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153842

Sigma-Aldrich

4-tert-Amylphenol

99%

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About This Item

Formula condensata:
C2H5C(CH3)2C6H4OH
Numero CAS:
80-46-6
Peso molecolare:
164.24
Numero CE:
201-280-9
Numero MDL:
MFCD00002369
Codice UNSPSC:
12352100
ID PubChem:
24849381
NACRES:
NA.22

Saggio

99%

P. ebollizione

255 °C (lit.)

Punto di fusione

88-89 °C (lit.)

Solubilità

H2O: insoluble
alcohols: soluble
benzene: soluble
chloroform: soluble
diethyl ether: soluble

Stringa SMILE

CCC(C)(C)c1ccc(O)cc1

InChI

1S/C11H16O/c1-4-11(2,3)9-5-7-10(12)8-6-9/h5-8,12H,4H2,1-3H3
NRZWYNLTFLDQQX-UHFFFAOYSA-N

Informazioni sul gene

rat ... Ar(24208)

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Descrizione generale

A high performance liquid chromatography (HPLC) approach was studied for the determination of 4-tert-amylphenol.

Applicazioni

4-tert-Amylphenol was used as an esterogen receptor (ER) ligand.

Avvertenze

Danger

Indicazioni di pericolo

H302 + H312,H314,H317,H410

Classi di pericolo

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 1 - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1

Codice della classe di stoccaggio

8B - Non-combustible corrosive hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

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

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Certificati d'analisi (COA)

Lot/Batch Number
MKBX4272V
MKBS6872V
07912ED
11112PU
09020CQ

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José Zayas et al.
Journal of pharmaceutical and biomedical analysis, 41(2), 589-593 (2006-01-13)
A high performance liquid chromatography (HPLC) method for the detection of traces of LpHse (4-tert-amylphenol and 2-phenylphenol) has been developed and validated. The method was shown to be linear in the range from 0.5 to 10.00 ppm in solution. The
Hirofumi Yokota et al.
Aquatic toxicology (Amsterdam, Netherlands), 71(2), 121-132 (2005-01-12)
Alkylphenols including 4-tert-pentylphenol (4-PP) have been shown to alter sexual differentiation in fish due to their estrogenic properties. Medaka (Oryzias latipes) is so sensitive to these substances because morphological sex reversal and testis-ova induction are well developed in the exposed
Cédric Bovet et al.
Toxicology in vitro : an international journal published in association with BIBRA, 23(4), 704-709 (2009-02-24)
High-mass matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) combined with chemical cross-linking has the ability to monitor the ligand-dependent dimerization of the human estrogen receptor alpha ligand binding domain (hERalpha LBD) in solution. Because only ER ligands enhance the homodimer abundance
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Occupational vitiligo: clinical and epidemiological aspects.
C J Stevenson
The British journal of dermatology, 105 Suppl 21, 51-56 (1981-09-01)
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