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135321

苯基三甲基溴化铵

Name: 苯基三甲基溴化铵
Brand: ALDRICH

98%, suitable for titration

别名:

三甲基苯基溴化铵

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关于此项目

线性分子式:

(CH₃)₃N(Br)C₆H₅

化学文摘社编号:

16056-11-4

分子量:

216.12

NACRES:

NA.22

PubChem Substance ID:

24848077

UNSPSC Code:

12352116

EC Number:

240-202-8

MDL number:

MFCD00011788

Beilstein/REAXYS Number:

3917006

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属性

产品名称

苯基三甲基溴化铵, 98%

assay

98%

form

powder

reaction suitability

core: ammonium

technique(s)

titration: suitable

mp

215 °C (dec.) (lit.)

SMILES string

[Br-].C[N+](C)(C)c1ccccc1

InChI

1S/C9H14N.BrH/c1-10(2,3)9-7-5-4-6-8-9;/h4-8H,1-3H3;1H/q+1;/p-1

InChI key

GNMJFQWRASXXMS-UHFFFAOYSA-M

说明

pictograms

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

历史批次信息供参考:

分析证书(COA)

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Effect of overall charge and charge distribution on cellular uptake, distribution and phototoxicity of cationic porphyrins in HEp2 cells.

Timothy J Jensen et al.

Journal of photochemistry and photobiology. B, Biology, 100(2), 100-111 (2010-06-19)

Five cationic porphyrins bearing one to four -N(CH(3))(3)(+) groups linked to the p-phenyl positions of 5,10,15,20-tetraphenylporphyrin (TPP) were synthesized in order to study the effect of overall charge and its distribution on the cellular uptake, phototoxicity and intracellular localization using

Screening and optimization of the derivatization of polar herbicides with trimethylanilinium hydroxide for GC-MS analysis.

A Ranz et al.

Journal of biochemical and biophysical methods, 69(1-2), 3-14 (2006-03-28)

In the present study, a derivatization method for the determination of acidic herbicides has been investigated. This procedure involves the methylation with the quaternary ammonium salt trimethylanilinium hydroxide (TMAH) directly in the gas chromatographic auto-sampler vial for analysis by gas

Cobalamin-dependent methionine synthase: probing the role of the axial base in catalysis of methyl transfer between methyltetrahydrofolate and exogenous cob(I)alamin or cob(I)inamide.

Jeanne Sirovatka Dorweiler et al.

Biochemistry, 42(49), 14653-14662 (2003-12-10)

Cobalamin-dependent methionine synthase (MetH) catalyzes the transfer of methyl groups between methyltetrahydrofolate (CH(3)-H(4)folate) and homocysteine, with the enzyme-bound cobalamin serving as an intermediary in the methyl transfers. An MetH fragment comprising residues 2-649 contains modules that bind and activate CH(3)-H(4)folate

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全球贸易项目编号

货号	GTIN
135321-100G	04061838730626