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| Product | Description | |
|---|---|---|
| Triphenyl phosphate | quantitative NMR; Flame Retardants; Food Contact Materials. Uses: For analytical and research use. Group: Reagents. Alternative Names: Disflamoll TP, TP, Triphenyl phosphate, Wako TPP, DHPF 005, TTP, S 4 (phosphate), TPP, WSFR-TPP, Reofos TPP, TFF,Phosphoric acid, triphenyl ester, S 4, Celluflex TPP, NSC 57868, Phoscon FR 903N, TTP (triphenyl phosphate), Phenyl phosphate ((PhO)3PO), Phosflex TPP, Triphenoxyphosphine oxide, Triphenol phosphate, TPPA, Sumilizer TPP. CAS No. 115-86-6. Pack Sizes: 1G. IUPAC Name: triphenyl phosphate. |  |
| 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 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 (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 | 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 | 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-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. | Worldwide |
| Triphenyl phosphate-d15 | Triphenyl phosphate-d 15 is the deuterium labeled Triphenyl phosphate[1]. Uses: Scientific research. Group: Isotope-labeled compounds. Alternative Names: Celluflex TPP-d15; DHPF 005-d15; Disflamol TP-d15; Disflamoll TP-d15; NSC 57868-d15; Phenyl phosphate ((PhO)3PO)-d15; Phoscon FR 903N-d15. CAS No. 1173020-30-8. Pack Sizes: 2.5 mg. Product ID: HY-Y1322S. | |
| Triphenyl Phosphate-d15 | 2H Labeled Compounds. CAS No. 1173020-30-8. Molecular formula: C18D15O4P. Mole weight: 341.38. Catalog: ACM1173020308. |  |
| Triphenyl Phosphate-d15 | 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. | Worldwide |
| 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. | |
| Isopropylated Triphenyl Phosphate | Isopropylated Triphenyl Phosphate. CAS No: 26967-76-0 |  Sarchem Laboratories New Jersey NJ |
| Isopropylate Triphenyl Phosphate (IPPP 35 ) | Widely used for fabric coating, circuit boards, flooring, textiles, PVC, phenolic resin and other fields. Group: Phosphate ester flame retardant. Alternative Names: Isopropylate Triphenyl Phosphate ;Isopropyl Phenyl Diphenyl Phosphate;Tri(isopropylphenyl) Phosphate. CAS No. 68937-41-7. Molecular formula: C27H33O4P. Mole weight: 390. Appearance: Colorless or light yellow transparent liquid. Catalog: ACM68937417-4. | |
| (R)-(-)-3,3'-Bis(triphenylsilyl)-1,1'-binaphthyl-2,2'-diyl hydrogen phosphate, min. 98% [(R)-TiPSY] | A chiral phosphoric acid catalyst providing a convenient strategy for the enantioselective construction of protected primary amines and a highly stereoselective method for the reductive amination of heterocyclic amines. Chiral phosphoric acid used for the enantioselective Biginelli and Biginelli-like reactions. Chiral phosphoric acid organocatalyst used in the asymmetric, three-component Povarov reaction involving 2-hydroxystyrenes. An efficient method to access structurally diverse cis-disubstituted tetrahydroquinolines in high stereoselectivities of up to >99:1 dr and 97% ee. A gold/chiral phosphoric acid catalyst used for the highly stereoselective, three-component reaction of salicylaldehydes, anilines, and alkynols to give aromatic spiroacetals in high yields and stereoselectivities. The first highly enantioselective catalytic protocol for the reductive coupling of ketones and hydrozones. Reagent-controlled regioselectivity enabled by dual activation. Group: Organic phosphine compounds. Alternative Names: (S)-(+)-3,3'-Bis(triphenylsilyl)-1,1'-binaphthyl-2,2'-diyl hydrogen phosphate; RD-0080; (11bR)-4-Hydroxy-2,6-bis(triphenylsilyl)dinaphtho-[2,1-d:1 inverted exclamation marka,2 inverted exclamation markaf]-1,3,2-dioxaphosphepin 4-oxide; Carreira SALDIPAC Ligand; (R)-(-)-3,3'-Bis(triphenylsilyl)-1,1'-binaphthyl-2,2'-diyl hydrogen phosp | |
| (S)-(+)-3,3'-Bis(triphenylsilyl)-1,1'-binaphthyl-2,2'-diyl hydrogen phosphate, min. 98% [(S)-TiPSY] | Chiral phosphoric acid catalyst used for the highly enantioselective Friedel-Crafts reaction of indoles with imines. Chiral phosphoric acid catalyst used for the highly enantioselective Friedel-Crafts reaction of pyrrole derivatives with N-acyl imines. Chiral phosphoric acid catalyst used for the enantioselective transfer hydrogenation of hydroxylactams providing enantioenriched tetrahydro-β-carbolines (in dioxane) at room temperature (up to 94% yield, 90% ee). [Rh2(OAc)4]/chiral phosphoric acid catalyst used for the enantioselective symmetric, three-component reaction of diazo compounds with imines and water yielding β-amino-α-hydroxy acid derivatives. Enantioselective desymmetrization of prochiral allenic diols via cooperative catalysis of Pd(OAc)2 and a chiral phosphoric acid. Group: Phosphorus catalysts. Alternative Names: (11bS)-4-Hydroxy-2,6-bis(triphenylsilyl)dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepine4-oxide; Phosphoric acid (aR)-3,3'-bis(triphenylsilyl)-1,1'-binaphthalene-2,2'-diyl ester; (11bS)-4-Hydroxy-2,6-bis(triphenylsilyl)dinaphtho-[2,1-d1 inverted exclamation marka,2 inverted exclamation markaf]-[1,3,2]-dioxaphosphepin 4-oxide; (S)-3,3'-Bis(triphenylsilyl)-1,1'-binaphthyl-2,2'-diyl hydrogenphosphate. CAS No. 929097-92-7. Molecular formula: C56H41O4PSi2. Mole weight: 865.084g/mol. IUPACName: (13-hydroxy-1 | |
| 1-O-Trityl-sn-glycero-3-phosphocholine | Heterocyclic Organic Compound. Alternative Names: (4R)-4,7-Dihydroxy-N,N,N-trimethyl-1,1,1-triphenyl-2,6,8-trioxa-7-phosphadecan-10-aminium 7-Oxide Inner Salt; (7R)-4,7-Dihydroxy-N,N,N-trimethyl-10,10,10-triphenyl-3,5,9-trioxa-4-phosphadecan-1-aminium 4-Oxide Inner Salt. CAS No. 103675-56-5. Molecular formula: C27H35NO6P. Mole weight: 500.54. Appearance: White Solid. Purity: 0.96. IUPACName: [(2S)-2-hydroxy-3-trityloxypropyl] 2-(trimethylazaniumyl)ethyl phosphate. Catalog: ACM103675565. | |
| (3-Carboxypropyl)triphenylphosphonium Bromide | (3-Carboxypropyl)triphenylphosphonium Bromide is a reagent used for the preparation of sphingosine 1-phosphate-1 receptor antagonists, as well as for the synthesis of mitochondrial vitamin E metabolites and other mitochondrial targets in the study of mitochodrial functions. Synonyms: (4-Hydroxy-4-oxobutyl)triphenylphosphonium Bromide; Phosphonium, (3-carboxypropyl)triphenyl-, bromide (1:1). Grades: ≥95%. CAS No. 17857-14-6. Molecular formula: C22H22BrO2P. Mole weight: 429.29. |  |
| 5'-O-Tritylinosine | KIN59 is a purine riboside derivative that suppresses thymidine phosphorylase (TPase). TPase is an enzyme catalyzing the reversible phosphorolysis of pyrimidine deoxynucleosides to 2-deoxy-d-ribose-1-phosphate and their respective pyrimidine bases. KIN59 noncompetitively inhibits TPase-induced angiogenesis in the chorioallantoic membrane assay. Synonyms: 5'-Trt-rI; (2R,3R,4S,5R)-9-(3,4-Dihydroxy-5-trityloxymethyl-tetrahydrofuran-2-yl)-1,9-dihydropurin-6-one; KIN-59; Inosine, 5'-O-(triphenylmethyl)-; 5'-O-(triphenylmethyl)-inosine. Grades: ≥98% by HPLC. CAS No. 4152-77-6. Molecular formula: C29H26N4O5. Mole weight: 510.55. | |
| Malachite green hemioxalate | Malachite green hemioxalate (MCCK1) is a triphenylmethane dye which can be used to detect the release of phosphate in enzymatic reactions. Malachite green hemioxalate has antibacterial activity, which is attributed to inhibition of intracellular enzymes, insertion into DNA and/or interaction with cell membranes. Malachite green hemioxalate is also a potent and selective inhibitor of IKBKE , and inhibits its downstream targets such as IκBα , p65 and IRF3. Malachite green hemioxalate exhibits antitumor activity in vitro and in vivo [1] [2] [3]. Uses: Scientific research. Group: Fluorescent dye. Alternative Names: MCCK1. CAS No. 2437-29-8. Pack Sizes: 100 mg. Product ID: HY-D0162. | |
| [r-(Z)]-4-Hydroxy-N,N,N-trimethyl-9-oxo-7-[(triphenylmethoxy)methyl]-3,5,8-trioxa-4-phosphahexacos-17-en-1-aminium 4-oxide inner salt | Heterocyclic Organic Compound. Alternative Names: (7R,17Z)-4-Hydroxy-N,N,N-trimethyl-9-oxo-7-[(triphenylmethoxy)methyl]-3,5,8-trioxa-4-phosphahexacos-17-en-1-aminium 4-Oxide Inner Salt. CAS No. 103634-10-2. Molecular formula: C45H67NO7P. Mole weight: 764.99. Appearance: Pale Yellow Solid. Purity: 0.96. IUPACName: [(2R)-2-[(Z)-octadec-9-enoyl]oxy-3-trityloxypropyl] 2-(trimethylazaniumyl)ethyl phosphate. Canonical SMILES: CCCCCCCCC=CCCCCCCCC (=O)OC (COC (C1=CC=CC=C1) (C2=CC=CC=C2)C3=CC=CC=C3)COP (=O) ([O-])OCC[N+] (C) (C)C. Catalog: ACM103634102. | |
| 3-Carboxypropyl triphenylphosphonium bromide | (3-Carboxypropyl)triphenylphosphonium bromide is used as antimalarial agents, antimycobacterial agents,antifungal agents, inhibitors of protein tyrosine phosphatase. Group: Bromine series. Alternative Names: (4-Hydroxy-4-oxobutyl)triphenylphosphonium bromide. CAS No. 17857-14-6. Molecular formula: C22H22O2PBr. Mole weight: 429.29. Appearance: Solid. Purity: 0.98. IUPACName: 3-carboxypropyl(triphenyl)phosphanium; bromide. Canonical SMILES: C1=CC=C (C=C1)[P+] (CCCC (=O)O) (C2=CC=CC=C2)C3=CC=CC=C3. [Br-]. Catalog: ACM17857146-3. | |
| 5-Carboxypentyl triphenylphosphonium bromide | (5-Carboxypentyl)(triphenyl)phosphonium bromide is used in medicine and as pharmaceutical intermediate. It is also employed as catalyst. Reactant for: Preparation of inhibitor of protein tyrosine phosphatase 1B for treatment of diabetes and obesity. Synthesis of folate receptor-specific glycinamide ribonucleotide formyltransferase inhibitors with antitumor activity. Preparation of peptide nucleic acids (PNA) with high specific activity. Synthesis of roseophilin via Wittig/aldol methodology. Group: Organic phosphine compounds. Alternative Names: (5-Carboxypentyl)(Triphenyl)Phosphonium Bromide. CAS No. 50889-29-7. Molecular formula: C24H26BrO2P. Mole weight: 457.35. Appearance: Solid. Purity: 0.98. IUPACName: 5-carboxypentyl(triphenyl)phosphanium; bromide. Canonical SMILES: C1=CC=C (C=C1)[P+] (CCCCCC (=O)O) (C2=CC=CC=C2)C3=CC=CC=C3. [Br-]. Catalog: ACM50889297-3. | |
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