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| Product | Description | |
|---|---|---|
| Linear Alkyl Benzene 68442-69-3 | Linear Alkyl Benzene - Surface Coatings. SUPPLIERS TO BUSINESS CUSTOMERS ONLY. |  North America & APAC |
| Benzoic acid, 2,2-(2,4(or 4,6)-dihydroxy-1,3-phenylene)bis(azo)bis-, mixed C11-14-branched and linear alkyl and 2-ethylhexyl diesters | Heterocyclic Organic Compound. Alternative Names: Benzoic acid, 2,2-(2,4(or 4,6)-dihydroxy-1,3-phenylene)bis(azo)bis-, mixed C11-14-branched and linear alkyl and 2-ethylhexyl diesters;2,2'-[(2,4(or 4,6)-Dihydroxy-1,3-phenylene)bis(azo)]bisbenzoic acid mixed C11-14 -branched and linear alkyl and 2-ethyl. CAS No. 115340-73-3. Catalog: ACM115340733. |  |
| Glycine, N-[(C10-22-branched and linear alkyl and naphthenyl)sulfonyl] derivs., compds. with morpholine (1:1) | Heterocyclic Organic Compound. Alternative Names: Glycine, N-[(C10-22-branched and linear alkyl and naphthenyl)sulfonyl] derivs., compds. with morpholine (1:1);Einecs 310-158-5;Glycine, N-((C10-22-branched and linear alkyl and naphthenyl)sulfonyl) derivs., compds. with morpholine (1:1). CAS No. 121543-32-6. Catalog: ACM121543326. | |
| Glycine, N-[(chlorinated C10-22-branched and linear alkyl and naphthenyl)sulfonyl] derivs., compds. with morpholine (1:1) | Heterocyclic Organic Compound. Alternative Names: Glycine, N-[(chlorinated C10-22-branched and linear alkyl and naphthenyl)sulfonyl] derivs., compds. with morpholine (1:1). CAS No. 121543-33-7. Catalog: ACM121543337. | |
| (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. | |
| Epicoccamide | It is an ornate linear fatty acid with an acyl tetronic acid terminus and glycosidic alkyl terminus. It is originally isolated from epicoccum purpurascens. It is non-cytotoxic, unlike the weak activity shown by related analogues Epicoccamides B, C and D. Synonyms: 5-hydroxy-1,2-dimethyl-4-(2-methyl-16-(((2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)hexadecanoyl)-1,2-dihydro-3H-pyrrol-3-one; 1,2-Dihydro-5-hydroxy-4-[16-(β-D-mannopyranosyloxy)-2-methyl-1-oxohexadecyl]-1,2-dimethyl-3H-pyrrol-3-one. Grades: >98% by HPLC. CAS No. 606139-26-8. Molecular formula: C29H51NO9. Mole weight: 557.72. |  |
| LABSA | LABSA is a clear to yellowish, viscous liquid with a strong, sulfurous smell. It is typically used as a raw material for the production of detergents, emulsifiers, and other cleaning agents. It is also used in the production of personal care products, such as shampoos and body washes, as well as in the oil and gas industry. Uses: Detergents: LABSA is a key ingredient in the production of laundry detergents, dishwashing liquids, and other cleaning agents. It helps to remove dirt, grease, and stains from surfaces and fabrics.Personal care products: LABSA is used as a surfactant in the production of personal care products such as shampoos, body washes, and shower gels. It helps to create a lather and cleanse the skin and hair.Oil and gas industry: LABSA is used in the oil and gas industry as a drilling and fracturing fluid, as well as a gelling agent in the production of drilling muds.Industrial cleaning: LABSA is used as a cleaning agent in a variety of industrial applications, including in the production of paints, inks, and other coatings.Other uses: LABSA may also be used in the production of emulsifiers, wetting agents, and other chemical intermediates. Group: surfactant. Alternative Names: Alkylbenzene sulfonic acid (ABSA)LASSodium linear alkylbenzene sulfonate (SLAS)Sodium alkylbenzene sulfonate (SAS)Linear alkylbenzene sulfonate (LAS). Grades: Technical Grade. CAS No. 85536-14-7. |  |
| Native Porcine Acylase I | In enzymology, an aminoacylase (EC 3.5.1.14) is an enzyme that catalyzes the chemical reaction:N-acyl-L-amino acid + H2O<-> carboxylate + L-amino acid. Thus, the two substRates of this enzyme are N-acyl-L-amino acid and H2O, whereas its two products are carboxylate and L-amino acid. This enzyme belongs to the family of hydrolases, those acting on carbon-nitrogen bonds other than peptide bonds, specifically in linear amides. This enzyme participates in urea cycle and metabolism of amino groups. Protein determined by biuret. Applications: Acylase i from porcine kidney has been used to study the acylase i-catalyzed deacetylation of various s-alkyl-n-acetyl-l-cysteines and their carb...ort acyl amidoacylase; ACY1 (gene name); N-acyl-L-amino-acid amidohydrolase; EC 3.5.1.14; 9012-37-7. Enzyme Commission Number: EC 3.5.1.14. CAS No. 9012-37-7. ACY1. Activity: > 2,000 units/mg protein; 500-1,500 units/mg protein. Storage: -20°C. Form: lyophilized powder. Source: Porcine kidney. Species: Porcine. aminoacylase 1; aminoacylase I; dehydropeptidase II; histozyme; hippuricase; benzamidase; acylase I; hippurase; amido acid deacylase; L-aminoacylase; acylase; aminoacylase; L-amino-acid acylase; α-N-acylaminoacid hydrolase; long acyl amidoacylase; short acyl amidoacylase; ACY1 (gene name); N-acyl-L-amino-acid amidohydrolase; EC 3.5.1.14; 9012-37-7. Cat No: NATE-0031. |  |
| N-isopropylammelide isopropylaminohydrolase | Requires Zn2+. This bacterial enzyme is involved in degradation of the herbicide atrazine. It can hydrolyse other N-substituted amino dihydroxy-s-triazine molecules, and prefers substrates with linear N-alkyl groups to those with branched alkyl groups. Group: Enzymes. Synonyms: atzC (gene name). Enzyme Commission Number: EC 3.5.4.42. CAS No. 203810-02-0. 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-4571; N-isopropylammelide isopropylaminohydrolase; EC 3.5.4.42; 203810-02-0; atzC (gene name). Cat No: EXWM-4571. | |
| nitronate monooxygenase | Previously classified as 2-nitropropane dioxygenase (EC 1.13.11.32), but it is now recognized that this was the result of the slow ionization of nitroalkanes to their nitronate (anionic) forms. The enzymes from the fungus Neurospora crassa and the yeast Williopsis saturnus var. mrakii (formerly classified as Hansenula mrakII) contain non-covalently bound FMN as the cofactor. Neither hydrogen peroxide nor superoxide were detected during enzyme turnover. Active towards linear alkyl nitronates of lengths between 2 and 6 carbon atoms and, with lower activity, towards propyl-2-nitronate. The enzyme from N. crassa can also utilize neutral nitroalkanes, but with lower activity. Group: Enzymes. Synonyms: NMO; 2-nitropropane dioxygenase (incorrect). Enzyme Commission Number: EC 1.13.12.16. 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-0608; nitronate monooxygenase; EC 1.13.12.16; NMO; 2-nitropropane dioxygenase (incorrect). Cat No: EXWM-0608. | |
| 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(3-butylthiophene-2,5-diyl) | Poly(3-butylthiophene-2,5-diyl) (P3BT) is an alkylthiophene based conducting polymer that can be used as a donor molecule in the development of organic electronics. It is a π-conjugating polymer with a π-π stacking distance of 0.395 nm. Conducting polymer, 80-90% head-to-tail regiospecific conformation. Uses: P3bt can act as a hole transporting layer (htl) which can potentially be used in the fabrication of organic field effect transistors (ofets), chemical sensors, rechargeable batteries and polymeric solar cells (pscs). rechargeable battery electrodes, electrochromic devices, chemical and optical sensors, light-emitting diodes, microelectrical amplifiers, field-effect transistors and non-linear optical materials. Group: 3d printing materials bioelectronic materials organic light-emitting diode (oled) materials. Alternative Names: P3BT. CAS No. 98837-51-5. Pack Sizes: 1 g in glass bottle. Product ID: 3-butyl-2,5-dimethylthiophene. Molecular formula: Mw 54,000 (typical). Mole weight: C10H16S. CCCCC1=C(SC(=C1)C)C. InChI=1S/C10H16S/c1-4-5-6-10-7-8 (2)11-9 (10)3/h7H, 4-6H2, 1-3H3. DUOSBQJOYVIVOR-UHFFFAOYSA-N. | |
| Poly(3-butylthiophene-2,5-diyl) | Poly(3-butylthiophene-2,5-diyl) (P3BT) is an alkylthiophene based conducting polymer that can be used as a donor molecule in the development of organic electronics. It is a π-conjugating polymer with a π-π stacking distance of 0.395 nm. Conducting polymer, 80-90% head-to-tail regiospecific conformation. Uses: P3bt can act as a hole transporting layer (htl) which can potentially be used in the fabrication of organic field effect transistors (ofets), chemical sensors, rechargeable batteries and polymeric solar cells (pscs). rechargeable battery electrodes, electrochromic devices, chemical and optical sensors, light-emitting diodes, microelectrical amplifiers, field-effect transistors and non-linear optical materials. Group: Polymer/macromolecule. Alternative Names: P3BT. CAS No. 98837-51-5. Molecular formula: C10H16S. Mole weight: Mw 54,000 (typical). Appearance: black. IUPACName: 3-butyl-2,5-dimethylthiophene. Canonical SMILES: CCCCC1=C(SC(=C1)C)C. Catalog: ACM98837515-3. | |
| Poly(3-hexylthiophene-2,5-diyl) | Poly(3-hexylthiophene-2,5-diyl) (P3HT) is a poly(alkylthiophene) based semiconducting polymer that is hydrophobic at neutral state and has π-π conjugation in its backbone. It has a hole mobility is in the range of 10-3-10-1 cm2V-1s-1 and is commonly used in the development of field-effect transistors (FETs) for a wide range of applications. Poly(3-hexylthiophene) (P3HT) is a regioregular semiconducting polymer. It is used in organic electronics primarily because of its regular end-to-end arrangement of side chain, which allows efficient p- p stacking of the conjugated backbones. On account of the alkyl side group, P3HT is rendered hydrophobic in neutral state. Solution-to-solid phase transformation and thin film formation of poly(3-hexylthiophene) (P3HT) was reported in a study. Uses: Rechargeable battery electrodes, electrochromic devices, chemical and optical sensors, light-emitting diodes, microelectrical amplifiers, field-effect transistors and non-linear optical materials. for the characterization and solid-state properties of this polymer, see j. am. chem. soc. p3ht, an electron donor that acts as a semiconducting active layer in combination with an electron acceptor li. Group: 3d printing materials bioelectronic materials organic field effect transistor (ofet) materials organic light-emitting diode (oled) materials. Alternative Names: P3HT. CAS No. 156074-98-5. Pack Sizes: 1 g in glass bottle. | |
| Poly(3-hexylthiophene-2,5-diyl) | Poly(3-hexylthiophene-2,5-diyl) (P3HT) is a poly(alkylthiophene) based semiconducting polymer that is hydrophobic at neutral state and has π-π conjugation in its backbone. It has a hole mobility is in the range of 10-3-10-1 cm2V-1s-1 and is commonly used in the development of field-effect transistors (FETs) for a wide range of applications. Poly(3-hexylthiophene) (P3HT) is a regioregular semiconducting polymer. It is used in organic electronics primarily because of its regular end-to-end arrangement of side chain, which allows efficient p- p stacking of the conjugated backbones. On account of the alkyl side group, P3HT is rendered hydrophobic in neutral state. Solution-to-solid phase transformation and thin film formation of poly(3-hexylthiophene) (P3HT) was reported in a study. Uses: Rechargeable battery electrodes, electrochromic devices, chemical and optical sensors, light-emitting diodes, microelectrical amplifiers, field-effect transistors and non-linear optical materials. for the characterization and solid-state properties of this polymer, see j. am. chem. soc. p3ht, an electron donor that acts as a semiconducting active layer in combination with an electron acceptor li. Group: Conductive polymer with enhanced photocatalysis. Alternative Names: P3HT. CAS No. 156074-98-5. Molecular formula: (C10H14S)n. Mole weight: average Mw 50,000-100,000. Appearance: Solid. Catalog: ACM156074985-3. | |
| Polyoxyethylene Alkyl Ethers | Polyoxyethylene alkyl ethers vary considerably in their physical appearance from liquids, to pastes, to solid waxy substances. They are colorless, white, cream-colored or pale yellow materials with a slight odor. CAS No. 9004-95-9. Product ID: PE-0498. Category: Sweetening agent. Product Keywords: Pharmaceutical Excipients; Excipients for Solid Dosage Form; Polyoxyethylene Alkyl Ethers; Sweeteners Excipients; Sweetening agent; /; 9004-95-9; 9004-95-9. UNII: NA. Chemical Name: Polyethylene glycol monocetyl ether; Polyethylene glycol monolauryl ether; Polyethylene glycol monooleyl ether; Polyethylene glycol monostearyl ether. Stability and Storage Conditions: Polyoxyethylene alkyl ethers are chemically stable in strongly acidic or alkaline conditions. The presence of strong electrolytes may, however, adversely affect the physical stability of emulsions containing polyoxyethylene alkyl ethers.On storage, polyoxyethylene alkyl ethers can undergo autoxidation, resulting in the formation of peroxides with an increase in acidity. Many commercially available grades are thus supplied with added antioxidants. Typically, a mixture of 0.01% butylated hydroxyanisole and 0.005% citric acid is used for this purpose. Polyoxyethylene alkyl ethers should be stored in an airtight container, in a cool, dry place. Source and Preparation: Polyoxyethylene alkyl ethers are prepared by the condensation of linear fatty alcohols |  |
| (R)-specific secondary-alkylsulfatase | The enzyme from Rhodococcus ruber is involved in the biodegradation of alkyl sulfate esters used as detergents and released into the environment. The prefered substrates are linear secondary-alkyl sulfate esters, particularly octan-2-yl, octan-3-yl, and octan-4-yl sulfates. The enzyme from Pseudomonas sp. DSM6611 utilizes a range of secondary-alkyl sulfate esters bearing aromatic, olefinic and acetylenic moieties. Perfect enantioselectivities are obtained for substrates bearing groups of different size adjacent to the sulfate moiety. The enzymic hydrolysis proceeds through inversion of the configuration at the stereogenic carbon atom. The enzyme contains a Zn2+ ion. Group: Enzymes. Synonyms: S3 secondary alkylsulphohydrolase; Pisa1; secondary alkylsulphohydrolase; (R)-specific sec-alkylsulfatase; sec-alkylsulfatase. Enzyme Commission Number: EC 3.1.6.19. 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-3752; (R)-specific secondary-alkylsulfatase; EC 3.1.6.19; S3 secondary alkylsulphohydrolase; Pisa1; secondary alkylsulphohydrolase; (R)-specific sec-alkylsulfatase; sec-alkylsulfatase. Cat No: EXWM-3752. | |
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