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Merck
CN

247049

三丁基膦

97%, liquid, mixture of isomers

别名:

P(n-Bu)3, TBP

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关于此项目

线性分子式:
[CH3(CH2)3]3P
化学文摘社编号:
998-40-3
分子量:
202.32
NACRES:
NA.22
PubChem Substance ID:
329752742
UNSPSC Code:
12352128
EC Number:
213-651-2
MDL number:
MFCD00009462
Beilstein/REAXYS Number:
1738261

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产品名称

三丁基膦, mixture of isomers, 97%

InChI key

TUQOTMZNTHZOKS-UHFFFAOYSA-N

InChI

1S/C12H27P/c1-4-7-10-13(11-8-5-2)12-9-6-3/h4-12H2,1-3H3

SMILES string

CCCCP(CCCC)CCCC

vapor density

9 (vs air)

assay

97%

form

liquid

autoignition temp.

392 °F

reaction suitability

reaction type: Buchwald-Hartwig Cross Coupling Reaction, reaction type: Heck Reaction, reaction type: Hiyama Coupling, reaction type: Negishi Coupling, reaction type: Sonogashira Coupling, reaction type: Stille Coupling, reaction type: Suzuki-Miyaura Coupling, reagent type: ligand
reaction type: Acetylations, reagent type: ligand
reaction type: Addition Reactions, reagent type: ligand
reaction type: Stille Coupling

impurities

<1% TBP oxide, 5% TBP isomers

refractive index

n20/D 1.462 (lit.)

bp

150 °C/50 mmHg (lit.)

density

0.81 g/mL at 25 °C (lit.)

functional group

phosphine

Quality Level

200

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相关类别

Application

1,4-加成催化剂；与二硫化物配合用于醇的硫醚化；酰化催化剂；用于制备活性酯。
与铂(II) 或铂(IV) 一起用于未活化的烯烃的分子间氢胺化反应。

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Pyr. Liq. 1 - Skin Corr. 1A

存储类别

4.2 - Pyrophoric and self-heating hazardous materials

wgk

WGK 2

flash_point_f

242.6 °F - closed cup

flash_point_c

117 °C - closed cup

ppe

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

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
SHBT3647
SDBB4930
SDBB3685
SDBB3131
SHBR5334

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J. Mol. Catal. A: Chem., 271, 145-145 (2007)
J Krijt et al.
Clinical chemistry, 47(10), 1821-1828 (2001-09-25)
Aminothiols have been implicated in the pathogenesis of arteriosclerosis, and reliable methods are needed to determine their concentrations in body fluids. We present a comparison of two analytical methods and focus on the reduction of low-molecular weight and protein-mixed disulfides
Jing-Yu Wu et al.
The Journal of organic chemistry, 73(22), 9137-9139 (2008-10-24)
Aziridines underwent cyclization reaction with carbon disulfide and isothiocyanate in the presence of organophosphine to afford thiazolidinone derivatives in good to high yields. The mechanistic study revealed that organophosphine serves as a catalyst in the reaction.
J X Yan et al.
Journal of chromatography. A, 813(1), 187-200 (1998-08-11)
A simple technique is introduced to identify and quantitate cysteine (Cys) after acid hydrolysis of protein. The technique involves using 9-fluorenylmethyl chloroformate (Fmoc)-based amino acid analysis that recovers all of the amino acids (asparagine and glutamine are recovered in their
Bradley G Jellerichs et al.
Journal of the American Chemical Society, 125(26), 7758-7759 (2003-06-26)
Upon exposure of mono-enone mono-allylic carbonates to tributylphosphine and 1 mol % Pd(Ph3P)4, efficient conversion to the corresponding cycloallylated products is achieved. This transformation combines the nucleophilic features of the Morita-Baylis-Hillman reaction with the electrophilic features of the Trost-Tsuji reaction.
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