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| Product | Description | |
|---|---|---|
| Alkyl phenol ethoxylates | Our wide distribution network, with locations coast-to-coast, helps guarantee fast, reliable service to Univar's customers. |  |
| ALKYL PHENOLIC RESIN | ALKYL PHENOLIC RESIN. Group: Polymers. |  |
| Alkylphenol disulfide | Alkylphenol disulfide. Group: Polymers. Alternative Names: ALKYLPHENOL DISULFIDE; PTBP-formaldehyde resins; p-tert-Butylphenol-formaldehyde resins; Formaldehyde, polymer with 4-(1,1-dimethylethyl)phenol; PTBPFRESIN; PARA-TERTIARYBUTYLPHENOLFORMALDEHYDERESIN; PTBPF; BPF-RESIN. CAS No. 25085-50-1. Product ID: 4-tert-butylphenol; formaldehyde. Molecular formula: 180.24g/mol. Mole weight: C11H16O2. CC(C)(C)C1=CC=C(C=C1)O.C=O. InChI=1S/C10H14O.CH2O/c1-10(2, 3)8-4-6-9(11)7-5-8;1-2/h4-7, 11H, 1-3H3;1H2. LZDOYVMSNJBLIM-UHFFFAOYSA-N. | |
| (1S,2S)-(+)-[1,2-Cyclohexanediamino-N,N'-bis(3,5-di-t-butylsalicylidene)]chromium(III) chloride | Catalyst for the asymmetric ring-opening of meso-epoxides and for the kinetic resolution of terminal epoxides. Precatalyst for asymmetric Diels-Alder and hetero Diels-Alder reactions. Catalyst for copolymerization of CO2 and epoxides. Catalyst for enantioselective alkylation of tributyltin enolates. Enantioselective addition of Me2Zn to aldehydes. Enantioselective intramolecular addition of tertiary enamides to ketones. Asymmetric iodocyclization. Catalytic intermolecular linear allylic C-H animation. Cocatalyst for enantioselective ring opening of epoxides with fluoride. Group: Heterocyclic organic compound. Alternative Names: SCHEMBL2189792;219143-92-7;(S,S)-N,N -Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminochromium(III) chloride. CAS No. 219143-92-7. Molecular formula: C36H54ClCrN2O2-. Mole weight: 634.286g/mol. IUPACName: chromium; 2, 4-ditert-butyl-6- [ [ (1S, 2S) -2- [ (3, 5-ditert-butyl-2-hydroxyphenyl) methylideneamino] cyclohexyl] iminomethyl] phenol; chloride. Canonical SMILES: CC (C) (C)C1=CC (=C (C (=C1)C=NC2CCCCC2N=CC3=CC (=CC (=C3O)C (C) (C)C)C (C) (C)C)O)C (C) (C)C. [Cl-]. [Cr]. ECNumber: 606-861-4. Catalog: ACM219143927. |  |
| 2-(2-Heptynylthio)-phenol Acetate (APHS) | An O-acetyl, S-alkyl thio ether of 2-thio phenol. It is a potent i. Group: Biochemicals. Alternative Names: APHS. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. |  Worldwide |
| 2,6-Di-tert-butylphenol | 26-Di-tert-butylphenol is an organic compound with the structural formula 2,6-((CH3)3C)2C6H3OH. This colorless solid alkylated phenol and its derivatives are used industrially as UV stabilizers and Antioxidants for hydrocarbon-based products ranging from petrochemicals to plastics. Illustrative of its usefulness, it prevents gumming in aviation fuels. Group: Plastic additives. Alternative Names: 2,6-Di-t-butylphenol. CAS No. 128-39-2. Product ID: 2,6-ditert-butylphenol. Molecular formula: 206.32. Mole weight: C14H22O. CC(C)(C)C1=C(C(=CC=C1)C(C)(C)C)O. InChI=1S/C14H22O/c1-13(2, 3)10-8-7-9-11(12(10)15)14(4, 5)6/h7-9, 15H, 1-6H3. DKCPKDPYUFEZCP-UHFFFAOYSA-N. | |
| 4,4'-(1,2-Diphenylethene-1,2-diyl)diphenol | 4,4'-(1,2-Diphenylethene-1,2-diyl)diphenol. Uses: Tpe-doh is a synthetic intermediate of aggregation-induced emission (aie) dye for use in further synthesis of alkyl-halogen to make ether and polymer reaction via esterification. Group: Synthetic tools and reagents. Alternative Names: 1,2-Bis(4-hydroxyphenyl)-1,2-diphenylethylene,4,4'-(1,2-Diphenyl-1,2-ethenediyl)bisphenol,TPE-DOH. CAS No. 68578-79-0. Pack Sizes: 25 mg in poly bottle. Product ID: 4-[(E)-2-(4-hydroxyphenyl)-1,2-diphenylethenyl]phenol. Molecular formula: 364.44. Mole weight: C26H20O2. OC (C=C1)=CC=C1/C (C2=CC=CC=C2)=C (C3=CC=CC=C3)/C4=CC=C (O)C=C4. 1S/C26H20O2/c27-23-15-11-21 (12-16-23)25 (19-7-3-1-4-8-19)26 (20-9-5-2-6-10-20)22-13-17-24 (28)18-14-22/h1-18, 27-28H/b26-25+, ZYIGFXHZSKIVOO-OCEACIFDSA-N. ZYIGFXHZSKIVOO-OCEACIFDSA-N. | |
| 4,4',4'',4'''-(Ethene-1,1,2,2-tetrayl)tetraphenol | 4,4',4'',4'''-(Ethene-1,1,2,2-tetrayl)tetraphenol. Uses: Tpe-toh is a synthetic intermediate of aggregation-induced emission (aie) dye for use in further synthesis of alkyl-halogen to make ether via esterification and polymer reaction. Group: Bioelectronic materials organic light-emitting diode (oled) materials other materials. Alternative Names: 4,4',4'',4'''-(1,2-Ethenediylidene)tetrakisphenol,TPE-TOH,Tetra(4-hydroxyphenyl)ethylene. CAS No. 119301-59-6. Pack Sizes: 25 mg in glass insert. Product ID: 4-[1,2,2-tris(4-hydroxyphenyl)ethenyl]phenol. Molecular formula: 396.43. Mole weight: C26H20O4. OC (C=C1)=CC=C1C (C2=CC=C (O)C=C2)=C (C3=CC=C (O)C=C3)C4=CC=C (O)C=C4. 1S/C26H20O4/c27-21-9-1-17 (2-10-21)25 (18-3-11-22 (28)12-4-18)26 (19-5-13-23 (29)14-6-19)20-7-15-24 (30)16-8-20/h1-16, 27-30H, QQUZHNPGWNIYMK-UHFFFAOYSA-N. QQUZHNPGWNIYMK-UHFFFAOYSA-N. | |
| Nonoxinol 15 | Nonoxinol 15. Synonyms: Nonoxynol-15; polyoxyethylene nonylphenol ether; NP-15; Nonyl phenol ether; Nonyl Phenol Ethyleneoxide. CAS No. 26027-38-3. Product ID: PE-0624. Molecular formula: C9H19C6H4(OCH2CH2)nOH (n=15). Mole weight: 885.17. Category: Surfactant. Product Keywords: Excipients for Liquid Dosage Form; Surfactant Excipients; PE-0624; Nonoxinol 15; Surfactant; C9H19C6H4(OCH2CH2)nOH (n=15); 26027-38-3. UNII: 5V4827GL2O. Chemical Name: α -(p-Nonylphenyl)-ω -hydroxynona(oxyethylene). Grade: Pharmceutical Excipients. Administration route: Inhalant oral, topical. Dosage Form: Local administration solution; Local sponge; Ordinary topical preparations. Stability and Storage Conditions: Gradually saponification under strong acid or base conditions; Stable in a weak acid or base. Store in an airtight container in a cool and dry place. Commonly used amount and the maximum amount: Local sponge: 50.50mg; Topical solution: 5.05%. Source and Preparation: It is an admixture of nonanphenol and ethylene oxide, and its alkyl carbon number is about 15. Applications: Surfactant, spermicide. |  |
| Nonoxinol 4 | Nonoxinol 4. Synonyms: Nonoxynol-4; polyoxyethylene nonylphenol ether; NP-4; Nonyl phenol ether; Nonyl Phenol Ethyleneoxide. CAS No. 26027-38-3. Product ID: PE-0625. Molecular formula: C9H19C6H4(OCH2CH2)nOH (n=4). Mole weight: 616.87. Category: Surfactant. Product Keywords: Excipients for Liquid Dosage Form; Surfactant Excipients; PE-0625; Nonoxinol 4; Surfactant; C9H19C6H4(OCH2CH2)nOH (n=4); 26027-38-3. UNII: 48Q180SH9T. Chemical Name: α -(p-Nonylphenyl)-ω -hydroxynona(oxyethylene). Grade: Pharmceutical Excipients. Stability and Storage Conditions: Gradually saponification under strong acid or base conditions; Stable in a weak acid or base. Store in an airtight container in a cool and dry place. Commonly used amount and the maximum amount: Ophthalmic solution: 0.12%; Topical solution: 0.01%. Source and Preparation: It is an admixture of nonanphenol and ethylene oxide, and its alkyl carbon number is about 4. Applications: Surfactant, spermicide. | |
| Nonoxinol 9 | Colorless to yellowish oily liquid. Synonyms: Nonoxynol-9; polyoxyethylene nonylphenol ether; NP-9; Nonyl phenol ether; Nonyl Phenol Ethyleneoxide. CAS No. 26027-38-3. Product ID: PE-0626. Molecular formula: C9H19C6H4(OCH2CH2)nOH (n=9). Mole weight: 616.82. Category: Surfactant. Product Keywords: Excipients for Liquid Dosage Form; Surfactant Excipients; PE-0626; Nonoxinol 9; Surfactant; C9H19C6H4(OCH2CH2)nOH (n=9); 26027-38-3. UNII: 48Q180SH9T. Chemical Name: α -(p-Nonylphenyl)-ω -hydroxynona(oxyethylene). Grade: Pharmceutical Excipients. Administration route: Inhalant oral, topical. Dosage Form: Local administration solution; Local sponge; Ordinary topical preparations. Stability and Storage Conditions: Gradually saponification under strong acid or base conditions; Stable in a weak acid or base. Store in an airtight container in a cool and dry place. Commonly used amount and the maximum amount: Ophthalmic solution: 0.12%; Topical solution: 0.01%. Source and Preparation: It is an admixture of nonanphenol and ethylene oxide, and its alkyl carbon number is about 9. | |
| phenol O-methyltransferase | Acts on a wide variety of simple alkyl-, methoxy- and halo-phenols. Group: Enzymes. Synonyms: PMT. Enzyme Commission Number: EC 2.1.1.25. CAS No. 37256-94-3. 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-1853; phenol O-methyltransferase; EC 2.1.1.25; 37256-94-3; PMT. Cat No: EXWM-1853. |  |
| Tyloxapol | Tyloxapol, is a nonionic liquid polymer of the alkyl aryl polyether alcohol type. It is used as a surfactant to aid liquefaction and removal of mucopurulent (containing mucus and pus) bronchopulmonary secretions. Tyloxapol also blocks plasma lipolytic activity. Group: Others. Alternative Names: Ethoxylated p-tert-octylphenol formaldehyde polymer. CAS No. 25301-02-4. Molecular formula: C8H11NO. Mole weight: 137.18. Appearance: Viscous amber liquid. Purity: 0.99. IUPACName: formaldehyde;oxirane;4-(2,4,4-trimethylpentan-2-yl)phenol. Canonical SMILES: CC(C)(C)CC(C)(C)C1=CC=C(C=C1)O. C=O. C1CO1. Catalog: ACM25301024. | |
| Tyloxapol | Tyloxapol. Uses: Tyloxapol, is a nonionic liquid polymer of the alkyl aryl polyether alcohol type. it is used as a surfactant to aid liquefaction and removal of mucopurulent (containing mucus and pus) bronchopulmonary secretions. tyloxapol also blocks plasma lipolytic activity. Group: Polymers. Alternative Names: Ethoxylated p-tert-octylphenol formaldehyde polymer. CAS No. 25301-02-4. Product ID: formaldehyde; oxirane; 4-(2,4,4-trimethylpentan-2-yl)phenol. Molecular formula: 137.18. Mole weight: C8H11NO. CC(C)(C)CC(C)(C)C1=CC=C(C=C1)O. C=O. C1CO1. InChI=1S/C14H22O.C2H4O.CH2O/c1-13(2, 3)10-14(4, 5)11-6-8-12(15)9-7-11; 1-2-3-1; 1-2/h6-9, 15H, 10H2, 1-5H3; 1-2H2; 1H2. MDYZKJNTKZIUSK-UHFFFAOYSA-N. 99%. | |
| Tyloxapol, USP | Tyloxapol is a nonionic liquid polymer of the alkyl aryl polyether alcohol type. It is used as a surfactant to aid liquefaction and removal of mucopurulent[citation needed] (containing mucus and pus) bronchopulmonary secretions,[1][2] administered by inhalation through a nebulizer[3] or with a stream of oxygen. With intraperitoneal injection, tyloxapol also blocks plasma lipolytic activity, and thus the breakdown of triglyceride-rich lipoproteins. This mechanism is used to induce experimental hyperlipidemia in animals.[4] Tyloxapol is the main active ingredient of the medical device Tacholiquin®. Tacholiquin® is an expectorant designated for inhalation and instillation reaching the upper and lower airways. Group: Biochemicals. Alternative Names: p- (1, 1, 3, 3-Tetramethylbutyl) Phenol Polymer with Ethylene Oxide and Formaldehyde; Ethylene Oxide Polymer with Formaldehyde and p- (1, 1, 3, 3-Tetramethylbutyl) phenol; Oxirane Polymer with Formaldehyde and 4- (1, 1, 3, 3-tetramethylbutyl) phenol; Ethylene oxide-formaldehyde-4- (1, 1, 3, 3-tetramethylbutyl) phenol copolymer; Ethylene oxide-formaldehyde-p-octylphenol Copolymer; NSC 90255; Superinone; Triton A 20; Triton WR 1339; Tyloxapol; p-Isooctyl polyoxyethyl ene phenol Formaldehyde Polymer. Grades: USP. CAS No. 25301-02-4. Pack Sizes: 1g, 5g, 25g. Molecular Formula: (C17H30O4)n, Molecular Weight: As reported. US Biological Life Sciences. | Worldwide |
| (Z)-1,2-Diphenyl-1-(4-hydroxyphenyl)-1-butene | A metabolite of Tamoxifen, that can be biotransformed to a quinone methide, which has the potential to alkylate DNA and may contribute to the genotoxic effects of tamoxifen. This compound slightly increases intracellular free calcium [Ca2+]i in human platelets and partially inhibits thrombin-induced [Ca2+]i elevation. Group: Biochemicals. Alternative Names: (Z)-1-(4-Hydroxyphenyl)-1,2-diphenyl-1-butene; (Z)-4-(1,2-Diphenyl-1-butenyl)phenol; ICI 141389; Des-O-dimethylaminoethyl Tamoxifen. Grades: Highly Purified. CAS No. 69967-80-2. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
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