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Merck
모든 사진(2)

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

분석

95%

refractive index

n20/D 1.4070 (lit.)

bp

224 °C (lit.)

density

0.970 g/mL at 25 °C (lit.)

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

유사한 제품을 찾으십니까? 방문 제품 비교 안내

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

FlameSkull and crossbonesEnvironment

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

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

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point (°F)

73.4 °F - closed cup

Flash Point (°C)

23 °C - closed cup

개인 보호 장비

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


시험 성적서(COA)

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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

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)
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)
The effect of triisopropyl phosphate on the mobility of surface concanavalin A receptors and on the locomotion of polymorphonuclear leucocytes.
A M Woodin et al.
Experimental cell research, 94(2), 292-298 (1975-09-01)
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)

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