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Merck
CN

247049

Sigma-Aldrich

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:
分子量:
202.32
Beilstein:
1738261
EC 号:
MDL编号:
UNSPSC代码:
12352128
PubChem化学物质编号:
NACRES:
NA.22
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产品名称

三丁基膦, mixture of isomers, 97%

蒸汽密度

9 (vs air)

方案

97%

表单

liquid

自燃温度

392 °F

反应适用性

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

杂质

<1% TBP oxide
5% TBP isomers

折射率

n20/D 1.462 (lit.)

沸点

150 °C/50 mmHg (lit.)

密度

0.81 g/mL at 25 °C (lit.)

官能团

phosphine

SMILES字符串

CCCCP(CCCC)CCCC

InChI

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

InChI key

TUQOTMZNTHZOKS-UHFFFAOYSA-N

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应用

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。

警示用语:

Danger

危险分类

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

储存分类代码

4.2 - Pyrophoric and self-heating hazardous materials

WGK

WGK 2

闪点(°F)

242.6 °F - closed cup

闪点(°C)

117 °C - closed cup

个人防护装备

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

法规信息

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分析证书(COA)

Lot/Batch Number

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J. Mol. Catal. A: Chem., 271, 145-145 (2007)
Yin-Wei Sun et al.
Organic letters, 12(24), 5664-5667 (2010-11-13)
P(n)Bu(3)-catalyzed cyclization reactions of salicylaldimines and salicylaldehydes with ethyl 2,3-butadienoate gave the corresponding functionalized chromans in moderate to good yields in THF under mild conditions. The new reaction provides a new method for the synthesis of biologically active chroman products.
E Kaniowska et al.
Journal of chromatography. A, 798(1-2), 27-35 (1998-05-02)
Several human diseases, in particular metabolic disorders, often lead to the accumulation of characteristic metabolites in plasma, urine and cells. The selected diseases of this type include cystinuria and homocystinuria. In the typical laboratory diagnosis of these two diseases, a
Tien Q Pham et al.
The Journal of organic chemistry, 70(16), 6369-6377 (2005-07-30)
The phosphine-catalyzed [3 + 2]-cycloaddition of 5-methylenehydantoins 4 with the ylides 5, derived from addition of tributylphosphine to the 2-butynoic acid derivatives, 6a-d, gives spiro-heterocyclic products. The camphor sultam derivative 6b gives optically active products. Noteable was that the ylides
Cristina-Maria Vâlcu et al.
Proteomics, 6(5), 1599-1605 (2006-02-04)
Protein extraction procedure and the reducing agent content (DTT, dithioerythritol, tributyl phosphine and tris (2-carboxyethyl) phosphine (TCEP)) of the sample and rehydration buffers were optimised for European beech leaves and roots and Norway spruce needles. Optimal extraction was achieved with

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