2,4-Bis(α,α-diMethylbenzyl)phenol

Names

[ Name ]:
2,4-Bis(α,α-diMethylbenzyl)phenol

[Synonym ]:
2,4 DI-CUMYLPHENOL
Phenol, 2,4-bis(1-methyl-1-phenylethyl)-
2,4-Di-α-cumylphenol
2,4-Bis(α,α-dimethylbenzyl)phenol
2,4-Bis(2-phenylpropan-2-yl)phenol
2,4-BIS(ALPHA,ALPHA-DIMETHYLBENZYL)PHENOL
EINECS 220-466-0
MFCD00191242
2,4-Bis(2-phenyl-2-propanyl)phenol
2,4-Bis(1-methyl-1-phenylethyl)phenol

Chemical & Physical Properties

[ Density]:
1.063

[ Boiling Point ]:
441.1±14.0 °C at 760 mmHg

[ Melting Point ]:
63-65 °C(lit.)

[ Molecular Formula ]:
C₂₄H₂₆O

[ Molecular Weight ]:
330.463

[ Flash Point ]:
204.9±12.0 °C

[ Exact Mass ]:
330.198364

[ PSA ]:
20.23000

[ LogP ]:
6.85

[ Vapour Pressure ]:
0.0±1.1 mmHg at 25°C

[ Index of Refraction ]:
1.579

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H319-H413

[ Precautionary Statements ]:
P305 + P351 + P338

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
26-27-28.1-36/39

[ Safety Phrases ]:
S26-S27-S28-S36/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2907199090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2907199090

[ Summary ]:
2907199090 other monophenols VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%

Articles

2,4-Bis(alpha,alpha-dimethylbenzyl)phenol

Acta Crystallogr. C 56 (Pt 8) , 1046-7, (2000)

The structure of the title compound, 2, 4-bis(1-methyl-1-phenylethyl)phenol, C(24)H(26)O, was found to have a torsion angle of 129.95 (13) degrees for the C-C bond that connects the benzyl carbon to t...

Application of a mathematical topological pattern of antihistaminic activity for the selection of new drug candidates and pharmacology assays.

J. Med. Chem. 49(12) , 3667-73, (2006)

Molecular topology was used to achieve a mathematical model capable of classifying compounds according to their antihistaminic activity and low sedative effects. By application of this model of activi...

A highly efficient catalyst for the “living” and “immortal” polymerization of e-caprolactone and L-lactide. Liu Y-C, et al.

Macromolecules 34(18) , 6196-6201, (2001)