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13954

苄基三丁基溴化铵

Name: 苄基三丁基溴化铵
Brand: ALDRICH

≥99.0%, solid

别名:

Benzyltri-n-butylammonium bromide, Tributylbenzylammonium bromide

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关于此项目

线性分子式:

C₆H₅CH₂N(Br)(CH₂CH₂CH₂CH₃)₃

化学文摘社编号:

25316-59-0

分子量:

356.38

NACRES:

NA.22

PubChem Substance ID:

57647124

UNSPSC Code:

12352116

EC Number:

246-819-9

MDL number:

MFCD00011848

Beilstein/REAXYS Number:

3776294

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属性

产品名称

苄基三丁基溴化铵, ≥99.0%

Quality Level

200

assay

≥99.0%

form

solid

reaction suitability

core: ammonium

mp

169-175 °C

SMILES string

[Br-].CCCC[N+](CCCC)(CCCC)Cc1ccccc1

InChI

1S/C19H34N.BrH/c1-4-7-15-20(16-8-5-2,17-9-6-3)18-19-13-11-10-12-14-19;/h10-14H,4-9,15-18H2,1-3H3;1H/q+1;/p-1

InChI key

UDYGXWPMSJPFDG-UHFFFAOYSA-M

说明

Application

Benzyltributylammonium bromide can be used:

As a phase transfer catalyst in the isomerization reactions of cis-4-formyl-2-azetidinones.
As a hydrogen-bond acceptor in the preparation of deep eutectic solvents, which are used in the isolation of lysozyme from the chicken egg white.
In the phase transfer glycosylation of novobiocin to yield glucosyl-novobiocin.

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

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分析证书(COA)

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Regioselective glycosylation of novobiocin alters activity

Sun G, et al.

Carbohydrate Research, 452(11), 116-121 (2017)

Base-Promoted Isomerization of cis-4-Formyl-2-azetidinones: Chemoselective C 4-Epimerization vs Rearrangement to Cyclic Enaminones

Alcaide B, et al.

The Journal of Organic Chemistry, 65(11), 3453-3459 (2000)

Development of deep eutectic solvent-based aqueous biphasic system for the extraction of lysozyme

Xu P, et al.

Talanta, 202(11), 1-10 (2019)

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全球贸易项目编号

货号	GTIN
13954-50G	04061833013885