90-64-2
90-64-2
Chemical Structure
Mandelic acid
Synonym(s): (±)-Mandelic acid; DL-Mandelic acid
- CAS No.: 90-64-2
- Formula:C8H8O3
- Molecular Weight:152.15
IUPAC Name: 2-hydroxy-2-phenylacetic acid
InChIKey: IWYDHOAUDWTVEP-UHFFFAOYSA-N
SMILES: C1=CC=CC=C1C(C(O)=O)O
Biological Activity: Mandelic acid ((±)-Mandelic acid), an alpha-hydroxycarboxylic acid, has been widely used as an intermediate of pharmaceutical and fine chemicals. Mandelic acid shows antimicrobial activity and has been used for the research of urinary tract infections and vaginal trichomoniasis. Mandelic acid exhibits high sperm-immobilizing activity and low vaginal irritation[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Mandelic acid | 99.92% | Mandelic acid ((±)-Mandelic acid), an alpha-hydroxycarboxylic acid, has been widely used as an intermediate of pharmaceutical and fine chemicals. Mandelic acid shows antimicrobial activity and has been used for the research of urinary tract infections and vaginal trichomoniasis. Mandelic acid exhibits high sperm-immobilizing activity and low vaginal irritation. | ||||||||||||||||||||
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Mandelic acid (Standard) | 99.84% | Mandelic acid (Standard) is the analytical standard of Mandelic acid. This product is intended for research and analytical applications. Mandelic acid ((±)-Mandelic acid), an alpha-hydroxycarboxylic acid, has been widely used as an intermediate of pharmaceutical and fine chemicals. Mandelic acid shows antimicrobial activity and has been used for the research of urinary tract infections and vaginal trichomoniasis. Mandelic acid exhibits high sperm-immobilizing activity and low vaginal irritation. | ||||||||||||||||||||
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Mandelic acid-2,3,4,5,6-d5 | 98.42% | Mandelic acid-2,3,4,5,6-d5 is the deuterium labeled Mandelic acid. Mandelic acid ((±)-Mandelic acid), an alpha-hydroxycarboxylic acid, has been widely used as an intermediate of pharmaceutical and fine chemicals. Mandelic acid shows antimicrobial activity and has been used for the research of urinary tract infections and vaginal trichomoniasis. Mandelic acid exhibits high sperm-immobilizing activity and low vaginal irritation. | ||||||||||||||||||||
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Mandelic Acid-13C8 | 98.17% | Mandelic Acid-13C8 ((±)-Mandelic acid-13C8) is the 13C-labeled Mandelic acid (HY-W015591). Mandelic acid ((±)-Mandelic acid), an alpha-hydroxycarboxylic acid, has been widely used as an intermediate of pharmaceutical and fine chemicals. Mandelic acid shows antimicrobial activity and has been used for the research of urinary tract infections and vaginal trichomoniasis. Mandelic acid exhibits high sperm-immobilizing activity and low vaginal irritation. | ||||||||||||||||||||
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Thiomandelic acid | 95.37% | Thiomandelic acid is a broad spectrum inhibitor of Zinc -lactamases. | ||||||||||||||||||||
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D-(+)-Phenyllactic acid (Standard) | ≥98% | D-(+)-Phenyllactic acid (Standard) is the analytical standard of D-(+)-Phenyllactic acid. This product is intended for research and analytical applications. D-(+)-Phenyllactic acid is an anti-bacterial agent, excreted by Geotrichum candidum, inhibits a range of Gram-positive from humans and foodstuffs and Gram-negative bacteria found in humans. | ||||||||||||||||||||
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(S)-2-Hydroxy-3-phenylpropanoic acid (Standard) | ≥98% | (S)-2-Hydroxy-3-phenylpropanoic acid (Standard) is the analytical standard of (S)-2-Hydroxy-3-phenylpropanoic acid. This product is intended for research and analytical applications. (S)-2-Hydroxy-3-phenylpropanoic acid is the L-configuration of 2-Hydroxy-3-phenylpropanoic acid, and its level is closely related to some diseases, such as phenylketonuria. | ||||||||||||||||||||
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L-Phenylalanine-d5 | 99.96% | L-Phenylalanine-d5 is the deuterium labeled L-Phenylalanine. L-Phenylalanine ((S)-2-Amino-3-phenylpropionic acid) is an essential amino acid isolated from Escherichia coli. L-Phenylalanine is a α2δ subunit of voltage-dependent Ca+ channels antagonist with a Ki of 980 nM. L-phenylalanine is a competitive antagonist for the glycine- and glutamate-binding sites of N-methyl-D-aspartate receptors (NMDARs) (KB of 573 μM ) and non-NMDARs, respectively. L-Phenylalanine is widely used in the production of food flavors and pharmaceuticals. | ||||||||||||||||||||
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DL-Phenylalanine-d5 | 99.95% | DL-Phenylalanine-d5 is the deuterium labeled DL-Phenylalanine. | ||||||||||||||||||||
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Benzoic acid-d5 | 98.98% | Benzoic acid-d5 is a deuterium substitute for Benzoic acid. Benzoic acid is an aromatic alcohol that occurs naturally in many plants and is a common additive in food, beverages, cosmetics and other products. Benzoic acid can act as a preservative by inhibiting bacteria and fungi. | ||||||||||||||||||||
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trans-Cinnamic acid-d5 | 99.98% | trans-Cinnamic acid-d5 is the deuterium labeled trans-Cinnamic acid. trans-Cinnamic acid is a natural antimicrobial, with minimal inhibitory concentration (MIC) of 250 μg/mL against fish pathogen A. sobria, SY-AS1. | ||||||||||||||||||||
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2-Phenylglycine (Standard) | ≥98% | 2-Phenylglycine (Standard) is the analytical standard of 2-Phenylglycine (HY-W010248). This product is intended for research and analytical applications. 2-Phenylglycine (DL-α-Phenylglycine) is a metabolite in breast milk during the W2 to W4 lactation period. | ||||||||||||||||||||
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2-Phenylglycine-d5 | 99.01% | 2-Phenylglycine-d5 is the deuterium labeled 2-Phenylglycine. 2-Phenylglycine (DL-α-Phenylglycine) is a metabolite in breast milk during the W2 to W4 lactation period. | ||||||||||||||||||||
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H-D-Phg-OH | 99.99% | H-D-Phg-OH is a Glycine (HY-Y0966) derivative. | ||||||||||||||||||||
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D-α-Phenyl-glycine-d5 | 99.0% | D-α-Phenyl-glycine-d5 is the deuterium labeled D-α-Phenyl-glycine. | ||||||||||||||||||||
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Phenylglyoxylic acid-d5 | 99.90% | Phenylglyoxylic acid-d5 (Benzoylformic acid-d5) is a deuterium labeled Phenylglyoxylic acid (HY-W010255). Phenylglyoxylic acid (Benzoylformic acid) is a metabolite of ethylbenzene and styrene (EB/S) and can be used as a biomarker of exposure to EB/S in human. Phenylglyoxylic acid can be used as drug intermediate for synthesis of antineoplastic compounds. | ||||||||||||||||||||
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H-Phg-OH | 99.81% | H-Phg-OH is a Glycine (HY-Y0966) derivative. | ||||||||||||||||||||
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L-α-Phenyl-glycine-d5 | 98.0% | L-α-Phenyl-glycine-d5 is the deuterium labeled L-α-Phenyl-glycine. | ||||||||||||||||||||
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Tropic acid | 99.81% | Tropic acid (DL-Tropic acid) is an active small molecule that can be used as the pharmaceutical intermediate. | ||||||||||||||||||||
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D-Phenylalanine-d5 | 99.87% | D-Phenylalanine-d5 is the deuterium labeled D-Phenylalanine. D-Phenylalanine is the synthetic dextro isomer of phenylalanine. D-Phenylalanine inhibits biofilm development of Pseudoalteromonas sp. SC2014. | ||||||||||||||||||||
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D-(-)-Mandelic acid (Standard) | ≥98% | D-(-)-Mandelic acid (Standard) is the analytical standard of D-(-)-Mandelic acid. This product is intended for research and analytical applications. D-(-)-Mandelic acid is an orally active alpha hydroxycarboxylic acid that can be isolated from bitter almonds and Indian chestnut trees. It has antioxidant and antibacterial properties and is expected to play an important role in the treatment of rheumatoid arthritis. | ||||||||||||||||||||
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(S)-Mandelic acid | 99.75% | (S)-Mandelic Acid is a (S)-enantiomer of Mandelic Acid (HY-W015591). (S)-Mandelic Acid undergoes one-directional chiral inversion to (R)-Mandelic Acid in rat models. (S)-Mandelic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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Hydrocinnamic acid-d5 | 99.71% | Hydrocinnamic acid-d5 is the deuterium labeled Hydrocinnamic acid. Hydrocinnamic acid is the major rhizospheric compound with known growth regulatory activities. | ||||||||||||||||||||
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References
- [1]. Xia M, et al. dl-Mandelic acid exhibits high sperm-immobilizing activity and low vaginal irritation: A potential non-surfactant spermicide for contraception. Biomed Pharmacother. 2020;126:110104. [Content Brief]
- [2]. Tang LP, et al. DL-mandelic acid intercalated Zn-Al layered double hydroxide: A novel antimicrobial layered material. Colloids Surf B Biointerfaces. 2018;165:111-117. [Content Brief]
