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Merck
CN

M7379

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
PubChem Substance ID:
24897159
UNSPSC Code:
12161900
NACRES:
NA.25
EC Number:
246-675-7

Key Documents

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InChI key

HNXONNXIAJJXPE-UHFFFAOYSA-L

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

SMILES string

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

description

cationic

assay

≥98.0% (TLC)

mol wt

462.11 g/mol

technique(s)

electrophoresis: suitable

Quality Level

200

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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

signalword

Danger

hcodes

H302,H314

Hazard Classifications

Acute Tox. 4 Oral - Skin Corr. 1C

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCH9518
BCCH3520
BCCG4308
BCCB4923
BCBZ7019

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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)
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)
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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