Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

M7379

Sigma-Aldrich

Methylbenzethonium chloride

Synonym(s):

N,N-Dimethyl-N-(2-[2-(methyl-4-[1,1,3,3-tetramethylbutyl]phenoxy)ethoxy]ethyl)benzylammonium chloride

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

About This Item

Linear Formula:
C28H44NO2Cl
CAS Number:
25155-18-4
Molecular Weight:
462.11
EC Number:
246-675-7
UNSPSC Code:
12161900
PubChem Substance ID:
24897159
NACRES:
NA.25

description

cationic

Quality Level

200

assay

≥98.0% (TLC)

mol wt

462.11 g/mol

technique(s)

electrophoresis: suitable

SMILES string

[Cl-].Cc1cc(ccc1OCCOCC[N+](C)(C)Cc2ccccc2)C(C)(C)CC(C)(C)C

InChI

1S/2C28H44NO2.2ClH/c1-23-20-25(14-15-26(23)28(5,6)22-27(2,3)4)31-19-18-30-17-16-29(7,8)21-24-12-10-9-11-13-24;1-23-20-25(28(5,6)22-27(2,3)4)14-15-26(23)31-19-18-30-17-16-29(7,8)21-24-12-10-9-11-13-24;;/h2*9-15,20H,16-19,21-22H2,1-8H3;2*1H/q2*+1;;/p-2

InChI key

HNXONNXIAJJXPE-UHFFFAOYSA-L

Looking for similar products? Visit Product Comparison Guide

Application

Methylbenzethonium chloride has been used in a study to assess stem cell death-inducing small molecules. It has also been used in a study to investigate the anti-leishmanial activity of paromomycin ointment (Leshcutan) combined with the immunomodulator Imiquimod.

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

hcodes

H302,H314

Hazard Classifications

Acute Tox. 4 Oral - Skin Corr. 1C

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

Leishmania major: in vitro and in vivo anti-leishmanial activity of paromomycin ointment (Leshcutan) combined with the immunomodulator Imiquimod
El-On, J., et al.
Experimental Parasitology, 116, 7-7 (2007)
Successful topical treatment of murine cutaneous leishmaniasis with a combination of paromomycin (Aminosidine) and gentamicin
Grogl, M., et al.
Parasitology Research, 85, 254-259 (1999)
De-Hao Tsai et al.
Analytical and bioanalytical chemistry, 404(10), 3015-3023 (2012-10-30)
Dithiothreitol (DTT)-based displacement is widely utilized for separating ligands from their gold nanoparticle (AuNP) conjugates, a critical step for differentiating and quantifying surface-bound functional ligands and therefore the effective surface density of these species on nanoparticle-based therapeutics and other functional

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