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Merck

46405

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
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329757165
EC Number:
203-199-4
Beilstein/REAXYS Number:
2047450
MDL number:
MFCD00002396

Product Name

4-Nonylphenol, PESTANAL®, analytical standard

InChI key

IGFHQQFPSIBGKE-UHFFFAOYSA-N

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

SMILES string

CCCCCCCCCc1ccc(O)cc1

grade

analytical standard

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Quality Level

200

application(s)

agriculture
environmental

format

neat

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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.

General description

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

Legal Information

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

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

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB2704
STBL2684
STBK8893
STBK8892
STBK5758

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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
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
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
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