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Diethylene glycol monoethyl ether (2-(2-ethoxyethoxy)ethanol, carbitol cellosolve, CH 3 CH 2 OCH 2 CH 2 OCH 2 CH 2 OH) Diethylene glycol mono-n-butyl ether (2-(2-butoxyethoxy)ethanol, butyl carbitol, CH 3 CH 2 CH 2 CH 2 OCH 2 CH 2 OCH 2 CH 2 OH) Dipropyleneglycol methyl ether; C12-15 pareth-12 a polyethylene glycol ether used as an emulsifier ...
Dipropylene glycol finds many uses as a plasticizer, an intermediate in industrial chemical reactions, as a polymerization initiator or monomer, and as a solvent.Its low toxicity and solvent properties make it an ideal additive for perfumes and skin and hair care products.
Estimates on the prevalence of propylene glycol allergy range from 0.8% (10% propylene glycol in aqueous solution) to 3.5% (30% propylene glycol in aqueous solution). [ 70 ] [ 71 ] [ 72 ] The North American Contact Dermatitis Group (NACDG) data from 1996 to 2006 showed that the most common site for propylene glycol contact dermatitis was the ...
Diethylene glycol butyl ether (2-(2-butoxyethoxy)ethanol) is the organic compound with the formula C 4 H 9 OC 2 H 4 OC 2 H 4 OH. A colorless liquid, it is common industrial solvent. It is one of several glycol ether solvents. It has low odour and high boiling point.
Di(propylene glycol) methyl ether is an organic solvent with a variety of industrial and commercial uses. [2] [3] It finds use as a less volatile alternative to propylene glycol methyl ether and other glycol ethers. The commercial product is typically a mixture of four isomers. [4]
n-Butyl glycidyl ether is an industrial chemical used in adhesives, sealants, and as a paint or coating additive. It is principally used to reduce the viscosity of epoxy resin systems. [ 4 ]
This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.
As is typical of ethers, dipropyl ether may slowly form explosive organic peroxides over long periods in storage. [2] Antioxidants such as butylated hydroxytoluene are often added to ethers to prevent this process. [4] Due to the shock and light sensitive nature of organic peroxides, dipropyl ether should never be boiled or evaporated to dryness.