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| Product | Description | |
|---|---|---|
| Pentachlorophenol | Used as insecticide for terminate control; pre-harvest defoliant; general herbicide. Antimicrobial preservative and fungicide for wood, wood products, starches, textiles, paints, adhesives, leather, pulp, paper, industrial waste systems, building materials. Surface disinfectant. Group: Biochemicals. Alternative Names: 1-Hydroxy-2,3,4,5,6-pentachlorobenzene; 1-Hydroxypentachloro Benzene ; 2,3,4,5,6-Pentachlorophenol; Chlon; Chlorophenasic Acid; Dowicide 7; Dowicide EC 7; Dura Treet II; EP 30; EP 30 (pesticide); Fungifen; Grundier Arbezol; Lauxtol; Liroprem; NSC 263497; PCP; PCP (pesticide); PKhF; Penchlorol; Penta; Penton 70; Pentor 70; Perchlorophenol; Permasan; Pol Nu; Preventol P; Santophen 20; Satophen; Witophen P; Woodtreat A. Grades: Highly Purified. CAS No. 87-86-5. Pack Sizes: 100mg. US Biological Life Sciences. |  Worldwide |
| pentachlorophenol monooxygenase | A flavoprotein (FAD). The enzyme displaces a diverse range of substituents from the 4-position of polyhalogenated phenols but requires that a halogen substituent be present at the 2-position. The enzyme converts many polyhalogenated phenols into hydroquinones, and requires that a halogen substituent be present at C-2. If C-4 carries a halogen substituent, reaction 1 is catalysed, e.g. 2,4,6-triiodophenol is oxidized to 2,6-diiodohydroquinone; if C-4 is unsubstituted, reaction 2 is catalysed. Group: Enzymes. Synonyms: pentachlorophenol dechlorinase; pentachlorophenol dehalogenase; pentachlorophenol 4-monooxygenase; PCP hydroxylase; pentachlorophenol hydroxylase; PcpB; PCB 4-monooxygenase; PCB4MO. Enzyme Commission Number: EC 1.14.13.50. CAS No. 136111-57-4. 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-0857; pentachlorophenol monooxygenase; EC 1.14.13.50; 136111-57-4; pentachlorophenol dechlorinase; pentachlorophenol dehalogenase; pentachlorophenol 4-monooxygenase; PCP hydroxylase; pentachlorophenol hydroxylase; PcpB; PCB 4-monooxygenase; PCB4MO. Cat No: EXWM-0857. |  |
| Pentachlorophenol,sodium salt | Heterocyclic Organic Compound. CAS No. 123333-54-0. Molecular formula: C6Cl5O. Catalog: ACM123333540. |  |
| 2,4,5,6-Tetrachlorophenol (contains 10% pentachlorophenol) | Used as a broad range pesticide against insects, fungi, vegetation and bacteria. It has become a common environmental contaminant and probable human carcinogen. Group: Biochemicals. Alternative Names: 2,3,4,6-Tetrachloro-phenol; 2,3,4,6-Tetrachlorophenate; Dowicide 6; NSC 2428. Grades: Highly Purified. CAS No. 58-90-2. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| N, N'-Dicyclohexyl carbodiimide Pentachlorophenol Complex (Kovacs Complex) | Useful reagent for preparing amino acid pentachlorophenol active esters. Group: Biochemicals. Alternative Names: Kovacs Complex. Grades: Highly Purified. Pack Sizes: 10g. US Biological Life Sciences. | Worldwide |
| 2,3-Dichloroanisole | 2,3-Dichloroanisole is a metabolite of pentachlorophenol with fungicidal activity. 2,3-Dichloroanisole aling with other found in marine sediments. Group: Biochemicals. Alternative Names: 1,2-Dichloro-3-methoxybenzene; 2,3-Dichlorophenyl Methyl Etherl. Grades: Highly Purified. CAS No. 1984-59-4. Pack Sizes: 25g. US Biological Life Sciences. | Worldwide |
| Chloranil | Chloranil (Tetrachloro-p-benzoquinone), an orally active metabolite of pentachlorophenol and hexachlorobenzene, is a widely used fungicide. Chloranil can induce ROS production. Chloranil induces neutrophil extracellular traps through the ROS-JNK-NOX2 pathway. Chloranil induces ferroptosis and neuroinflammation. Chloranil induces apoptosis of mouse embryonic stem cells [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Tetrachloro-p-benzoquinone; TCBQ. CAS No. 118-75-2. Pack Sizes: 10 mM * 1 mL; 25 g; 100 g. Product ID: HY-Y0278. |  |
| Tetrachloro-1,4-benzoquinone | Tetrachloro-1,4-benzoquinone is a potential intermediate in the process of pentachlorophenol-induced carcinogenicity. Group: Biochemicals. Grades: Highly Purified. CAS No. 118-75-2. Pack Sizes: 5g, 25g, 100g. Molecular Formula: C?Cl?O?, Molecular Weight: 245.88. US Biological Life Sciences. | Worldwide |
| Tetrachlorocatechol | Tetrachlorocatechol is a metabolite of pentachlorophenol. Tetrachlorocatechol is one of the most toxic chlorinated catechol produced by the chlorobleaching of pulp and frequently found in the kraft pulp mill effluents [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1198-55-6. Pack Sizes: 10 mM * 1 mL; 500 mg. Product ID: HY-W006000. | |
| Tetrachlorohydroquinone | Tetrachlorohydroquinone (TCHQ) is a metabolite of pentachlorophenol. Tetrachlorohydroquinone increases DNA lesions and induce oxidative stress in rodents [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: TCHQ; Tetrachloroquinol. CAS No. 87-87-6. Pack Sizes: 10 mM * 1 mL; 1 g. Product ID: HY-W144308. | |
| Tetrachloro-p-benzoquinone | Tetrachloro-1,4-benzoquinone is a potential intermediate in the process of pentachlorophenol-induced carcinogenicity. Fluorescence quencher; oxidizing agent; aromatizing reagent. Group: Biochemicals. Grades: Highly Purified. CAS No. 118-75-2. Pack Sizes: 250g, 500g, 1kg, 2kg. Molecular Formula: C?Cl?O?, Molecular Weight: 245.87. US Biological Life Sciences. | Worldwide |
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