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548618

Sigma-Aldrich

2-Benzyl-4-chlorophenol

95%

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Synonym(s):
Chlorophene
Linear Formula:
C6H5CH2C6H3(Cl)OH
CAS Number:
Molecular Weight:
218.68
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

95%

bp

160-162 °C (lit.)

mp

46-49 °C (lit.)

density

1.188 g/mL at 25 °C (lit.)

SMILES string

Oc1ccc(Cl)cc1Cc2ccccc2

InChI

1S/C13H11ClO/c14-12-6-7-13(15)11(9-12)8-10-4-2-1-3-5-10/h1-7,9,15H,8H2

InChI key

NCKMMSIFQUPKCK-UHFFFAOYSA-N

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Related Categories

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Eye Dam. 1 - Repr. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT RE 2 Oral

Target Organs

Kidney

WGK

WGK 2

Flash Point(F)

No data available

Flash Point(C)

No data available

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Gabriela Elizabeth Quintanilla-Villanueva et al.
Biosensors, 11(2) (2021-02-13)
Chlorophene is an important antimicrobial agent present in disinfectant products which has been related to health and environmental effects, and its detection has been limited to chromatographic techniques. Thus, there is a lack of research that attempts to develop new
L R Kao et al.
Biochemical pharmacology, 35(4), 613-620 (1986-02-15)
o-Benzyl-p-chlorophenol (BCP) is widely used as a broad spectrum disinfectant. Treatment of male Fischer 344 rats with BCP resulted in an increase in cytochrome P-450 content and an accompanying decrease in aryl hydrocarbon hydroxylase (AHH) activity in both liver and
W P Ridley et al.
Journal of toxicology and environmental health, 18(2), 267-283 (1986-01-01)
The metabolism and disposition of ortho-benzyl-para-chlorophenol (BCP) has been investigated in the male rat following an oral dose of 69 mg/kg or 206 mg/kg. BCP was rapidly eliminated at both dose levels with 45-49% of the dose appearing in the
Beatriz Merchel Piovesan Pereira et al.
Frontiers in microbiology, 12, 640923-640923 (2021-03-16)
Biocide use is essential and ubiquitous, exposing microbes to sub-inhibitory concentrations of antiseptics, disinfectants, and preservatives. This can lead to the emergence of biocide resistance, and more importantly, potential cross-resistance to antibiotics, although the degree, frequency, and mechanisms that give
L R Kao et al.
Journal of toxicology and environmental health, 18(3), 441-458 (1986-01-01)
The disposition and metabolism of o-benzyl-p-chlorophenol (BCP) were studied in male Fischer-344 rats. Three days after oral administration of [14C]BCP at 10, 100, or 1000 mg/kg, more than 90% of each dose was excreted in urine and feces. Comparison of

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