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45529

Supelco

2-Phenylphenol

PESTANAL®, analytical standard

Synonym(s):

2-Hydroxybiphenyl

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About This Item

Linear Formula:
C6H5C6H4OH
CAS Number:
Molecular Weight:
170.21
Beilstein:
606907
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
E Number:
E232
NACRES:
NA.24

grade

analytical standard

Quality Level

vapor pressure

7 mmHg ( 140 °C)

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

282 °C (lit.)

mp

57-59 °C (lit.)

application(s)

agriculture
cleaning products
cosmetics
environmental
flavors and fragrances
food and beverages
personal care

format

neat

SMILES string

Oc1ccccc1-c2ccccc2

InChI

1S/C12H10O/c13-12-9-5-4-8-11(12)10-6-2-1-3-7-10/h1-9,13H

InChI key

LLEMOWNGBBNAJR-UHFFFAOYSA-N

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General description

2-Phenylphenol is a bactericide, disinfectant and virucide with low levels of toxicity. It is commonly used in agriculture, for disinfecting fruits, eggs, and vegetables. 2-Phenylphenol also finds applications as a surface disinfectant in hospitals, veterinary centers, nursing homes, poultry farms, commercial laundries, food processing plants, dairy farms, etc.

Application

2-Phenylphenol may be used as an analytical reference standard for the quantification of the analyte in sewage, sludge, sediments and commercial formulations using chromatography techniques.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Other Notes

Ion Mobility: TWCCSN2 value of 133.9 Å2 [M-H]-

The collision cross section (CCS) measurement was provided by Waters Corporation, using the SYNAPT XS mass spectrometer.
For a description and overview of how ion mobility enables the measurement of the CCS of an ion visit ims.waters.com.
Further information on the SYNAPT XS mass spectrometer can be found on the IMS microsite and product webpage.

TWCCS measurements are expected to be within 2% of this reference value.

P/N 45529 is part of the Waters Extractables & Leachables UNIFI scientific library which can be downloaded from Waters Marketplace.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

The product is not intended for use as a biocide under global biocide regulations, including but not limited to US EPA′s Federal Insecticide Fungicide and Rodenticide Act, European Biocidal Products Regulation, Canada’s Pest Management Regulatory Agency, Turkey’s Biocidal Products Regulation, Korea’s Consumer Chemical Products and Biocide Safety Management Act (K-BPR) and others.

Signal Word

Danger

Hazard Statements

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

255.2 °F - closed cup

Flash Point(C)

124 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

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Determination of phenolic disinfectant agents in commercial formulations by liquid chromatography
Thompson RD
Journal of AOAC (Association of Official Analytical Chemists) International, 84(3), 815-822 (2001)
Determination of pharmaceuticals, steroid hormones, and endocrine-disrupting personal care products in sewage sludge by ultra-high-performance liquid chromatography--tandem mass spectrometry
Yu Y, et al.
Analytical and Bioanalytical Chemistry, 399(2), 891-902 (2011)
Guidelines for Drinking-water Quality, 1 (2004)
Determination of endocrine-disrupting phenols, acidic pharmaceuticals, and personal-care products in sewage by solid-phase extraction and gas chromatography--mass spectrometry
Lee BH, et al.
Journal of Chromatography A, 1094(1-2), 122-129 (2005)
Shusuke Tani et al.
Mutation research, 628(2), 123-128 (2007-01-26)
Oxidative mutation is mainly induced by reactive oxygen species (ROS), such as the superoxide anion radical (O(2)(-)) and hydrogen peroxide (H(2)O(2)). However, in Escherichia coli (E. coli), ROS are eliminated by enzymes such as superoxide dismutase and catalase, which are

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