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C87800

Sigma-Aldrich

4-Cumylphenol

99%

Synonym(s):

4-(2-Phenylisopropyl)phenol

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About This Item

Linear Formula:
C6H5C(CH3)2C6H4OH
CAS Number:
599-64-4
Molecular Weight:
212.29
EC Number:
209-968-0
MDL number:
MFCD00002365
UNSPSC Code:
12352100
PubChem Substance ID:
24893104
NACRES:
NA.22

Assay

99%

form

crystals

bp

335 °C (lit.)

mp

74-76 °C (lit.)

SMILES string

CC(C)(c1ccccc1)c2ccc(O)cc2

InChI

1S/C15H16O/c1-15(2,12-6-4-3-5-7-12)13-8-10-14(16)11-9-13/h3-11,16H,1-2H3

InChI key

QBDSZLJBMIMQRS-UHFFFAOYSA-N

Gene Information

rat ... Ar(24208)

Related Categories

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Yichang Chen et al.
PLoS genetics, 12(7), e1006223-e1006223 (2016-07-30)
Concerns about the safety of Bisphenol A, a chemical found in plastics, receipts, food packaging and more, have led to its replacement with substitutes now found in a multitude of consumer products. However, several popular BPA-free alternatives, such as Bisphenol
Jaeseong Jeong et al.
International journal of molecular sciences, 20(5) (2019-03-13)
Molecular docking is used to analyze structural complexes of a target with its ligand for understanding the chemical and structural basis of target specificity. This method has the potential to be applied for discovering molecular initiating events (MIEs) in the
Zong-Da Du et al.
Talanta, 206, 120179-120179 (2019-09-14)
In this work, the magnetic amino-functionalized microporous organic network composites (Fe3O4@MON-NH2) were rational designed and facile synthesized for magnetic solid phase extraction (MSPE) of endocrine disrupting chemicals (EDCs), followed by their analysis with high-performance liquid chromatography. The incorporation of amino
Xiaoxia Wang et al.
Environmental toxicology, 35(5), 628-638 (2020-01-10)
Bisphenol A (BPA) and 4-cumylphenol (4-CP), as estrogen-like chemicals, are ubiquitous in the environment media and associated with the occurrence and development of hormone-dependent tumors. However, the combinatorial effects of these two structurally similar alkylphenols are not well informed. In
Cecilie N Ramskov Tetzlaff et al.
Environmental toxicology, 35(5), 543-552 (2019-12-11)
Bisphenol A (BPA) has been widely reported to exert endocrine disrupting effects, including the induction of adipogenesis in cultured preadipocytes and intact animals. Because of the potential harm to human health, BPA is being substituted by structurally related bisphenols. Whether
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