Search results
Results from the WOW.Com Content Network
Lauric acid, systematically dodecanoic acid, is a saturated fatty acid with a 12-carbon atom chain, thus having many properties of medium-chain fatty acids. [6] It is a bright white, powdery solid with a faint odor of bay oil or soap. The salts and esters of lauric acid are known as laurates.
It is the acid chloride of lauric acid. Lauroyl chloride is a standard reagent for installing the lauroyl group. [2] It is mainly produced as a precursor to dilauroyl peroxide, which is widely used in free-radical polymerizations. [3] Lauroyl chloride is a substrate for diverse reactions characteristic of acid chlorides.
Hazard statements form part of the Globally Harmonized System of Classification and Labelling of Chemicals (GHS). They are intended to form a set of standardized phrases about the hazards of chemical substances and mixtures that can be translated into different languages.
A colorless solid, it is often sold as a water-damped solid. It is the symmetrical peroxide of lauric acid. It is produced by treating lauroyl chloride with hydrogen peroxide in the presence of base: [2] 2 C 11 H 23 COCl + H 2 O 2 + 2 NaOH → (C 11 H 23 CO 2) 2 + 2 HCl
an identification of the product; one or more hazard pictograms (where necessary) a signal word – either Danger or Warning – where necessary; hazard statements, indicating the nature and degree of the risks posed by the product; the identity of the supplier (who might be a manufacturer or importer)
Hazard statements. H315, H318, H319, H335: ... As the sodium salt of a fatty acid (lauric acid), it is classified as a soap. It is a white solid. Use.
Chemical hazards are usually classified separately from biological hazards (biohazards). Chemical hazards are classified into groups that include asphyxiants, corrosives, irritants, sensitizers, carcinogens, mutagens, teratogens, reactants, and flammables. [1] In the workplace, exposure to chemical hazards is a type of occupational hazard.
Sodium lauroamphoacetate is produced in a 2 step process. Firstly lauric acid reacts with aminoethylethanolamine (AEEA); this initially produces the amide however heating causes this to cyclize to give the imidazoline group. This reacts with 1 equivalent of sodium chloroacetate to give the final product. A reaction with 2 equivalents gives the ...