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Has a mutagenic potency. Group: Biochemicals. Alternative Names: [1,1-Biphenyl]-2-amine; 2-Biphenylamine; 2-Aminodiphenyl; 2-Phenylaniline; 2-Phenylbenzenamine; o-Aminobiphenyl. Grades: Highly Purified. CAS No. 90-41-5. Pack Sizes: 1g. US Biological Life Sciences.
Worldwide
2-Aminobiphenyl-2,3,4,5,6-d5
2-Aminobiphenyl-2,3,4,5,6-d5. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences.
Catacxium a-pd-g2,chloro[(di(1-adamantyl)-N-butylphosphine)-2-(2-aminobiphenyl)]palladium(II). Uses: Designed for use in research and industrial production. Product Category: Organic Phosphine Compounds. Appearance: Brown powder. CAS No. 1375477-29-4. Molecular formula: C36H49ClNPPd. Mole weight: 668.63. Purity: 0.98. Product ID: ACM1375477294. Alfa Chemistry ISO 9001:2015 Certified.
Chloro[(1,3,5,7-tetramethyl-5-phenyl-2,4,8-trioxa-6-phosphaadamantane)-2-(2-aminobiphenyl)]palladium(II). Uses: Designed for use in research and industrial production. Product Category: Amines. CAS No. 1350851-22-7. Mole weight: 602.4. Product ID: ACM1350851227. Alfa Chemistry ISO 9001:2015 Certified.
Chloro[ (tri-tert-butylphosphine) -2- (2-aminobiphenyl) ]palladium (II)
Chloro[ (tri-tert-butylphosphine) -2- (2-aminobiphenyl) ]palladium (II) . Group: Biochemicals. Grades: Highly Purified. CAS No. 1375325-71-5. Pack Sizes: 250mg, 500mg, 1g, 2g, 5g. US Biological Life Sciences.
Chloro[(tri-tert-butylphosphine)-2-(2-aminobiphenyl)]palladium(II). Uses: Catalyst for the suzuki coupling of brominated 2,1-borazaronaphthalenes and potassium organotrifluoroborates. Additional or Alternative Names: Chloro[(tri-tert-butylphosphine)-2-(2-aminobiphenyl)] palladium(II). Product Category: Palladium series catalysts. Appearance: off-white to pale yellow powder. CAS No. 1375325-71-5. Molecular formula: C24H37ClNPPd. Mole weight: 512.41. Purity: 0.98. Product ID: ACM1375325715. Alfa Chemistry ISO 9001:2015 Certified.
2-Aminodiphenyl-d9. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2-AMINODIPHENYL-D9;2-AMINOBIPHENYL-D9. Product Category: Heterocyclic Organic Compound. CAS No. 344298-97-1. Molecular formula: C12H2D9N. Mole weight: 178.28. Purity: 98 atom % D. IUPACName: 2,3,4,5-tetradeuterio-6-(2,3,4,5,6-pentadeuteriophenyl)aniline. Canonical SMILES: C1=CC=C(C=C1)C2=CC=CC=C2N. Product ID: ACM344298971. Alfa Chemistry ISO 9001:2015 Certified.
2'-Aminobiphenyl-3-carboxylic Acid Hydrochloride
2'-Aminobiphenyl-3-carboxylic Acid Hydrochloride. Group: Biochemicals. Grades: Highly Purified. CAS No. 1172351-47-1. Pack Sizes: 25mg, 50mg. Molecular Formula: C13H11NO2; HCl, Molecular Weight: 213.233645999999. US Biological Life Sciences.
Worldwide
biphenyl-2,3-diol 1,2-dioxygenase
Contains Fe2+ or Mn2+. This enzyme participates in the degradation pathway of biphenyl and PCB (poly chlorinated biphenyls), and catalyses the first ring cleavage step by incorporating two oxygen atoms into the catechol ring formed by EC 1.3.1.56, cis-2,3-dihydrobiphenyl-2,3-diol dehydrogenase.The enzyme from the bacterium Burkholderia xenovorans LB400 can also process catechol, 3-methylcatechol, and 4-methylcatechol, but less efficiently. The enzyme from the carbazole-degrader Pseudomonas resinovorans strain CA10 also accepts 2'-aminobiphenyl-2,3-diol. The enzyme from Ralstonia sp. SBUG 290 can also accept 1,2-dihydroxydibenzofuran and 1,2-dihydroxynaphthalene. The enzyme is strongly inhibited by the substrate.Not identical with EC 1.13.11.2 catechol 2,3-dioxygenase. Group: Enzymes. Synonyms: 2,3-dihydroxybiphenyl dioxygenase; biphenyl-2,3-diol dioxygenase; bphC (gene name); biphenyl-2,3-diol:oxygen 1,2-oxidoreductase (decyc. Enzyme Commission Number: EC 1.13.11.39. CAS No. 103679-58-9. 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-0558; biphenyl-2,3-diol 1,2-dioxygenase; EC 1.13.11.39; 103679-58-9; 2,3-dihydroxybiphenyl dioxygenase; biphenyl-2,3-diol dioxygenase; bphC (gene name); biphenyl-2,3-diol:oxygen 1,2-oxidoreductase (decyclizing). Cat No: EXWM-0558.
carbazole 1,9a-dioxygenase
This enzyme catalyses the first reaction in the pathway of carbazole degradation. The enzyme attacks at the 1 and 9a positions of carbazole, resulting in the formation of a highly unstable hemiaminal intermediate that undergoes a spontaneous cleavage and rearomatization, resulting in 2'-aminobiphenyl-2,3-diol. In most bacteria the enzyme is a complex composed of a terminal oxygenase, a ferredoxin, and a ferredoxin reductase. The terminal oxygenase component contains a nonheme iron centre and a Rieske [2Fe-2S] iron-sulfur cluster. Group: Enzymes. Synonyms: CARDO. Enzyme Commission Number: EC 1.14.12.22. 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-0689; carbazole 1,9a-dioxygenase; EC 1.14.12.22; CARDO. Cat No: EXWM-0689.
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