Skip to Content
MilliporeSigma
All Photos(1)

Documents

74202

Supelco

Tetramethylammonium chloride

suitable for ion pair chromatography, LiChropur™, ≥99.0% (AT)

Synonym(s):

TMA

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
(CH3)4N(Cl)
CAS Number:
75-57-0
Molecular Weight:
109.60
Beilstein/REAXYS Number:
3911201
EC Number:
200-880-8
MDL number:
MFCD00011628
UNSPSC Code:
12000000
PubChem Substance ID:
329765550
NACRES:
NB.21

description

cationic

Quality Level

100

assay

≥99.0% (AT)

form

crystals

quality

LiChropur™

technique(s)

ion pair chromatography: suitable

mp

>300 °C (lit.)

λ

10 % in H2O

UV absorption

λ: 220 nm Amax: 0.05
λ: 230 nm Amax: 0.04
λ: 250 nm Amax: 0.03
λ: 260 nm Amax: 0.02
λ: 500 nm Amax: 0.02

suitability

corresponds to standard for RP gradient test
corresponds to standard for filter test

SMILES string

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

InChI

1S/C4H12N.ClH/c1-5(2,3)4;/h1-4H3;1H/q+1;/p-1

InChI key

OKIZCWYLBDKLSU-UHFFFAOYSA-M

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

Tetramethylammonium chloride (TMAC) is structurally similar to alkyltrimethylammonium salts. Oxidation of TMAC yields formaldehyde and trimethlamine. It is considered as poor phase-transfer catalyst for most reactions as it is insoluble in organic media. However, it is highly suitable as phase-transfer catalyst for fluorination of chlorobenzaldehydes along with alkali metal fluorides which yield 1,2,2,2-tetrafluoroethyldifluoromethyl ether.

Application

TMAC may be used in ion-exchange procedures to show the increase of pH in understanding the chemical behaviour of catalyst [CTA]Si-MCM-41 using Knoevenagel condensation model.

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

signalword

Danger

Hazard Classifications

Acute Tox. 2 Oral - Acute Tox. 3 Dermal - Aquatic Chronic 2 - Skin Irrit. 2 - STOT SE 1 Oral

target_organs

Central nervous system

Storage Class

6.1A - Combustible, acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 1

ppe

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCBV0084
BCBR8642V
BCBR8643V
BCBR8640V
BCBR8636V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 6

1 of 6

BIS-TRIS propane ≥99.0% (titration)

Sigma-Aldrich

B6755

BIS-TRIS propane

Tetramethylammonium bromide ACS reagent, ≥98.0%

Sigma-Aldrich

426296

Tetramethylammonium bromide

Sodium chloride for HPLC LiChropur™

Supelco

5.43832

Sodium chloride

Tetraethylammonium chloride ≥98% (titration)

Sigma-Aldrich

T2265

Tetraethylammonium chloride

Tetramethylammonium bromide 98%

Sigma-Aldrich

195758

Tetramethylammonium bromide

Tetramethylammonium hydroxide pentahydrate ≥97%

Sigma-Aldrich

T7505

Tetramethylammonium hydroxide pentahydrate

Fundamentals, Applications, and Industrial Perspectives
C.M. Starks, M. Halper
Phase Transfer Catalysis (Academic Press), 182-182 (2012)
Surfactant containing Si-MCM-41: An efficient basic catalyst for the Knoevenagel condensation.
Martins, Leandro, et al.
Applied Catalysis A: General, 312, 77-85 (2006)
Markus Welcker et al.
Genes & development, 27(23), 2531-2536 (2013-12-04)
The Fbw7 tumor suppressor targets a broad network of proteins for ubiquitylation. Here we show critical functions for Fbw7 dimerization in regulating the specificity and robustness of degradation. Dimerization enables Fbw7 to target substrates through concerted binding to two suboptimal
Wei Shen et al.
Chemical communications (Cambridge, England), 49(73), 8114-8116 (2013-08-08)
A simple and low-cost colorimetric assay utilizing ferrofluidic nanoparticulate probes (FNPs) and a ligase for single-nucleotide polymorphism genotyping is described. Excellent sensitivity and selectivity were accomplished through the engagement of the FNPs and a ligase chain reaction.
Marco I Ries et al.
The Journal of biological chemistry, 288(52), 37289-37295 (2013-11-15)
Metabolic profiling and structural elucidation of novel secondary metabolites obtained from derived deletion strains of the filamentous fungus Penicillium chrysogenum were used to reassign various previously ascribed synthetase genes of the roquefortine/meleagrin pathway to their corresponding products. Next to the
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service