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Merck
모든 사진(2)

주요 문서

554669

Sigma-Aldrich

Triisopropyl phosphate

95%

동의어(들):

NSC 46370, NSC 62275, Phosphoric acid triisopropyl ester

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About This Item

Linear Formula:
PO(OCH(CH3)2)3
CAS Number:
Molecular Weight:
224.23
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

분석

95%

refractive index

n20/D 1.4070 (lit.)

bp

224 °C (lit.)

density

0.970 g/mL at 25 °C (lit.)

작용기

phosphate

SMILES string

CC(C)OP(=O)(OC(C)C)OC(C)C

InChI

1S/C9H21O4P/c1-7(2)11-14(10,12-8(3)4)13-9(5)6/h7-9H,1-6H3

InChI key

OXFUXNFMHFCELM-UHFFFAOYSA-N

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일반 설명

Triisopropyl phosphate, an ester of secondary alcohol, is a non-phosphorylating organophosphorus compound. It is formed as a by-product during the synthesis of haloalkylphosphonates. Triisopropyl phosphate can be prepared from isopropyl alcohol by reacting with phosphorus oxychloride. It can also be obtained from triisopropyl phosphite.

픽토그램

Skull and crossbonesEnvironment

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 3 Oral - Aquatic Acute 1 - Eye Irrit. 2

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point (°F)

141.8 °F - closed cup - (own results)

Flash Point (°C)

61 °C - closed cup - (own results)

개인 보호 장비

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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문서 라이브러리 방문

Physicochemical characteristics and sorption capacities of heavy metal ions of activated carbons derived by activation with different alkyl phosphate triesters
Wang J, et al.
Applied Surface Science, 316, 443-450 (2014)
Efficient and `green?microwave-assisted synthesis of haloalkylphosphonates via the Michaelis?Arbuzov reaction.
Jansa P, et al.
Green Chemistry, 13(4), 882-888 (2011)
Reactions of Trialkyl Phosphates, Alkyl Acetates, and Tertiary Butyl Hypochlorite in the Friedel-Crafts Syntheses1.
Berman N and Lowy A.
Journal of the American Chemical Society, 60(11), 2596-2597 (1938)
Dealkylation and debenzylation of triesters of phosphoric acid. Phosphorylation of hydroxy and amino compounds.
Zervas L and Dilaris I.
Journal of the American Chemical Society, 77(20), 5354-5357 (1955)
Carbonium ion formation in solvolysis of phosphate triesters.
Cox Jr JR and Newton MG.
The Journal of Organic Chemistry, 34(9), 2600-2605 (1969)

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