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28250

Cumene hydroperoxide

technical, ~80% in cumene

Synonym(s):

α,α-Dimethylbenzyl hydroperoxide

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About This Item

Linear Formula:
C6H5C(CH3)2OOH
CAS Number:
80-15-9
Molecular Weight:
152.19
PubChem Substance ID:
329753108
UNSPSC Code:
12352000
Beilstein/REAXYS Number:
1908117
MDL number:
MFCD00002129
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vapor density

5.4 (vs air)

vapor pressure

<0.03 mmHg ( 20 °C)

grade

technical

reaction suitability

reagent type: oxidant

concentration

~80% in cumene

refractive index

n20/D 1.519

bp

100-101 °C/8 mmHg (lit.)

density

1.028 g/mL at 20 °C

storage temp.

2-8°C

SMILES string

CC(C)(OO)c1ccccc1

InChI

1S/C9H12O2/c1-9(2,11-10)8-6-4-3-5-7-8/h3-7,10H,1-2H3

InChI key

YQHLDYVWEZKEOX-UHFFFAOYSA-N

Other Notes

Sales restrictions may apply

signalword

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 2 - Asp. Tox. 1 - Carc. 1B - Eye Dam. 1 - Flam. Liq. 3 - Org. Perox. F - Skin Corr. 1B - STOT RE 2 Inhalation - STOT SE 3

target_organs

Lungs, Respiratory system

Storage Class

5.2 - Organic peroxides and self-reacting hazardous materials

wgk

WGK 2

flash_point_f

127.4 °F

flash_point_c

53 °C

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Regulatory Information

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Wei Zhang et al.
Biochimica et biophysica acta, 1850(4), 742-749 (2014-12-30)
Organic isothiocyanates (ITCs) are produced by plants, in which they are released from glucosinolates by myrosinase. ITCs are generally toxic and serve as a chemical defense against herbivorous insects and against infections by microorganisms. In mammalian tissues subtoxic concentrations of
John P Hale et al.
Biophysical journal, 101(8), 1921-1929 (2011-10-19)
We investigate the effect of oxidative stress on red blood cell membrane mechanical properties in vitro using detailed analysis of the membrane thermal fluctuation spectrum. Two different oxidants, the cytosol-soluble hydrogen peroxide and the membrane-soluble cumene hydroperoxide, are used, and
Yu Jin Choi et al.
Dalton transactions (Cambridge, England : 2003), 40(10), 2234-2241 (2011-01-25)
A copper(II)-hydroperoxo complex, [Cu(Me(6)-tren)(OOH)](+) (2), and a copper(ii)-cumylperoxo complex, [Cu(Me(6)-tren)(OOC(CH(3))(2)Ph)](+) (3), were synthesized by reacting [Cu(Me(6)-tren)(CH(3)CN)](2+) (1) with H(2)O(2) and cumyl-OOH, respectively, in the presence of triethylamine. These intermediates, 2 and 3, were successfully characterized by various physicochemical methods such
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