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384445

Sigma-Aldrich

4-Octylphenol

99%

Sinonimo/i:

4-Octylphenol, 4-n-Octylphenol, p-(n-Octyl)phenol, p-Octylphenol

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About This Item

Formula condensata:
CH3(CH2)7C6H4OH
Numero CAS:
1806-26-4
Peso molecolare:
206.32
Numero CE:
217-302-5
Numero MDL:
MFCD00036134
Codice UNSPSC:
12352100
ID PubChem:
24863997
NACRES:
NA.22

Saggio

99%

Forma fisica

solid

P. eboll.

150 °C/4 mmHg (lit.)

Punto di fusione

44-45 °C (lit.)

Densità

0.961 g/mL at 25 °C (lit.)

Stringa SMILE

CCCCCCCCc1ccc(O)cc1

InChI

1S/C14H22O/c1-2-3-4-5-6-7-8-13-9-11-14(15)12-10-13/h9-12,15H,2-8H2,1H3
NTDQQZYCCIDJRK-UHFFFAOYSA-N

Informazioni sul gene

rat ... Ar(24208)

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Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H315,H319

Classi di pericolo

Eye Irrit. 2 - Skin Irrit. 2

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

235.4 °F - closed cup

Punto d’infiammabilità (°C)

113 °C - closed cup

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
MKCP9386
MKCC6434
MKBW6803V
MKBR5305V
MKBL2960V

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Yu-Hai Liu et al.
Huan jing ke xue= Huanjing kexue, 35(6), 2209-2215 (2014-08-28)
The 206 nm irradiation from excilamp was able to directly photo-degrade 4-nonylphenol (4-NP) and 4-octylphenol (4-OP), but it could not oxidize them completely into CO2. Under the same irradiation condition, the removal efficiency of 4-OP was higher than that of
G G Kuiper et al.
Endocrinology, 139(10), 4252-4263 (1998-09-29)
The rat, mouse and human estrogen receptor (ER) exists as two subtypes, ER alpha and ER beta, which differ in the C-terminal ligand-binding domain and in the N-terminal transactivation domain. In this study, we investigated the estrogenic activity of environmental
Tao Lv et al.
Journal of separation science, 37(19), 2757-2763 (2014-07-22)
A novel hyphenated method based on ultrasound-assisted dispersive liquid-liquid microextraction coupled to precolumn derivatization has been established for the simultaneous determination of bisphenol A, 4-octylphenol, and 4-nonylphenol by high-performance liquid chromatography with fluorescence detection. Different parameters that influence microextraction and
R White et al.
Endocrinology, 135(1), 175-182 (1994-07-01)
We show that a number of alkylphenolic compounds, used in a variety of commercial products and found in river water, are estrogenic in fish, birds, and mammals. 4-Octylphenol (OP), 4-nonylphenol, 4-nonylphenoxycarboxylic acid, and 4-nonylphenoldiethoxylate were each capable of stimulating vitellogenin
Carme Valls-Cantenys et al.
Journal of separation science, 37(24), 3706-3713 (2014-10-10)
Simple, precise, and low-cost methods for the simultaneous determination of phenolic endocrine disrupting compounds such as bisphenol A, trichlorophenol, pentachlorophenol, 4-nonylphenol, and 4-octylphenol in water samples were developed. The Direct, in situ derivatization methods are based on polydimethylsiloxane rod extraction
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