Used in production of acetone and phenol, as a polymerization catalyst, in redox systems. Controlled incineration with flue gas scrubbing is possible for combustible packaging materials. Cumene hydroperoxide is an organic hydroperoxide intermediate in the cumene process for synthesizing phenol and acetone from benzene and propene. It has one double bond, and is the second simplest member of the alkene class of hydrocarbons. ALPHA,ALPHA-DIMETHYLBENZENE HYDROPEROXIDE, HYDROPEROXIDE, ALPHA,ALPHA-DIMETHYLBENZYL. Inhalation of vapor causes headache and burning throat. Hence sinks in water. Z Avoid dust formation. Continue rinsing. Do not let product enter drains. [4] Oxidation of cumene affords cumene hydroperoxide. Substance Name: Cumene hydroperoxideRN: 80-15-9UNII: PG7JD54X4IInChIKey: YQHLDYVWEZKEOX-UHFFFAOYSA-N. 8(8), Pg. Nearly all the cumene that is produced as a pure compound on an industrial scale is converted to cumene hydroperoxide, which is an intermediate in the synthesis of other industrially important chemicals, primarily phenol and acetone. This compound exists as a deliquescent colorless solid with a camphor-like odor, which, when very pure, melts near room temperature. Phenolic compounds are classified as simple phenols or polyphenols based on the number of phenol units in the molecule. P301+P312 IF SWALLOWED: Call a POISON CENTER/doctor/…if you feel unwell. W Use proper glove removal technique(without touching glove's outer surface) to avoid skin contact with this product. U It is classified as a weak acid since it only partially dissociates in solution, but concentrated acetic acid is corrosive and can attack the skin. combustible. Can be exploded by shock or heat [Sax, 2 ed., 1965, p. 643]. Sweep up and shovel. This technology was commercialized by Sumitomo Chemical. Pick up and arrange disposal. It is typically used as an oxidizing agent. An epoxide is a cyclic ether with a three-atom ring. Belongs to the Following Reactive Group(s). 7 For precautions see section 2.2. This section provides a listing of alternate names for this chemical, P270 Do not eat, drink or smoke when using this product. CopyCopied, InChI=1S/C9H12O2/c1-9(2,11-10)8-6-4-3-5-7-8/h3-7,10H,1-2H3 P210 Keep away from heat, hot surfaces, sparks, open flames and other ignition sources. [4] Oxidation of cumene affords cumene hydroperoxide. 205, 1958. Incompatible with a variety of organic materials, reacting vigorously or violently with acids, reducing agents, many metals, strong alkalies. Acetophenone is the organic compound with the formula C6H5C(O)CH3 (also represented by the pseudoelement symbols PhAc or BzMe). Cumene hydroperoxide; (Isopropylbenzene hydroperoxide) (80-15-9) 0.15 ppm : 1.6 ppm : 9.7 ppm : LEL = 9000 ppm Toxic by inhalation and skin absorption. Allyl alcohol is used as a raw material for the production of glycerol, but is also used as a precursor to many specialized compounds such as flame-resistant materials, drying oils, and plasticizers. Allyl alcohol (IUPAC name: prop-2-en-1-ol) is an organic compound with the structural formula CH2=CHCH2OH. 22, 1961. L (USCG, 1999). Avoid exposure - obtain special instructions before use.Provide appropriate exhaust ventilation at places where dust is formed. Avoid breathing vapours, mist or gas. It is typically used as an oxidizing agent. Violent reaction occurs upon contact with copper, copper alloys, lead alloys, and mineral acids. Chemical Encyclopedia It is more toxic than typical small alcohols. Consult a physician. P302+P352 IF ON SKIN: Wash with plenty of water/... P312 Call a POISON CENTER/doctor/…if you feel unwell. This ring approximates an equilateral triangle, which makes it strained, and hence highly reactive, more so than other ethers. Hydroperoxides or peroxols are compounds containing the hydroperoxide functional group (ROOH). 5 Avoid formation of dust and aerosols.