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B97607

Sigma-Aldrich

2-tert-Butyl-6-methyl-phenol

99%

Synonym(s):

6-tert-Butyl-o-cresol

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About This Item

Linear Formula:
(CH3)3CC6H3(CH3)OH
CAS Number:
2219-82-1
Molecular Weight:
164.24
Beilstein/REAXYS Number:
1862362
EC Number:
218-734-7
MDL number:
MFCD00002239
UNSPSC Code:
12352100
PubChem Substance ID:
24892158
NACRES:
NA.22

assay

99%

form

crystals

refractive index

n20/D 1.519 (lit.)

bp

230 °C (lit.)

mp

24-27 °C (lit.)

density

0.967 g/mL at 25 °C (lit.)

SMILES string

Cc1cccc(c1O)C(C)(C)C

InChI

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

InChI key

BKZXZGWHTRCFPX-UHFFFAOYSA-N

Gene Information

human ... GABRA1(2554)

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pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

224.6 °F - closed cup

flash_point_c

107 °C - closed cup

ppe

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

Certificates of Analysis (COA)

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Jerry O Ebalunode et al.
Bioorganic & medicinal chemistry, 17(14), 5133-5138 (2009-06-13)
Current anesthetics, especially the inhaled ones, have troublesome side effects and may be associated with durable changes in cognition. It is therefore highly desirable to develop novel chemical entities that reduce these effects while preserving or enhancing anesthetic potency. In
Cynthia D Selassie et al.
Journal of medicinal chemistry, 48(23), 7234-7242 (2005-11-11)
In this comprehensive study on the caspase-mediated apoptosis-inducing effect of 51 substituted phenols in a murine leukemia cell line (L1210), we determined the concentrations needed to induce caspase activity by 50% (I50) and utilized these data to develop the following

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