DL-Mandelic acid

Research use only, not for human use.

It is an isomer of cresotinic acid (2-hydroxy-3-methylbenzoic acid) and oxymethylbenzoic acid (2-methoxybenzoic acid). Derivatives of mandelic acid are formed as a result of metabolism of adrenaline and noradrenaline by monoamine oxidase and catechol-o-methyl transferase.

It is an isomer of cresotinic acid (2-hydroxy-3-methylbenzoic acid) and oxymethylbenzoic acid (2-methoxybenzoic acid). Derivatives of mandelic acid are formed as a result of metabolism of adrenaline and noradrenaline by monoamine oxidase and catechol-o-methyl transferase. It is also present in certain skin care products is an intermediate molecule in the production of other biochemicals may be used as an analytical reagent and is a precursor in the manufacture of dyes. Mandelic acid is found to be associated with phenylketonuria which is an inborn error of metabolism.

Mandelic acid ((±)-Mandelic acid) exhibits significant sperm-immobilizing effects and caused mild plasma membrane injury, suggesting that it has potential for development as a future non-surfactant spermicide.Mandelic acid, an alpha-hydroxyacid derived from the hydrolysis of an extract of bitter almonds, has been studied extensively for its possible uses in health care products, such as photoaging, irregular pigmentation, and antimicrobial.

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acidomandelico

Proteasome/Ubiquitin

Endogenous Metabolite

others

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90-64-2

152.15

C8H8O3

>98% (HPLC)

DMSO:10 mM

OC(C(O)=O)c1ccccc1

Benzeneacetic acid alpha-hydroxy-

(-20℃)

With Ice Pack

≥ 2 years