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46405

Supelco

4-Nonylphenol

PESTANAL®, analytical standard

Synonym(s):

4-n-Nonylphenol

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About This Item

Empirical Formula (Hill Notation):
C15H24O
CAS Number:
104-40-5
Molecular Weight:
220.35
Beilstein:
2047450
EC Number:
203-199-4
MDL number:
MFCD00002396
UNSPSC Code:
41116107
PubChem Substance ID:
329757165
NACRES:
NA.24

grade

analytical standard

Quality Level

200

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

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

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

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

Signal Word

Danger

Hazard Statements

H302,H314,H361,H410

Hazard Classifications

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

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
STBL2684
STBK8892
STBK8893
STBK5758
STBK0306

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4-Hexylphenol ≥98.0% (HPLC)

Sigma-Aldrich

778508

4-Hexylphenol

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
Mohammad Naderi et al.
Environmental toxicology, 29(4), 459-465 (2012-03-22)
Nonylphenol (NP) is an endocrine disrupting chemical which has been shown to be able to modulate the endocrine system of various organisms by different mechanisms. The objective of this study was to investigate the potential effects of 4-NP on steroid
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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