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53751

Benzethonium chloride

BioUltra, ≥99.0% (AT)

Synonyme(s) :

(Diisobutylphenoxyethoxyethyl)dimethylbenzylammonium chloride, Phemerol chloride

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A propos de cet article

Formule empirique (notation de Hill) :
C27H42ClNO2
Numéro CAS:
Poids moléculaire :
448.08
UNSPSC Code:
12161900
NACRES:
NA.25
PubChem Substance ID:
EC Number:
204-479-9
Beilstein/REAXYS Number:
3898548
MDL number:
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description

cationic

Quality Level

product line

BioUltra

assay

≥99.0% (AT)

form

(Powder, Colorless or White)

mol wt

448.08 g/mol

impurities

insoluble matter, passes filter test, ≤5% water

pH

5.5-7.5 (25 °C, 0.1 M in H2O)

mp

162-164 °C (lit.)

solubility

H2O: 0.1 M at 20 °C, clear, colorless

anion traces

sulfate (SO42-): ≤50 mg/kg

cation traces

Al: ≤5 mg/kg, Ba: ≤5 mg/kg, Bi: ≤5 mg/kg, Ca: ≤10 mg/kg, Cd: ≤5 mg/kg, Co: ≤5 mg/kg, Cr: ≤5 mg/kg, Cu: ≤5 mg/kg, Fe: ≤5 mg/kg, K: ≤50 mg/kg, Li: ≤5 mg/kg, Mg: ≤5 mg/kg, Mn: ≤5 mg/kg, Mo: ≤5 mg/kg, Na: ≤50 mg/kg, Ni: ≤5 mg/kg, Pb: ≤5 mg/kg, Sr: ≤5 mg/kg, Zn: ≤5 mg/kg

absorption

cut-off at 300 nm in H2O at 0.1 M

application(s)

(Pharmaceuticals/personal care)
(Pharmaceuticals/personal care)

SMILES string

[Cl-].CC(C)(C)CC(C)(C)c1ccc(OCCOCC[N+](C)(C)Cc2ccccc2)cc1

InChI

1S/C27H42NO2.ClH/c1-26(2,3)22-27(4,5)24-13-15-25(16-14-24)30-20-19-29-18-17-28(6,7)21-23-11-9-8-10-12-23;/h8-16H,17-22H2,1-7H3;1H/q+1;/p-1

InChI key

UREZNYTWGJKWBI-UHFFFAOYSA-M

General description

The benzethonium chloride is a well characterized skin irritant and rare sensitizer.

Application

Benzethonium chloride has been used in a study to assess the minimum inhibitory concentrations of meticillin-resistant Staphylococcus aureus (MRSA) isolates from Malaysia. It has also been used in a study to prepare biocomposite films from sodium alginate and modified clay.

Disclaimer

The product is not intended foruse as a biocide under global biocide regulations, including but not limited toUS EPA′s Federal Insecticide Fungicide and Rodenticide Act, European BiocidalProducts Regulation, Canada’s Pest Management Regulatory Agency, Turkey’sBiocidal Products Regulation, Korea’s Consumer Chemical Products and BiocideSafety Management Act (K-BPR) and others.

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Cet article
B8879PHR14251051500
form

(Powder, Colorless or White)

form

powder

form

-

form

powder

assay

≥99.0% (AT)

assay

≥97% (titration), ≥98% (HPLC)

assay

-

assay

-

application(s)

(Pharmaceuticals/personal care)
(Pharmaceuticals/personal care)

application(s)

microbiology (topical antiseptic)

application(s)

pharmaceutical (small molecule)

application(s)

USP Biologics
pharmaceutical (small molecule)

cation traces

Al: ≤5 mg/kg, Bi: ≤5 mg/kg, Cd: ≤5 mg/kg, Cr: ≤5 mg/kg, Fe: ≤5 mg/kg, Li: ≤5 mg/kg, Mn: ≤5 mg/kg, Na: ≤50 mg/kg, Pb: ≤5 mg/kg, Zn: ≤5 mg/kg, Ba: ≤5 mg/kg, Co: ≤5 mg/kg, K: ≤50 mg/kg, Mo: ≤5 mg/kg, Sr: ≤5 mg/kg, Ca: ≤10 mg/kg, Mg: ≤5 mg/kg, Cu: ≤5 mg/kg, Ni: ≤5 mg/kg

cation traces

-

cation traces

-

cation traces

-

mol wt

448.08 g/mol

mol wt

448.08 g/mol

mol wt

-

mol wt

-

impurities

insoluble matter, passes filter test, ≤5% water

impurities

-

impurities

-

impurities

-


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Danger

Hazard Classifications

Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Corr. 1B

Classe de stockage

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 2

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges



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T Ichikawa et al.
Journal of dentistry, 36(11), 965-968 (2008-09-10)
The purpose of this study was to evaluate if the sugar alcohols erythritol, xylitol and sorbitol enhance the fungicidal effect of benzethonium chloride (BTC) toward in vitro candidal biofilms. An in vitroCandida albicans biofilm was formed on a plastic coverslip
Elisabeth Lang et al.
Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology, 28(2), 347-354 (2011-08-26)
Benzethonium, an antimicrobial surfactant widely used as preservative of pharmaceuticals, topical wound care product and oral disinfectant, triggers apoptosis of several cell types. The apoptosis is preceded and possibly triggered by mitochondrial depolarization. Even though lacking mitochondria, erythrocytes may similarly
Brandon Findlay et al.
Bioorganic & medicinal chemistry letters, 22(4), 1499-1503 (2012-01-31)
Here we present a proof-of-concept study, combining two known antimicrobial agents into a hybrid structure in order to develop an emergent cationic detergent-like interaction with the bacterial membrane. Six amphiphilic conjugates were prepared by copper (I)-catalyzed 1,3-dipolar cycloaddition between a



Numéro d'article de commerce international

RéférenceGTIN
15200-50ML04061838740083
53751-50G04061835541508
53751-250G04061835541492

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