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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

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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

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

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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

Signal Word

Danger

Hazard Statements

H302,H314

Hazard Classifications

Acute Tox. 4 Oral - Skin Corr. 1C

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

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’.

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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

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