Cumyl Hydroperoxide CAS#80-15-9

Name: Cumyl Hydroperoxide CAS#80-15-9
SKU: 0

Classification：Catalysts And Auxiliaries

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product description

Cumyl Hydroperoxide CAS#80-15-9

Cumene hydroperoxide, an organic peroxide,is a colorless to pale yellow to green liquid. Mild odor.Molecular weight=152.21; Boiling point=153℃;Freezing/Melting point=2 10℃. It explodes on heating;Flash point=79℃. Its explosive limits are: LEL=0.9%;UEL=6.5%. Hazard Identification (based on NFPA-704 MRating System): Health 1, Flammability 2, Reactivity 4(Oxidizer). Slightly soluble in water.

Cumyl Hydroperoxide Chemical Properties

Melting point	-30 °C
Boiling point	100-101 °C/8 mmHg (lit.)
density	1.03 g/mL at 25 °C
vapor density	5.4 (vs air)
vapor pressure	<0.03 mm Hg ( 20 °C)
refractive index	n20/D1.5230
Fp	192 °C
storage temp.	2-8°C
solubility	Chloroform (Soluble), Ethyl Acetate (Slightly), Methanol (Soluble)
form	clear liquid
pka	pK1:12.60 (25°C)
color	Colorless to Almost colorless
PH	>5 (20°C, 13g/L in H2O)
Water Solubility	Slightly soluble
BRN	1908117
Exposure limits	No exposure limit is set. On the basis of its irritant properties, a ceiling limit of 2 mg/m3 (0.3 ppm) is recommended.
Stability:	Stable. combustible. Strong oxidizer. Incompatible with a variety of organic materials, reacting vigorously or violently with acids, reducing agents, many metals, strong alkalies. Heat sensitive, decomposing explosively.
LogP	1.6 at 25℃
CAS DataBase Reference	80-15-9(CAS DataBase Reference)
NIST Chemistry Reference	Hydroperoxide, 1-methyl-1-phenylethyl(80-15-9)
EPA Substance Registry System	Cumene hydroperoxide (80-15-9)

Safety Information

Hazard Codes	O,T,N
Risk Statements	7-21/22-23-34-48/20/22-51/53-66-65-10-37
Safety Statements	14-3/7-36/37/39-45-50-61-14A-26-62-47-7
RIDADR	UN 3109 5.2
WGK Germany	3
RTECS	MX2450000
TSCA	Yes
HazardClass	5.2
PackingGroup	II
HS Code	29096000
Hazardous Substances Data	80-15-9(Hazardous Substances Data)

Product Usage

Cumene Hydroperoxide is used in the preparation of polystyrene nanocapsules. It acts as a curing agent for polyester resins and as an oxidizer in organic chemical reactions. It serves as an initiator for radical polymerization especially for acrylate and methacrylate monomers. It also employed as an intermediate in the cumene process for developing phenol and acetone from benzene and propene. Further, it is used as an epoxidation reagent for allylic alcohols and fatty acid esters. In addition to this, it is also used to prepare methylstyrene, acetophenone and cumyl alcohol

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