Inhalation may cause lung oedema. May react explosively upon contact with reducing reagents. vapor density 5.4 (vs air) vapor pressure <0.03 mmHg ( 20 °C) assay ~80% bp 100-101 °C/8 mmHg (lit.) The technical product can contain a certain amount of cumene (10-20%) which changes physical properties. Burning sensation. A peroxol that is cumene in which the alpha-hydrogen is replaced by a hydroperoxy group. CopyCopied, Validated by Experts, Validated by Users, Non-Validated, Removed by Users, Predicted data is generated using the ACD/Labs Percepta Platform - PhysChem Module, Predicted data is generated using the US Environmental Protection Agency’s EPISuite™, Click to predict properties on the Chemicalize site, For medical information relating to Covid-19, please consult the, https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:78673, ACD/Labs Percepta Platform - PhysChem Module, US Environmental Protection Agency’s EPISuite™, Compounds with the same molecular formula, Search Google for structures with same skeleton, 100-102 deg C / 8 mm (259.1367-261.9117 °C / 760 mmHg), 100-102 °C / 8 mm (259.1367-261.9117 °C / 760 mmHg), 100-101 °C / 8 mmHg (259.1367-260.5243 °C / 760 mmHg), DANGER: OXIDIZER, CORROSIVE, burns skin and eyes, OXIDISER / HARMFUL TO THE ENVIRONMENT / TOXIC. Chemical dangers Transportation

[2] Products of decomposition of cumene hydroperoxide are methylstyrene, acetophenone, and cumyl alcohol. A peroxol that is cumene in which the alpha-hydrogen is replaced by a hydroperoxy group.

Burning sensation. Refer for medical attention . Heat of decomposition and initial exothermic temperature of cumene hydroperoxide. Abdominal pain. May decompose violently on contact with cobalt, copper or lead alloys and mineral acids. Can be exploded by shock or heat [Sax, 2 ed., 1965, p. 643]. EYES: First check the victim for contact lenses and remove if present. [3] Its formula is C6H5C(CH3)2OOH. Do not transport with food and feedstuffs. (USCG, 1999). Separated from combustible substances, reducing agents, mineral acids and food and feedstuffs. May also indicate that the same chemical with the same CAS number appears on another list with a different chemical name. Readily capable of detonation or explosive decomposition or explosive reaction at normal temperatures and pressures. The cumene process (cumene–phenol process, Hock process) is an industrial process for synthesizing phenol and acetone from benzene and propylene.The term stems from cumene (isopropyl benzene), the intermediate material during the process. This generates fire and explosion hazard. Decomposes explosively with sodium iodide [Chem.

Personal protection: chemical protection suit including self-contained breathing apparatus.

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,1-2 H3 InChI key YQHLDYVWEZKEOX-UHFFFAOYSA-N First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention. Above 79°C use a closed system and ventilation. Above 79°C explosive vapour/air mixtures may be formed. Symptoms may be delayed. Inhalation of vapor causes headache and burning throat.

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