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644-31-5

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644-31-5 Usage

Chemical Properties

Acetyl benzoyl peroxide is a white crystalline solid, forming needles.

Uses

Germicide; in bleaching of flour and food oils.

General Description

A solution containing less than 40% by mass of the white crystalline solid in a nonvolatile solvent. Dilution moderates reactivity of the pure solvent. Irritating to the skin, eyes and mucous membranes.

Air & Water Reactions

Decomposed by water [Hawley].

Reactivity Profile

Acetyl benzoyl peroxide SOLUTION [<= 40% PEROXIDE] is a powerful oxidizing agent. Reacts with reducing agents (including many common organic materials). These reactions may lead to ignition. Decomposes when heated.

Safety Profile

Poison by inhalation and ingestion. Severe irritant. A powerful oxidzing agent that is corrosive to the skin and mucous membranes. See also PEROXIDES, ORGANIC. Dangerous; shock or heat will cause detonation with evolution of toxic fumes; will react with water or steam to produce heat; can react vigorously with reducing materials. Flammable by spontaneous chemical reaction. To fight fire, use Con or dry chemical. When heated to decomposition it emits acrid smoke and fumes.

Potential Exposure

Used in disinfectants, to bleach flour; and in medications.

Shipping

UN3105 Organic peroxide type D, liquid, Hazard Class: 5.2; Labels: 5.2-Organic peroxide, Technical Name Required

Incompatibilities

Acetyl benzoyl peroxide is an organic peroxide which can detonate if shocked, heated, or on contact with contaminants. A powerful oxidizer. Violent reaction with many compounds, including reducing agents; chemically active metals; combustible materials, strong acids, alkaline earth sulfides, aluminum carbides, aluminum, amines, calcium sulfide, carbides, chlorine trifluoride, glycerin, hydrides, hydrochloric acid, hydrogen peroxide, hydrogen sulfide, hydroxylamine, magnesium, metal powders, metal sulfides, molybdenum, phenylhydrazine, phosphorous red/friction, phosphorous trichloride, silicon, sulfides, sulfur, sulfur dioxide, sulfur/friction, sulfuric acid, tungsten, hydrogen trisulfide. Avoid contact with moisture, water, steam, sources of ignition, combustible materials. Not compatible with strong bases; reducing materials; other oxidizers

Check Digit Verification of cas no

The CAS Registry Mumber 644-31-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,4 and 4 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 644-31:
(5*6)+(4*4)+(3*4)+(2*3)+(1*1)=65
65 % 10 = 5
So 644-31-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H8O4/c1-7(10)12-13-9(11)8-5-3-2-4-6-8/h2-6H,1H3

644-31-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name acetyl benzenecarboperoxoate

1.2 Other means of identification

Product number -
Other names Benzozone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:644-31-5 SDS

644-31-5Relevant articles and documents

Palladium-catalyzed ortho-functionalization of azoarenes with aryl acylperoxides

Qian, Cheng,Lin, Dongen,Deng, Yuanfu,Zhang, Xiao-Qi,Jiang, Huanfeng,Miao, Guang,Tang, Xihao,Zeng, Wei

, p. 5866 - 5875 (2014/08/05)

With the aid of an azo directing group, Pd-catalyzed ortho-sp2 C-H bond activation/functionalization of azoarenes with aryl acyl peroxides has been explored. This transformation provides easy access to regioselectively introducing acyloxyl and aryl groups into azoarenes by simply changing the reaction temperature and solvent. This journal is the Partner Organisations 2014.

Ozonolyses of acetylenes revisited

Griesbaum, Karl,Dong, Yuxiang

, p. 575 - 577 (2007/10/03)

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