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135321

Trimethylphenylammonium bromide

Name: Trimethylphenylammonium bromide
Brand: ALDRICH

98%, suitable for titration

Synonym(s):

Phenyltrimethylammonium bromide

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About This Item

Linear Formula:

(CH₃)₃N(Br)C₆H₅

CAS Number:

16056-11-4

Molecular Weight:

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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Properties

Product Name

Trimethylphenylammonium bromide, 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

Description

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

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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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

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

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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Global Trade Item Number

SKU	GTIN
135321-100G	04061838730626