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DL-Mandelic acid
CAS No. 90-64-2
DL-Mandelic acid( acidomandelico )
Catalog No. M19671 CAS No. 90-64-2
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.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 28 | In Stock |
|
| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | 27 | In Stock |
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Biological Information
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Product NameDL-Mandelic acid
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NoteResearch use only, not for human use.
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Brief DescriptionIt 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.
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DescriptionIt 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.
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In VitroMandelic 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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In Vivo——
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Synonymsacidomandelico
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PathwayProteasome/Ubiquitin
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TargetEndogenous Metabolite
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Recptorothers
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Research Area——
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Indication——
Chemical Information
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CAS Number90-64-2
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Formula Weight152.15
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Molecular FormulaC8H8O3
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Purity>98% (HPLC)
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SolubilityDMSO:10 mM
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SMILESOC(C(O)=O)c1ccccc1
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Chemical NameBenzeneacetic acid alpha-hydroxy-
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Strittmatter M Isenberg E Grauer M T et al. CSF substance P somatostatin and monoaminergic transmitter metabolites in patients with narcolepsy.[J]. Neuroscience Letters 1996 218(2):99-102.
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