odorless solid. Group: other nano materials. CAS No. 9003-5-8. Product ID: prop-2-enamide. Molecular formula: 3-16 Million (adjustable). Mole weight: C3H5NO. C=CC(=O)N. 99.9%. | |
| Cationic Polyacrylamide | Acrylamide appears as white crystalline solid shipped either as a solid or in solution. A confirmed carcinogen. Toxic by skin absorption. Less dense than water and soluble in water. May be toxic by ingestion. Used for sewage and waste treatment, to make dyes, adhesives. The solid is stable at room temperature, but upon melting may violently polymerize. Toxic, irritating to skin, eyes, etc.;Acrylamide solution, [aqueous] appears as a colorless aqueous solution of a solid. Often at a concentration of 40% (w/v). Spills can easily penetrate the soil and contaminate groundwater and nearby streams. Used for sewage and waste treatment and to make dyes and adhesives. Toxic, irritating to skin, eyes, etc. Produce toxic oxides of nitrogen when burned.;Acrylamide solution, [flammable liquid label] appears as a solution of a colorless crystalline solid. Flash point depends on the solvent but below 141°F. Less dense than water. Vapors heavier than air. Toxic oxides of nitrogen produced during combustion. Used for sewage and waste treatment, to make dyes and adhesives.;DryPowder; Liquid; OtherSolid;Solid;WHITE CRYSTALS.;White crystalline, odorless solid.;White crystalline, odorless solid. Group: Polymers. CAS No. 9003-5-8. Product ID: prop-2-enamide. Molecular formula: 3-16 Million (adjustable). Mole weight: C3H5NO. C=CC(=O)N. InChI=1S/C3H5NO/c1-2-3(4)5/h2H, 1H2, (H2, 4, 5). HRPVXLWXLXDGHG-UHFFFAOYSA-N. 99.9%. | |
| Macroporous weakly acid cation exchange resins, AR | Macroporous weakly acid cation exchange resins, AR. Group: Polymers. | |
| Native Avian myeloblastosis virus AMV-Reverse Transcriptase | A Reverse transcriptase (RT) is an enzyme used to geneRate complementary DNA (cDNA) from an RNA template, a process termed reverse transcription. It is mainly associated with retroviruses. However, non-retroviruses also use RT (for example, the hepatitis B virus, a member of the Hepadnaviridae, which are dsDNA-RT viruses, while retroviruses are ssRNA viruses). RT inhibitors are widely used as antiretroviral drugs. RT activities are also associated with the replication of chromosome ends (telomerase) and some mobile genetic elements (retrotransposons). Applications: Amv reverse transcriptase synthesizes dna complementary (cdna) to rna templates. a dna primer complementary to the rna template and a divalent cation, either mg or mn, are required for initiation of transcription. this enzyme is commonly used to make cdnas from mrna for eventual cloning or for use as probes. Group: Enzymes. Synonyms: DNA nucleotidyltransferase (RNA-directed); reverse transcripta. Enzyme Commission Number: EC 2.7.7.49. CAS No. 9068-38-6. RT. Storage: -70°C. Source: Avian myeloblastosis virus. DNA nucleotidyltransferase (RNA-directed); reverse transcriptase; revertase; RNA-dependent deoxyribonucleate nucleotidyltransferase; RNA revertase; RNA-dependent DNA polymerase; RNA-instructed DNA polymerase; RT; EC 2.7.7.49; 9068-38-6. Cat No: NATE-0073. |  |
| Native Bovine Protein Phosphatase 2A1 | Protein Phosphatase 2A1 is a trimer consisting of the A, B, and C subunits of the PP2A family. It has a total molecular weight of 192 kDa. Protein Phosphatase 2A is a cytoplasmic protein, which colocalizes with mictotubule proteins and is involved in the dephosphorylation of the tau protein and oncoprotein 18. Protein Phosphatase 2A1 binds to polymerized microtubule proteins and may be targeted by tubulin in modulating phosphatase activity. Applications: Protein phosphatase 2a1 is a divalent cation-dependent protein serine/threonine phosphatase implicated as a growth suppressor and is associated with dis-regulation in cancer. the enzyme is involved in regulating numerous cellular processes and is used to study cell cycle, growth, and differentiation. the protein phosphatase 2a1 has been used to treat human fibroblast cells prior to western blot analysis. Group: Enzymes. Synonyms: Protein Phosphatase 2A1; PP2A1; PPA2A1. Purity: >90% (SDS-PAGE). Protein Phosphatase. Activity: > 1500 units/mg protein. Stability: -70°C. Form: Solution in 50 mM Tris-HCl, pH 7.0, containing 14 mM 2-mercaptoethanol, 1 mM benzamidine, 0.1 mM PMSF, 1 mM EDTA, and 50% glycerol. Source: Bovine. Protein Phosphatase 2A1; PP2A1; PPA2A1. Pack: vial of 1 μg. Cat No: NATE-0616. | |
| Polymyxin B nonapeptide acetate | Polymyxin B nonapeptide acetate is a cationic cyclic peptide that interacts with the outer membrane of gram-negative bacteria to increase the permeability of the membrane by promoting hydrophobic diffusion. Synonyms: H-Thr-Dab-Dab-Dab-D-Phe-Leu-Dab-Dab-Thr.CH3CO2H (Disulfide bridge: Cys3-Cys9); Polymyxin B1, 1-de[N2-(6-methyl-1-oxooctyl)-L-2,4-diaminobutanoic acid]-, acetate; 2-10-Polymyxin B1 acetate. Grades: ≥95%. Molecular formula: C45H78N14O13. Mole weight: 1023.19. | |
| Polymyxin B Sulfate USP (Bacillus polymyxa prazmowski migula, Aerosporin) | Antibiotic which inhibits PKC via bacterial membrane binding mechanism. Effective against gram negative bacteria. Polymyxins bind to the cell membrane and alter its structure making it more permeable. The resulting water uptake leads to cell death. They are cationic, basic proteins that act like detergents (surfactants}. Side effects include neurotoxicity and acute renal tubular necrosis. it is commonly used in the topical first aid preparation Neosporin. Polymyxin B belongs to a family of polypeptides with attached fatty acid, acting as a cationic detergent at physiological pH, both hydrophilic and hydrophobic properties. Polymyxin B is bactericidal for gram-negative, and has little to no effect on gram-positive since cell wall is too thick to permit access to membrane. Group: Biochemicals. Alternative Names: Bacillus polymyxa prazmowski migula, Aerosporin. Grades: Cell Culture Grade. CAS No. 1405-20-5. Pack Sizes: 10MU, 50MU, 100MU. US Biological Life Sciences. | Worldwide |
| Poly(sodium 4-styrenesulfonate) | Poly (sodium 4-styrenesulfonate) is a cation exchange polyelectrolyte used to prepare highly mechanically stable and highly reproducible coatings. During the reduction of graphene oxide, Poly (sodium 4-styrenesulfonate) is used to synthesize polymer-coated graphite nanosheets. Furthermore, the interactions between Poly (sodium 4-styrenesulfonate) and metal ions have been studied, and it has been combined with Nafion for mixed coatings in bismuth film electrodes, showcasing its broad application potential in functional materials and electrochemical research [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 25704-18-1. Pack Sizes: 1 mg. Product ID: HY-W739372. | |
| Poly(vinylsulfonic acid, sodium salt) solution | Poly(vinylsulfonic acid, sodium salt) is a polymer that consists of repeating units of vinylsulfonic acid monomers, where each vinylsulfonic acid unit is neutralized with a sodium cation (Na+). Poly(vinylsulfonic acid, sodium salt) is an example of a polyelectrolyte, which is a type of polymer that contains ionizable groups along its chain. The presence of sulfonic acid groups (-SO3H) in this polymer provides it with strong acidic properties. However, when the polymer is neutralized with sodium ions, it becomes water-soluble and exhibits enhanced solubility and stability in aqueous solutions. Uses: Poly(vinylsulfonicacid, sodium salt) (pvsa) can be used: in the preparation of superabsorbent semi-ipn (interpenetrating polymer network) hydrogel. as a solid electrolyte for proton conduction in the fabrication of an all-solid-supercapacitor. as a crystallization controlling agent in the preparation of high-quality crystals of porous coordination polymers(cp). pvsa regulates not only the size and structure of the crystals but also their preference orientation, resulting in cp channel alignment in the bulk powdery state. Alternative Names: PVSA. CAS No. 9002-97-5. Molecular formula: (C2H3NaO3S)n. Mole weight: 130.098. Appearance: Liquid. Purity: 0.75. Canonical SMILES: [Na]OS(=O)(=O)C=C. Density: 1.267 g/mL at 25ºC. Catalog: ACM9002975. | |
| SPR741 | SPR741 is a cationic peptide derived from polymyxin B and is a potentiator molecule. SPR741 inhibits multidrug-resistant Gram-negative bacteria. The spectrum of activity of the antibiotic can be widened when used in combination with SPR741 TFA. Synonyms: NAB741. Grades: >98%. CAS No. 1179330-52-9. Molecular formula: C44H73N13O13. Mole weight: 992.13. | |
| Strong Acidic Cation Resins | Strong Acidic Cation Resins. Group: Polymers. | |
| Tetraoctylammonium bromide | Tetraoctylammonium bromide (TOAB) is a quaternary ammonium salt consisting of a positively charged tetraoctylammonium cation and a negatively charged bromide anion. This compound is commonly used as a phase transfer catalyst in organic chemical reactions, facilitating the transfer of reactants between immiscible phases. It is also used as a surfactant and dispersant in various industrial applications, for example in the production of coatings, adhesives and polymers. Additionally, Tetraoctylammonium bromide has been investigated for potential applications in energy storage devices and as an antimicrobial agent. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 14866-33-2. Pack Sizes: 500 g. Product ID: HY-W018574. | |
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