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25g Pack Size. Group: Building Blocks, Organics. Formula: C6H5NaO4S ¢2H2O. CAS No. 10580-19-5. Prepack ID 30226220-25g. Molecular Weight 232.2. See USA prepack pricing.
Brings about the chlorination of a range of organic molecules, forming stable C-Cl bonds. Also oxidizes bromide and iodide. Enzymes of this type are either heme-thiolate proteins, or contain vanadate. A secreted enzyme produced by the ascomycetous fungus Caldariomyces fumago (Leptoxyphium fumago) is an example of the heme-thiolate type. It catalyses the production of hypochlorous acid by transferring one oxygen atom from H2O2 to chloride. At a separate site it catalyses the chlorination of activated aliphatic and aromatic substrates, via HClO and derived chlorine species. In the absence of halides, it shows peroxidase (e.g. phenol oxidation) and peroxygenase activities. The latter ...peroxidase, and is related to bromide peroxidase (EC 1.11.1.18). It contains vanadate and oxidizes chloride, bromide and iodide into hypohalous acids. In the absence of halides, it peroxygenates organic sulfides and oxidizes ABTS [2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonicacid)] but no phenols. Group: Enzymes. Synonyms: chloroperoxidase; CPO; vanadium haloperoxidase. Enzyme Commission Number: EC 1.11.1.10. CAS No. 9055-20-3. CPO. 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-0491; chloride peroxidase; EC 1.11.1.10; 9055-20-3; chloroperoxidase; CPO; vanadium haloperoxidase. Cat No: EXWM-0491.
peroxidase
Heme proteins with histidine as proximal ligand. The iron in the resting enzyme is Fe(III). They also peroxidize non-phenolic substrates such as 3,3',5,5'-tetramethylbenzidine (TMB) and 2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonicacid) (ABTS). Certain peroxidases (e.g. lactoperoxidase, SBP) oxidize bromide, iodide and thiocyanate. Group: Enzymes. Synonyms: lactoperoxidase; guaiacol peroxidase; plant peroxidase; Japanese radish peroxidase; horseradish peroxidase (HRP); soybean peroxidase (SBP); extensin peroxidase; heme peroxidase; oxyperoxidase; protoheme peroxidase; pyrocatechol peroxidase; scopoletin peroxidase; Coprinus cinereus peroxidase; Arthromyces ramosus peroxidase. Enzyme Commission Number: EC 1.11.1.7. CAS No. 9003-99-0. Peroxidase. 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-0509; peroxidase; EC 1.11.1.7; 9003-99-0; lactoperoxidase; guaiacol peroxidase; plant peroxidase; Japanese radish peroxidase; horseradish peroxidase (HRP); soybean peroxidase (SBP); extensin peroxidase; heme peroxidase; oxyperoxidase; protoheme peroxidase; pyrocatechol peroxidase; scopoletin peroxidase; Coprinus cinereus peroxidase; Arthromyces ramosus peroxidase. Cat No: EXWM-0509.
Effective ligand for the Pd-catalyzed arylation of pyrazoles, indazoles and amino heterocycles. Ligand used in the Pd-catalyzed synthesis of phenols from aryl halides and KOH. Ligand used in the Pd-catalyzed of benzoic acids from aryl halides and CO2. Ligand used in the Pd-catalyzed trifluoromethylation of vinyl sulfonates. Ligand used in the Pd-catalyzed arylation of nitroacetates. Ligand used in the Pd-catalyzed Suzuki-Miyaura cross-coupling of allylboronates and aryl halides. Ligand used in the Pd-catalyzed cyanation of (hetero)arylchlorides and bromides. Ligand used in the Pd-catalyzed C-N cross coupling of sulfinamides and aryl halides. Ligand used in the Pd-catalyzed arylation of cyanamides. Group: Organic phosphine compounds. Alternative Names: DTXSID70469549; t-Bu XPhos; FT-0689983; TC-121258; 2-Di-tert-butylphosphino-2 inverted exclamation marka,4 inverted exclamation marka,6 inverted exclamation marka-triisopropylbiphenyl; tBuXPhos; ditert-butyl-[2-(2,4,6-triisopropylphenyl)phenyl]phosphane; ZINC56961724; 2-Di-tert-butylphosphino-2',4',6'-triisopropylbiphenyl; 2-(di-tert-butylphosphino)-2', 4',6'-triisopropylbiphenyl. CAS No. 564483-19-8. Molecular formula: C29H45P. Mole weight: 424.653g/mol. IUPACName: ditert-butyl-[2-[2,4,6-tri(propan-2-yl)phenyl]phenyl]phosphane. Canonical SMILES: CC (C)C1=CC (=C (C (=C1)C (C)C)C2=CC=CC=C2P (C (C) (C)C)C (C) (C)C)C (C)C. Catalog: ACM5644
A reactant used in the preparation of the immunosuppressive agent FTY720 (F805000). Group: Biochemicals. Alternative Names: 1,1,1-Trifluoro-methanesulfonicAcid 4-[2- (Acetyloxy) ethyl]phenyl Ester. Grades: Highly Purified. CAS No. 712223-57-9. Pack Sizes: 50mg. US Biological Life Sciences.
Worldwide
Fensulfothion Oxon Sulfone
Fensulfothion Oxon Sulfone. Group: Biochemicals. Alternative Names: Diethyl 4-(Methylsulfonyl)phenyl Ester Phosphoric Acid; p-(Methylsulfonyl)-phenol Diethyl Phosphate; Diethyl 4-Methylsulfonylphenyl Phosphate; Fensulfothion Oxon Sulfone; Fensulfothion Oxygen Analog Sulfone; O,O-Diethyl O-(4-Methylsulfonylphenyl) Phosphate. Grades: Highly Purified. CAS No. 6132-17-8. Pack Sizes: 100mg. Molecular Formula: C11H17O6PS, Molecular Weight: 308.29. US Biological Life Sciences.
Hydrobromic acid is a strong acid that is used in conjunction with Phenol (P318005) to carry out rapid cleavage of sulfonamides. Hydrobromic acid is primarily used in chemistry to produce inorganic bromides, and is also used in isomerization reactions. Group: Biochemicals. Grades: Highly Purified. CAS No. 10035-10-6. Pack Sizes: 100ml, 250ml. Molecular Formula: HBr. US Biological Life Sciences.
Worldwide
Hydrobromic Acid-d Solution (47 wt. % in D2O)
Hydrobromic Acid-d, is the labeled analogue of Hydrobromic Acid (H714585), a strong acid that is used in conjunction with Phenol (P318005) to carry out rapid cleavage of sulfonamides. Hydrobromic acid is primarily used in chemistry to produce inorganic bromides, and is also used in isomerization reactions. Group: Biochemicals. Grades: Highly Purified. CAS No. 13536-59-9. Pack Sizes: 1g, 2.5g. Molecular Formula: DBr, Molecular Weight: 81.92. US Biological Life Sciences.
Worldwide
Hydrobromic Acid Solution (in Acetic Acid)
Hydrobromic acid is a strong acid that is used in conjunction with Phenol (P318005) to carry out rapid cleavage of sulfonamides. Hydrobromic acid is also used as a catalyst to reduce sulfoxides, such as Dimethyl sulfoxide (D479380). Group: Biochemicals. Grades: Highly Purified. CAS No. 37348-16-6. Pack Sizes: 10ml, 25ml. Molecular Formula: HBr. US Biological Life Sciences.
Worldwide
Methiocarb-d3 Sulfone
Methiocarb-d3 Sulfone. Group: Biochemicals. Alternative Names: Methylcarbamic Acid 4-(Methylsulfonyl)-3,5-xylyl Ester-d3; 3,5-Dimethyl-4-(methylsulfonyl)phenol Methylcarbamate-d3; 4-(Methylsulfonyl)-3,5-xylenol Methylcarbamate-d3; BAY 41790-d3; Ba 51-084786-d3; Bay 37344 Sulfone-d3; Bayer 37344 Sulfone-d3; Mesurol Sulfone-d3. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C11H12D3NO4S, Molecular Weight: 260.32. US Biological Life Sciences.
Worldwide
Methiocarb Sulfone
Methiocarb Sulfone. Group: Biochemicals. Alternative Names: Methylcarbamic Acid 4-(Methylsulfonyl)-3,5-xylyl Ester; 3,5-Dimethyl-4-(methylsulfonyl)phenol Methylcarbamate; 4-(Methylsulfonyl)-3,5-xylenol Methylcarbamate; BAY 41790; Ba 51-084786; Bay 37344 sulfone; Bayer 37344 Sulfone; Mesurol Sulfone. Grades: Highly Purified. CAS No. 2179-25-1. Pack Sizes: 250mg. Molecular Formula: C11H15NO4S, Molecular Weight: 257.31. US Biological Life Sciences.
Catalyst used for the selective hydration of substituted alkynes at room temperature without acidic promoters. Gold(I) catalyzes bromination of terminal alkynes. Sequential O-H/C-H bond insertion of phenols initiated by the gold(I)-catalyzed cyclization of 1-bromo-1,5-enynes. Ligand-controlled gold-catalyzed cycloisomerization of 1,n-enyne esters toward synthesis of dihydronaphthalene. Group: Gold catalysts. Alternative Names: MFCD21363047; Tri-t-butylphosphine[bis (trifluoromethyl)sulfonylimido]gold (I); 1121960-93-7. CAS No. 1121960-93-7. Molecular formula: C14H28AuF6NO4PS2+. Mole weight: 680.432g/mol. IUPACName: bis(trifluoromethylsulfonyl)azanide; gold(1+); tritert-butylphosphanium. Canonical SMILES: CC (C) (C)[PH+] (C (C) (C)C)C (C) (C)C. C (F) (F) (F)S (=O) (=O)[N-]S (=O) (=O)C (F) (F)F. [Au+]. Catalog: ACM1121960937.
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