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199168

Trimethylphenylammonium chloride

Name: Trimethylphenylammonium chloride
Brand: ALDRICH

≥98%, solid

Synonym(s):

Phenyltrimethylammonium chloride

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About This Item

Linear Formula:

(CH₃)₃N(Cl)C₆H₅

CAS Number:

138-24-9

Molecular Weight:

171.67

NACRES:

NA.22

PubChem Substance ID:

24851895

UNSPSC Code:

12352107

EC Number:

205-319-0

MDL number:

MFCD00011790

Beilstein/REAXYS Number:

3572527

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Properties

Product Name

Trimethylphenylammonium chloride, ≥98%

Quality Level

100

assay

≥98%

form

solid

reaction suitability

core: ammonium

mp

246-248 °C (dec.) (lit.)

SMILES string

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

InChI

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

InChI key

MQAYPFVXSPHGJM-UHFFFAOYSA-M

Description

pictograms

GHS06

signalword

Danger

hcodes

H301 + H311,H412

pcodes

P264 - P273 - P280 - P301 + P310 - P302 + P352 + P312 - P361 + P364

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Aquatic Chronic 3

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 2

flash_point_f

327.2 °F - closed cup

flash_point_c

164 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

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Synthesis and Characterization of Clay Polymer Nanocomposites of P(4VP-co-AAm) and Their Application for the Removal of Atrazine.

Jorge A Ramírez-Gómez et al.

Polymers, 11(4) (2019-04-24)

Atrazine (ATZ) is an herbicide which is applied to the soil, and its mechanism of action involves the inhibition of photosynthesis. One of its main functions is to control the appearance of weeds in crops, primarily in corn, sorghum, sugar

Headspace gas chromatography based methodology for the analysis of aromatic substituted quaternary ammonium salts.

Niels van Boxtel et al.

Journal of chromatography. A, 1476, 105-113 (2016-11-26)

The analysis of quaternary ammonium salts (QAS) using GC is often performed by "in injector" pyrolysis to create volatile degradation products for quantification purposes. Besides the risk of severe system contamination, the application of this approach on aqueous samples is

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

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Global Trade Item Number

SKU	GTIN
199168-100G	04061838763020