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372099

Sigma-Aldrich

2,4-Di-tert-amylphenol

99%

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About This Item

Linear Formula:
[C2H5C(CH3)2]2C6H3OH
CAS Number:
120-95-6
Molecular Weight:
234.38
EC Number:
204-439-0
MDL number:
MFCD00041929
UNSPSC Code:
12352100
PubChem Substance ID:
24863017
NACRES:
NA.22

Assay

99%

bp

169-170 °C/22 mmHg (lit.)

mp

25 °C (lit.)

density

0.930 g/mL at 25 °C (lit.)

SMILES string

CCC(C)(C)c1ccc(O)c(c1)C(C)(C)CC

InChI

1S/C16H26O/c1-7-15(3,4)12-9-10-14(17)13(11-12)16(5,6)8-2/h9-11,17H,7-8H2,1-6H3

InChI key

WMVJWKURWRGJCI-UHFFFAOYSA-N

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General description

The standard molar enthalpies of sublimation (or vaporization) of 2,4-di-tert-amylphenol have been evaluated. Preparation of 2,4-di-tert-amylphenol, via catalytic alkylation of phenol with trimethylethylene, is reported.

Application

2,4-Di-tert-amylphenol is a phenolic compound, used for the laccase induced coupling reactions. It may be used in the synthesis of Cu-phthalocyanine-C60.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H319

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

372099-BULK:
372099-1L:
372099-VAR:

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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Molecular association and monolayer formation of soluble phthalocyanine compounds.
Viktorova EA, et al.
Russian Chemical Bulletin, 9(8), 1402-1402 (1960)
Enzymatic synthesis of Tinuvin.
Schroeder M, et al.
Enzyme and Microbial Technology, 40(7), 1748-1752 (2007)
Molecular association and monolayer formation of soluble phthalocyanine compounds.
Snow AW and Jarvis NL.
Journal of the Chemical Society, 106(17), 4706-4711 (1984)
Thermochemistry of phenols: quantification of the< i> ortho-,< i> para</i>-, and< i> meta</i>-interactions in tert-alkyl substituted phenols.
Verevkin SP.
The Journal of Chemical Thermodynamics, 31(5), 559-585 (1999)
Yan-Hua Liu et al.
Ecotoxicology and environmental safety, 135, 90-97 (2016-10-11)
The occurrence and distribution of eight selected endocrine-disrupting chemicals were investigated in samples of surface water and suspended particulate matter (SPM) in Nanjing section of Yangtze River over a year (the flow period, the wet period and the dry period).

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