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442873

Supelco

4-Nonylphenol

analytical standard

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About This Item

Empirical Formula (Hill Notation):
C15H24O
CAS Number:
104-40-5
Molecular Weight:
220.35
Beilstein/REAXYS Number:
2047450
EC Number:
203-199-4
MDL number:
MFCD00002396
UNSPSC Code:
12181503
PubChem Substance ID:
24868032

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

SMILES string

CCCCCCCCCc1ccc(O)cc1

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

Gene Information

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

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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_germany

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

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Certificates of Analysis (COA)

Lot/Batch Number
LC26769V
LC24619V
LC18178V
LC13683V
LC10337V

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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)
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
Irina Gyllenhammar et al.
Environment international, 43, 21-28 (2012-04-03)
4-Nonylphenol (NP) and bisphenol A (BPA) are phenolic substances used in high volumes by the industry. Studies on cells and in experimental animals have shown that both these compounds can be classified as estrogenic hormone disrupters. Information about the exposure
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
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
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