Adjective:

অম্ল পদার্থ-সংক্রান্ত,

tartaric's Usage Examples:

Three primary acids are found in wine grapes: tartaric, malic, and citric acids.

Louis Pasteur found to be a mixture of the two enantiomeric isomers of tartaric acid.

It is an ester formed from coumaric acid and tartaric acid.

composed of caffeic acid, a hydroxycinnamate produced by plants, and tartaric acid, the principal organic acid found in grape berries.

example shown below, the meso form of tartaric acid forms a diastereomeric pair with both levo and dextro tartaric acids, which form an enantiomeric pair.

active pair of levotartaric acid (L-(R,R)-(+)-tartaric acid) and dextrotartaric acid (D-(S,S)-(-)-tartaric acid).

A tartrate is a salt or ester of the organic compound tartaric acid, a dicarboxylic acid.

Inactive ingredients include menthol, tartaric acid, and propylene glycol.

, the enantiomers of tartaric acid, whose crystallized enantiomers were separated with tweezers by Pasteur).

acid acetic acid formic acid citric acid oxalic acid uric acid malic acid tartaric acid In general, organic acids are weak acids and do not dissociate completely.

This material is the source for most commercial tartaric acid, which is used in cooking and in organic chemistry.

DATEM (diacetyl tartaric acid ester of mono- and diglycerides, also E472e) is an emulsifier primarily used in baking to strengthen the gluten network in.

tartaric acid, this results in a glass-ionomer in liquid form.

An aqueous solution of maleic acid polymer or maleic/acrylic copolymer with tartaric acid.

food ingredient that is used to impart a sour flavor, made from citric or tartaric acid and sugar.

Racemic acid is an old name for an optically inactive or racemic form of tartaric acid.

coating of invert sugar and sour sugar (a combination of citric acid, tartaric acid, and sugar).

It is the aluminium salt of acetic acid and tartaric acid.

acid during ripening makes tartaric acid the predominant acid; grape berries also possess a small amount of citric acid.

glaucum was found by Pasteur to feed on only one enantiomer of tartaric acid, L-(+)-tartaric acid, which makes its use the earliest example of kinetic resolution.