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Merck
CN

442873

4-Nonylphenol

analytical standard

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About This Item

Empirical Formula (Hill Notation):
C15H24O
CAS Number:
Molecular Weight:
220.35
EC Number:
203-199-4
UNSPSC Code:
12181503
PubChem Substance ID:
Beilstein/REAXYS Number:
2047450
MDL number:
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InChI

1S/C15H24O/c1-2-3-4-5-6-7-8-9-14-10-12-15(16)13-11-14/h10-13,16H,2-9H2,1H3

InChI key

IGFHQQFPSIBGKE-UHFFFAOYSA-N

SMILES string

CCCCCCCCCc1ccc(O)cc1

grade

analytical standard

CofA

current certificate can be downloaded

packaging

ampule of 100 mg

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

application(s)

environmental

format

neat

storage temp.

2-30°C

Gene Information

mouse ... Esr1(13982)
rat ... Ar(24208)

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General description

This compound is listed in the SVHC (Substances of very high concern) candidate list of ECHA (European Chemicals Agency)

Analysis Note

Product 442873 is being discontinued. Product 46405 is available and may be an acceptable replacement.

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Repr. 2 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

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

Regulatory Information

危险化学品
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Urinary concentrations of bisphenol A and 4-nonylphenol in a human reference population.
Calafat MA, et al.
Environmental Health Perspectives, 113(4), 391-395 (2004)
Determination of the xenoestrogens 4-nonylphenol and bisphenol A by high-performance liquid chromatography and fluorescence detection after derivatisation with dansyl chloride.
Naassner, et al.
Journal of Chromatography A, 945(1-2), 133-138 (2002)
A H Shanthanagouda et al.
Comparative biochemistry and physiology. Toxicology & pharmacology : CBP, 157(2), 162-171 (2012-11-28)
This study investigated the influence of two endocrine disrupting chemicals (EDCs)-an exogenous oestrogen 17β-estradiol (E2) and the oestrogen mimic 4-n-nonylphenol (NP) on the expression of aromatase transcripts in both sexes of adult Murray river rainbowfish. Reproductively active mature fish were
Caixiang Zhang et al.
Journal of chromatography. A, 1230, 110-116 (2012-02-22)
4-Nonylphenols (4-NPs) are known endocrine disruptors and by-products of the microbial degradation of nonylphenol polyethoxylate surfactants. One of the challenges to understanding the toxic effects of nonylphenols is the large number of isomers that may exist in environmental samples. In
Fatemeh Navid et al.
The Journal of investigative dermatology, 133(12), 2763-2770 (2013-05-09)
UVR suppresses the immune system through the induction of regulatory T cells (Tregs). UVR-induced DNA damage has been recognized as the major molecular trigger involved, as reduction of DNA damage by enhanced repair prevents the compromise to the immune system

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