A directory of where to buy chemicals in the USA, including: distributors, industrial manufacturers, bulk supplies and wholesalers of raw ingredients & finished goods.
Atomic number of base material: 51 Antimony. Uses: Stibonium salts, cocatalyst in converting trienes to aromatics and hydroaromatics, react with nitricsulfuric acid to give trinitro derivatives, polymerization inhibitor, lubricating-oil additive. Group: Micro/nanoelectronics. Alternative Names: Antimony(III)triphenyl, Triphenylstibine. CAS No. 603-36-1. Molecular formula: (C6H5)3Sb. Mole weight: 353.07. IUPACName: triphenylstibane. Canonical SMILES: c1ccc(cc1)[Sb](c2ccccc2)c3ccccc3. ECNumber: 210-037-6. Catalog: ACM603361.
Triphenylantimony(III)
Atomic number of base material: 51 Antimony. Uses: Stibonium salts, cocatalyst in converting trienes to aromatics and hydroaromatics, react with nitricsulfuric acid to give trinitro derivatives, polymerization inhibitor, lubricating-oil additive. Group: Vapor deposition precursors. Alternative Names: Antimony(III)triphenyl, Triphenylstibine. CAS No. 603-36-1. Pack Sizes: 25, 100 g in glass bottle. Product ID: triphenylstibane. Molecular formula: 353.07. Mole weight: (C6H5)3Sb. c1ccc(cc1)[Sb](c2ccccc2)c3ccccc3. 1S/3C6H5.Sb/c3*1-2-4-6-5-3-1; /h3*1-5H; , HVYVMSPIJIWUNA-UHFFFAOYSA-N. HVYVMSPIJIWUNA-UHFFFAOYSA-N.
Triphenylarsine
Triphenylarsine. Group: Biochemicals. Grades: Highly Purified. CAS No. 603-32-7. Pack Sizes: 5g, 10g, 25g, 50g, 100g. US Biological Life Sciences.
5g Pack Size. Group: Phenols, Reagents, Research Organics & Inorganics. Formula: C18H15Bi. CAS No. 603-33-8. Prepack ID 54224853-5g. Molecular Weight 440.3. See USA prepack pricing.
Triphenylbismuth Carbonate
Triphenylbismuth Carbonate. Group: Biochemicals. Alternative Names: [Carbonato(2-)-O]triphenylbismuth. Grades: Highly Purified. CAS No. 47252-14-2. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. US Biological Life Sciences.
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Triphenylbismuth Diacetate
Triphenylbismuth Diacetate. Group: Biochemicals. Alternative Names: Bis(acetato-O)triphenylbismuth. Grades: Highly Purified. CAS No. 7239-60-3. Pack Sizes: 1g, 2g, 5g, 10g, 25g. US Biological Life Sciences.
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Triphenylbismuth Dichloride
Triphenylbismuth Dichloride. Group: Biochemicals. Alternative Names: Dichlorotri phenylbismuth. Grades: Highly Purified. CAS No. 594-30-9. Pack Sizes: 1g, 2g, 5g, 10g, 25g. US Biological Life Sciences.
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Triphenylbismuth Difluoride
Triphenylbismuth Difluoride. Group: Biochemicals. Alternative Names: Difluorotri phenylbismuth. Grades: Highly Purified. CAS No. 2023-48-5. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. US Biological Life Sciences.
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Triphenylborane
Triphenylborane is generally immediately available in most volumes. Uses: Triphenylborane powder is a boron based precursor that can be used in the chemical vapor deposition for the development of carbon nanomaterials for application in oxygen reduction reaction, hydrogen storage, transparent conducting films, and fluoride shuffle batteries. Group: Vapor deposition precursors. Alternative Names: Triphenylboron; Triphenylborine; Borane,triphenyl-. CAS No. 960-71-4. Pack Sizes: 2.5, 10 g in glass bottle. Product ID: triphenylborane. Molecular formula: 242.13. Mole weight: (C6H5)3B. c1ccc(cc1)B(c2ccccc2)c3ccccc3. InChI=1S/C18H15B/c1-4-10-16 (11-5-1) 19 (17-12-6-2-7-13-17) 18-14-8-3-9-15-18/h1-15H. MXSVLWZRHLXFKH-UHFFFAOYSA-N. 99% | 99.9% | 99.99% | 99.999%.
Triphenylborane
Triphenylborane is generally immediately available in most volumes. Uses: Triphenylborane powder is a boron based precursor that can be used in the chemical vapor deposition for the development of carbon nanomaterials for application in oxygen reduction reaction, hydrogen storage, transparent conducting films, and fluoride shuffle batteries. Group: Other. Alternative Names: Triphenylboron; Triphenylborine; Borane, triphenyl-. CAS No. 960-71-4. Molecular formula: (C6H5)3B. Mole weight: 242.13. Appearance: Crystalline powder. Purity: 99% | 99.9% | 99.99% | 99.999%. IUPACName: triphenylborane. Canonical SMILES: c1ccc(cc1)B(c2ccccc2)c3ccccc3. Density: 0.898 g/mL at 25 °C. ECNumber: 213-504-2. Catalog: ACM960714.
An organoborane compound with chemosterilant activity against Cochliomyia hominivorax (screwworm flies). A competitive inhibitor of urease of Klebsiella aerogenes used to study the mechanisms of interaction with the nickel active site. Group: Biochemicals. Alternative Names: Boric Acid Triphenyl Ester; Phenyl Borate; Boron Triphenoxide; NSC 806; Triphenoxyborane; Triphenoxyboron. Grades: Highly Purified. CAS No. 1095-03-0. Pack Sizes: 10g. US Biological Life Sciences.
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Triphenylchlorosilane
Triphenylchlorosilane. Group: Biochemicals. Alternative Names: Chlorotriphenylsilane; Triphenylsilyl Chloride. Grades: Highly Purified. CAS No. 76-86-8. Pack Sizes: 25g, 50g, 100g, 250g, 500g. US Biological Life Sciences.
Triphenylgermanium hydride is a hydrogen donor. Uses: It may be used in the isomerization of (z) alkene.1 tempo (2,2,6,6-tetramethylpiperidinyloxy) reacts with triphenylgermanium hydride to form its corresponding germyl radical. 2. Group: Saltvapor deposition precursors. Alternative Names: Triphenylgermane,Triphenylgermanyl hydride. CAS No. 2816-43-5. Pack Sizes: 5 g in glass bottle. Molecular formula: 304.96. Mole weight: (C6H5)3GeH. c1ccc(cc1)[GeH](c2ccccc2)c3ccccc3. 1S/C18H16Ge/c1-4-10-16 (11-5-1) 19 (17-12-6-2-7-13-17) 18-14-8-3-9-15-18/h1-15, 19H, NXHORDQDUDIXOS-UHFFFAOYSA-N. NXHORDQDUDIXOS-UHFFFAOYSA-N.
Triphenylmethane. Group: Biochemicals. Grades: Highly Purified. CAS No. 519-73-3. Pack Sizes: 100g, 250g, 500g, 1kg, 2kg. Molecular Formula: C19H16. US Biological Life Sciences.
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Triphenylmethane sulfenyl Chloride
Intermediate in the preparation of precursors for cyclic polysulfides. Group: Biochemicals. Alternative Names: Tritylsulfenyl Chloride; NSC 378986; Triphenylmethane sulfanyl Chloride; α,α-Diphenyl-benzenemethanesulfenyl Chloride. Grades: Highly Purified. CAS No. 24165-03-5. Pack Sizes: 2.5g. US Biological Life Sciences.
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Triphenylmethanol
A triaryl methane derivative as antiproliferative agent. Group: Biochemicals. Grades: Highly Purified. CAS No. 76-84-6. Pack Sizes: 1g, 10g, 50g, 100g. Molecular Formula: C??H??O. US Biological Life Sciences.
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Triphenylmethanol
Triphenylmethanol (Zidovudine EP Impurity D) is a triaryl methane derivative as antiproliferative agent. Synonyms: triphenylmethanol. Grades: ≥ 99 % (HPLC). CAS No. 76-84-6. Molecular formula: C19H16O. Mole weight: 260.33.
Triphenylmethanol, 98.0 % +(HPLC)
Triphenylmethanol, 98.0 % +(HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 100g, 250g, 1Kg, 5Kg. US Biological Life Sciences.
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Triphenylmethylamine
Triphenylmethylamine is structurally related to Clotrimazole, which is an antifungal medication commonly used in the treatment of fungal infections. Synonyms: α,α-Diphenylbenzenemethanamine; Tritylamine; Aminotriphenylmethane; NSC 1154; Triphenylmethanamine. Grades: ≥95%. CAS No. 5824-40-8. Molecular formula: C19H17N. Mole weight: 259.34.
Triphenylmethylamine
Triphenylmethylamine is a trityl derivative that is structurally related to Clotrimazole. Triphenylmethylamine is used in the preparation of trityl-cysteine analogs as inhibitors of human mitotic kinesin. Triphenylmethylamine is also used as a fireproofing agent. Group: Biochemicals. Alternative Names: α , α -Diphenyl Benzene methanamine; Tritylamine; Aminotriphenylmethane; NSC 1154; Triphenylmethanamine. Grades: Highly Purified. CAS No. 5824-40-8. Pack Sizes: 25g. US Biological Life Sciences.
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Triphenylmethyl chloride
Triphenylmethyl chloride. CAS No. 76-83-5.
Pennsylvania PA
Triphenylmethyl chloride 99+% (HPLC)
Triphenylmethyl chloride 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. CAS No. 76-83-5. Pack Sizes: 100g, 250g, 1Kg, 5Kg, 10Kg. US Biological Life Sciences.
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Triphenylmethylium Tetrafluoroborate
Triphenylmethylium Tetrafluoroborate. Group: Biochemicals. Alternative Names: Triphenylcarbenium Tetrafluoroborate; Tritylium Tetrafluoroborate. Grades: Highly Purified. CAS No. 341-02-6. Pack Sizes: 5g, 10g, 25g, 50g, 100g. US Biological Life Sciences.
Triphenyl phosphate (TPhP) is the chemical compound with the formula OP(OC6H5)3. This colourless solid is the ester (triester) of phosphoric acid and phenol. It is used as a plasticizer and a fire retardant in a wide variety of settings and products. Group: Battery materials plastic additivesplasticizers. Alternative Names: Phosphoric acid, triphenyl ester. CAS No. 115-86-6. Product ID: Triphenyl phosphate. Molecular formula: 326.28. Mole weight: C18H15O4P. C1=CC=C (C=C1)OP (=O) (OC2=CC=CC=C2)OC3=CC=CC=C3. XZZNDPSIHUTMOC-UHFFFAOYSA-N. InChI=1S/C18H15O4P/c19-23 (20-16-10-4-1-5-11-16, 21-17-12-6-2-7-13-17) 22-18-14-8-3-9-15-18/h1-15H. >99.0%(GC).
Triphenyl phosphate is an organic phosphate flame retardant. Triphenyl phosphate can disrupt placental tryptophan metabolism by activating MAOA/ROS/NFκB , leading to abnormal neurological behavior. Triphenyl phosphate promotes oxidative stress by inducing inflammatory factors like nuclear factor kappa B ( NFκB ), interleukin-6 , and tumor necrosis factor &alpha. Triphenyl phosphate can also cause allergic contact dermatitis [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 115-86-6. Pack Sizes: 10 mM * 1 mL; 100 g; 500 g. Product ID: HY-Y1322.
Triphenyl phosphate
Triphenyl phosphate. Group: Biochemicals. Grades: Highly Purified. CAS No. 115-86-6. Pack Sizes: 250g, 500g, 1kg, 2kg, 5kg. Molecular Formula: C18H15O4P. US Biological Life Sciences.
Worldwide
Triphenyl Phosphate
Triphenyl Phosphate. We stock inventory in warehouses throughout the United States, allowing us to serve customers in all regions in a timely and cost effective manner.
California
Triphenyl Phosphate
Triphenyl phosphate appears as colorless crystals. (NTP, 1992);Liquid; PelletsLargeCrystals; PelletsLargeCrystals, Liquid;COLOURLESS CRYSTALLINE POWDER WITH CHARACTERISTIC ODOUR.;Colorless, crystalline powder with a phenol-like odor.;Colorless, crystalline powder with a phenol-like odor. Group: Polymers. Product ID: triphenyl phosphate. Molecular formula: 326.3g/mol. Mole weight: (C6H5)3PO4;C18H15O4P;C18H15O4P. C1=CC=C (C=C1)OP (=O) (OC2=CC=CC=C2)OC3=CC=CC=C3. InChI=1S/C18H15O4P/c19-23 (20-16-10-4-1-5-11-16, 21-17-12-6-2-7-13-17) 22-18-14-8-3-9-15-18/h1-15H. XZZNDPSIHUTMOC-UHFFFAOYSA-N.
Triphenyl Phosphate-13C6
Triphenyl Phosphate-13C6 is an isotope labelled compound of Triphenyl phosphate (T808990). Triphenyl Phosphate is used in the insecticidal composition. Also acts as a flame retardant. Triphenyl phosphate is also added to some nail polishes as a replacement for the plasticizer dibutyl phthalate (D429495). Diphenyl phosphate (D492000), metabolite of triphenyl phosphate increased sharply in the urine of women 10-14 hours after they painted their nails with polish containing triphenyl phosphate. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 2mg, 5mg. Molecular Formula: C1813C6H15O4P, Molecular Weight: 404.3. US Biological Life Sciences.
Isotope labelled Triphenyl Phosphate (T808990) is an insecticidal composition and also acts as a flame retardant. Group: Biochemicals. Alternative Names: Phosphoric Acid Triphenyl Ester-d15 Celluflex TPP-d15; Disflamoll TP-d15; NSC 57868-d15; Phenyl Phosphate-d15; Phoscon FR 903N-d15; Phosflex TPP-d15; Reofos TPP-d15; S 4-d15; Sumilizer TPP-d15; TP-d15 TPP-d15; TPPA-d15; TTP-d15; Triphenoxyphosphine Oxide-d15; Wako TPP-d15. Grades: Highly Purified. CAS No. 1173020-30-8. Pack Sizes: 2.5mg. US Biological Life Sciences.
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Triphenyl Phosphate, Reagent
Triphenyl phosphate appears as colorless crystals. (NTP, 1992);Liquid; PelletsLargeCrystals; PelletsLargeCrystals, Liquid;COLOURLESS CRYSTALLINE POWDER WITH CHARACTERISTIC ODOUR.;Colorless, crystalline powder with a phenol-like odor.;Colorless, crystalline powder with a phenol-like odor. Group: Plasticizers. CAS No. 115-86-6. Product ID: triphenyl phosphate. Molecular formula: 326.3g/mol. Mole weight: (C6H5)3PO4;C18H15O4P;C18H15O4P. C1=CC=C (C=C1)OP (=O) (OC2=CC=CC=C2)OC3=CC=CC=C3. InChI=1S/C18H15O4P/c19-23 (20-16-10-4-1-5-11-16, 21-17-12-6-2-7-13-17) 22-18-14-8-3-9-15-18/h1-15H. XZZNDPSIHUTMOC-UHFFFAOYSA-N.
Triphenylphosphine
Triphenylphosphine is a member of the class of tertiary phosphines that is phosphane in which the three hydrogens are replaced by phenyl groups. It has a role as a reducing agent. It is a member of benzenes and a tertiary phosphine. CAS No. 603-35-0. Product ID: PE-0666. Molecular formula: C18H15P. Category: Synthetic catalyst. Product Keywords: Catalysts; Triphenylphosphine; PE-0666; Synthetic catalyst; C18H15P; 603-35-0. Color: White. EC Number: 210-036-0. Physical State: Crystals, Crystalline Powder or Flakes. Solubility: water: soluble0.00017 g/L at 22°C. Storage: Store below +30°C. Applications: Triphenylphosphine is used as a polymerization initiator and an intermediate to make pharmaceuticals, phosphonium salts, and other phosphorus compounds. Boiling Point: 377 °C(lit.). Melting Point: 79-81 °C(lit.). Density: 1.132. Product Description: Triphenylphosphine is used as a polymerization initiator and an intermediate to make pharmaceuticals, phosphonium salts, and other phosphorus compounds.
Triphenylphosphine 99.5+% (GC). Group: Biochemicals. Grades: GC. Pack Sizes: 25g, 100g, 250g, 1Kg, 5Kg. US Biological Life Sciences.
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Triphenylphosphine Borane
Triphenylphosphine Borane. Group: Biochemicals. Alternative Names: Borane - Triphenylphosphine Complex. Grades: Highly Purified. CAS No. 2049-55-0. Pack Sizes: 10g, 25g, 50g, 100g, 250g. US Biological Life Sciences.
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Triphenylphosphinechlorogold
Triphenylphosphinechlorogold is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: Chloro(triphenylphosphine)gold(I). CAS No. 14243-64-2. Pack Sizes: 100 mg; 250 mg. Product ID: HY-W020955.
Triphenylphosphinegold(I) bis (trifluoromethanesulfonyl)imidate, min. 98%
Catalyst promoting the addition of nucleophiles to alleneamides. Gold- and Bronsted acid-catalyzed cycloisomerization of 1,8-diynyl vinyl acetates to bicycle[2.2.1]hept-2-en-7-ones. Catalyst used for the synthesis of spiro[piperidine-3,3'-oxindoles]. Catalyst used in the gold(I)-catalyzed Rautenstrauch rearrangement. Gold-catalyzed π-directed regioselective cyclization of bis(o-alkynyl benzyl alcohols): rapid excess to dihydroisobenzofuran derivatives. Gold compound used in acid-catalyzed cycloisomerization - synthesis of diverse nitrogen-containing spiro heterocycles. Gold catalyst used in the domino synthesis of functionalized benzofurans and tetracyclic isochromans via formal carboalkoxylation. Group: Gold series of catalysts. CAS No. 866395-16-6. Molecular formula: C20H15AuF6NO4PS2. Mole weight: 739.4. Appearance: white to off-white powder. Purity: 0.99. Catalog: ACM866395166.