
CAS 513-02-0: Triisopropyl phosphate
Formula:C9H21O4P
InChI:InChI=1S/C9H21O4P/c1-7(2)11-14(10,12-8(3)4)13-9(5)6/h7-9H,1-6H3
InChI key:InChIKey=OXFUXNFMHFCELM-UHFFFAOYSA-N
SMILES:P(OC(C)C)(OC(C)C)(OC(C)C)=O
Synonyms:- Isopropyl phosphate ((C<sub>3</sub>H<sub>7</sub>O)<sub>3</sub>PO)
- NSC 62275
- Nsc 46370
- Phosphoric acid, triisopropyl ester
- Phosphoric acid, tris(1-methylethyl) ester
- Phosphoric acid, tris(1-methylethyl) ester (9CI)
- Triisopropoxyphosphine oxide
- Tripropan-2-Yl Phosphate
- Isopropyl phosphate ((C3H7O)3PO)
- Triisopropyl phosphate
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Found 7 products.
Triisopropyl phosphate
CAS:Controlled ProductFormula:C9H21O4PColor and Shape:NeatMolecular weight:224.23Triisoproyl phosphate
CAS:Triisoproyl phosphate is a phosphatase inhibitor that is used in the preparation of polyvinylpolypyrrolidone (PVPP) or polyvinylpyrrolidone-coated nuclear magnetic resonance (NMR) sample tubes. Triisopropyl phosphate inhibits phosphatases, which are enzymes that catalyze the hydrolysis of ester bonds. This prevents the release of non-bound phosphate groups and results in a more stable polymer film. Triisopropyl phosphate has been shown to inhibit 5-HT2 receptors and trimethyl tryptamine in vitro, with an IC50 value of 3 μM. It also inhibits matrix metalloproteinases, which are enzymes that degrade the extracellular matrix and promote inflammation. The inhibition of these enzymes may be due to its ability to bind to and stabilize the active site by nucleophilic attack on the hydroxyl group. Triisopropyl phosphate has been shownPurity:Min. 95%Triisopropyl Phosphate
CAS:Controlled ProductApplications Triisopropyl Phosphate can be used as a flame retardant and catalyst. Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package References Zhang, Tie-jiang.: Meitan Jishu,29(2), 204-206 (2010);Chen, Yong-Fu, et al.: Jingxi Huagong, 17(9), 541-543 (2000)Formula:C9H21O4PColor and Shape:NeatMolecular weight:224.23