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| Product | Description | |
|---|---|---|
| trans-7,8,9,10-Tetrahydro-benzo[a]pyrene-7,8-diol Dibenzoate | Used in the preparation of carcinogenic Benzo[a]pyrene Diol Epoxide (B287550). Group: Biochemicals. Grades: Highly Purified. CAS No. 57405-00-2. Pack Sizes: 10mg. US Biological Life Sciences. |  Worldwide |
| 1,1':2',1'':2'',1'''-Quaterphenyl | 1,1':2',1'':2'',1'''-Quaterphenyl is a catalyst for electrochemical reduction of the alkyl chlorides. It is also an intermediate used to prepare Dibenzo[e,l]pyrene (D417375) which is possibly carcinogenic. Group: Biochemicals. Grades: Highly Purified. CAS No. 641-96-3. Pack Sizes: 250mg, 2.5g. Molecular Formula: C24H18, Molecular Weight: 306.399999999999. US Biological Life Sciences. | Worldwide |
| 2, 2'- (1, 4-Naphthalenediyl) bisbenzaldehyde | 2, 2'- (1, 4-Naphthalenediyl) bisbenzaldehyde is an intermediate in the synthesis of Dibenzo[a,i]pyrene (D416985), a polycyclic aromatic hydrocarbon (PAH) with potent carcinogenic activity. Group: Biochemicals. Grades: Highly Purified. CAS No. 285571-20-2. Pack Sizes: 25mg, 100mg. Molecular Formula: C24H16O2. US Biological Life Sciences. | Worldwide |
| Benz[j]aceanthrylene-13C2,d2 and Benz[e]aceanthrylene-13C2,d2 | Labeled Benz[j]aceanthrylene. Polycyclic aromatic hydrocarbons (PAHs) and their PAH-DNA adducts in lung tissues, and their ability to mutate the Ki-ras oncogene in PAH-induced tumors. Seven PAHs were studied: cyclopenta[cd]pyrene (CPP), benzo[a]pyrene (B[a]P), benzo[b]fluoranthene (B[b]F), dibenz[a,h]anthracene (DBA), 5-methylchrysene (5MC), benz[j]aceanthrylene (B[j]A), and dibenzo[a,l]pyrene (DB[a,l]P). Group: Biochemicals. Alternative Names: Benz[7,8]aceanthrylene-13C2,d2 and Benz[4,5]aceanthrylene-13C2,d2. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Benz[j]aceanthrylene and Benz[e]aceanthrylene (70:30 Mixture) | Polycyclic aromatic hydrocarbons (PAHs) and their PAH-DNA adducts in lung tissues, and their ability to mutate the Ki-ras oncogene in PAH-induced tumors. Seven PAHs were studied: cyclopenta[cd]pyrene (CPP), benzo[a]pyrene (B[a]P), benzo[b]fluoranthene (B[b]F), dibenz[a,h]anthracene (DBA), 5-methylchrysene (5MC), benz[j]aceanthrylene (B[j]A), and dibenzo[a,l]pyrene (DB[a,l]P). Group: Biochemicals. Alternative Names: Benz[7,8]aceanthrylene and Benz[4, 5]aceanthrylene. Grades: Highly Purified. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| Dibenzo[a,e]pyrene | Dibenzo[a,e]pyrene. Group: Biochemicals. Alternative Names: 1,2:4,5-Dibenzopyrene; Dibenzo[3, 4:6, 7]pyrene; Dibenzo[a,e]pyrene. Grades: Highly Purified. CAS No. 192-65-4. Pack Sizes: 2.5mg. Molecular Formula: C24H14, Molecular Weight: 302.37. US Biological Life Sciences. | Worldwide |
| Dibenzo[a,e]pyrene-13C6 | Dibenzo[a,e]pyrene-13C6. Group: Biochemicals. Alternative Names: 1,2:4,5-Dibenzopyrene-13C6; Dibenzo[3,4:6,7]pyrene-13C6; Dibenzo[a,e]pyrene-13C6. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C1813C6H14, Molecular Weight: 308.32. US Biological Life Sciences. | Worldwide |
| Dibenzo(a,i)pyrene | Dibenzo(a,i)pyrene is a 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) receptor ligand [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 189-55-9. Pack Sizes: 1 mg; 5 mg. Product ID: HY-124211. |  |
| Dibenzo[a,i]pyrene | Dibenzo[a,i]pyrene is a polycyclic aromatic hydrocarbon (PAH) with potent carcinogenic activity. Dibenzo[a,i]pyrene was shown to induce DNA adduction, tumorigenicity as well as Ki-ras oncogene mutations in strain A/J mouse lung. Dibenzo[a,i]pyrene has been shown to be present in cigarette smoke condensate and in automobile exhaust gas in small quantities. Group: Biochemicals. Alternative Names: Benzo[rst]pentaphene; Benzo[rst]pentacene; 1,2:7,8-Dibenzpyrene; 3,4:9,10-Dibenzopyrene; Dibenzo[b,h]pyrene; NSC 87521. Grades: Highly Purified. CAS No. 189-55-9. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Dibenzo[def,p]chrysene | An active metabolite from inhalation and dermal exposure to polycyclic aromatics hydrocarbons in hot mix asphalt paving workers. DBC is the most potent tumorigen that has been identified to date. Dibenzo[def,p]chrysene (DBC) is a carcinogen and should be handled with appropriate caution. Group: Biochemicals. Alternative Names: 1,2,9,10-Dibenzopyrene; 1,2:3,4-Dibenzopyrene; Dibenzo[a,l]pyrene; 2,3:4,5-Dibenzpyrene; DBC; 4,5,6,7-Dibenzpyrene; Ba 51-090462; NSC 90324. Grades: Highly Purified. CAS No. 191-30-0. Pack Sizes: 1mg, 5mg, 10mg. US Biological Life Sciences. | Worldwide |
| Dibenzo[def,p]chrysene-d14 (Major) | Labelled Dibenzo[a,l]pyrene (D416945). An active metabolite from inhalation and dermal exposure to polycyclic aromatics hydrocarbons in hot mix asphalt paving workers. DBC is the most potent tumorigen that has been identified to date. Group: Biochemicals. Alternative Names: 1,2,9,10-Dibenzopyrene-d14; 1,2:3,4-Dibenzopyrene-d14; Dibenzo[a,l]pyrene-d14; 2,3:4,5-Dibenzpyrene-d14; DBC-d14; 4,5,6,7-Dibenzpyrene-d14; Ba 51-090462-d14; NSC 90324-d14. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| FATPA | Organic Light Emitting Diode (OLED). Alternative Names: 4,4,8,8,12,12-Hexa-p-tolyl-4H-8H-12H-12C-aza-dibenzo[cd,mn]pyrene. CAS No. 1131007-94-7. Molecular formula: C63H51N. Mole weight: 822.09 g/mol. Catalog: ACM1131007947. |  |
| trans-7,8-Dihydroxy-7,8-dihydrobenzo[a]pyrene Dibenzoate | Protected trans-7,8-Dihydroxy-7,8-dihydrobenzo[a]pyrene (D452280), a metabolite of Benzopyrene (B205800). A carcinogen. Group: Biochemicals. Alternative Names: (7R,8R)-rel-7,8-Dihydro-benzo[a]pyrene-7,8-diol 7,8-Dibenzoate. Grades: Highly Purified. CAS No. 57405-08-0. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| unspecific peroxygenase | A heme-thiolate protein (P-450). Enzymes of this type include glycoproteins secreted by agaric basidiomycetes. They catalyse the insertion of an oxygen atom from H2O2 into a wide variety of substrates, including aromatic rings such as naphthalene, toluene, phenanthrene, pyrene and p-nitrophenol, recalcitrant heterocycles such as pyridine, dibenzofuran, various ethers (resulting in O-dealkylation) and alkanes such as propane, hexane and cyclohexane. Reactions catalysed include hydroxylation, epoxidation, N-oxidation, sulfooxidation, O- and N-dealkylation, bromination and one-electron oxidations. They have little or no activity toward chloride. Mechanistically, the catalytic cycle of unspecific (mono)-peroxygenases combines elements of the "shunt" pathway of cytochrome P-450s (a side activity that utilizes a peroxide in place of dioxygen and NAD[P]H) and the classic heme peroxidase cycle. Group: Enzymes. Synonyms: aromatic peroxygenase; mushroom peroxygenase; haloperoxidase-peroxygenase; Agrocybe aegerita peroxidase. Enzyme Commission Number: EC 1.11.2.1. 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-0512; unspecific peroxygenase; EC 1.11.2.1; aromatic peroxygenase; mushroom peroxygenase; haloperoxidase-peroxygenase; Agrocybe aegerita peroxidase. Cat No: EXWM-0512. |  |
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