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Merck
CN

199168

Trimethylphenylammonium chloride

≥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

Key Documents

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Product Name

Trimethylphenylammonium chloride, ≥98%

InChI key

MQAYPFVXSPHGJM-UHFFFAOYSA-M

InChI

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

SMILES string

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

assay

≥98%

form

solid

mp

246-248 °C (dec.) (lit.)

Quality Level

100

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Related Categories

pictograms

Skull and crossbones
GHS06

signalword

Danger

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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Certificates of Analysis (COA)

Lot/Batch Number
SDBB2423
STBK5080
STBK4752
STBK4416
STBK1365

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Jorge A Ramírez-Gómez et al.
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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
R W Gullick et al.
Environmental science & technology, 35(7), 1523-1530 (2001-05-12)
A natural shale and four synthetic organoclays were compared as potential sorbent additives to containment barriers at hazardous waste sites. Trimethylphenyl ammonium bentonite (TMPA-bent) was shown in batch experiments to have the greatest sorption capacities for 1,2,4-trichlorobenzene, trichloroethylene, and methyl
Alec N Salt et al.
Hearing research, 182(1-2), 24-33 (2003-09-02)
Our understanding of the perilymph kinetics of drugs depends largely on data obtained by the analysis of perilymph samples. Although a number of studies have demonstrated qualitatively that perilymph samples may be contaminated by cerebrospinal fluid (CSF), and some investigations
Jie Zhang et al.
Journal of chromatography. A, 1216(44), 7527-7532 (2009-04-07)
A method has been established for the determination of four pharmaceutically active compounds (ibuprofen, ketoprofen, naproxen and clofibric acid) in water samples using dynamic hollow fiber liquid-phase microextraction (HF/LPME) followed by gas chromatography (GC) injection port derivatization and GC-mass spectrometric
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