All Photos(1)
About This Item
Linear Formula:
H2NC6H3(C6H5)OH
CAS Number:
Molecular Weight:
185.22
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
grade
technical grade
Assay
90%
form
powder
mp
198-202 °C (lit.)
SMILES string
Nc1cc(ccc1O)-c2ccccc2
InChI
1S/C12H11NO/c13-11-8-10(6-7-12(11)14)9-4-2-1-3-5-9/h1-8,14H,13H2
InChI key
IGIDZGNPFWGICD-UHFFFAOYSA-N
General description
2-Amino-4-phenylphenol is an aminoalcohol derivative. It participates in the synthesis of bisbenzoxazoles.
Application
2-Amino-4-phenylphenol is suitable as an internal standard to investigate the enzymatic activity of N-hydroxy-N-2-fluorenylacetamide (N-OH-2-FAA), a mammary gland carcinogen in the female Sprague-Dawley rat, by HPLC.
It may be used as a chelating agent for metal ions.
It may be used as a chelating agent for metal ions.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Dermal - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
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’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Synthesis and properties of 4, 4'-bis [5-alkyl (aryl) benzoxazol-2-yl]-2-hydroxy (alkoxy) biphenyls.
Ol'khovik VK, et al.
Russ. J. Org. Chem., 42(8), 1164-1168 (2006)
Metal ion complexing properties of carcinogen metabolites.
J H WEISBURGER et al.
Biochemical pharmacology, 12, 179-191 (1963-02-01)
C L Ritter et al.
Carcinogenesis, 17(11), 2411-2418 (1996-11-01)
N-Hydroxy-N-2-fluorenylacetamide (N-OH-2-FAA) and its benzamide analogue N-OH-2-FBA are mammary gland carcinogens in the female Sprague-Dawley rat. Ovariectomy inhibits tumorigenicity of topically applied N-OH-2-FAA suggesting modulation of carcinogen-activating enzymes in the gland. This study concerned the activation of N-OH-2-FAA and N-OH-2-FBA
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service