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2-Hydroxy-2-phenylacetic acid Sale

(Synonyms: 扁桃酸,(±)-Mandelic acid; DL-Mandelic acid) 目录号 : GC38281

2-羟基-2-苯乙酸((±)-2-羟基-2-苯乙酸)是一种α-羟基羧酸,已广泛用作医药和精细化学品的中间体。

2-Hydroxy-2-phenylacetic acid Chemical Structure

Cas No.:90-64-2

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Sample solution is provided at 25 µL, 10mM.

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产品描述

2-Hydroxy-2-phenylacetic acid is an endogenous metabolite.

Chemical Properties

Cas No. 90-64-2 SDF
别名 扁桃酸,(±)-Mandelic acid; DL-Mandelic acid
Canonical SMILES C1=CC=CC=C1C(C(O)=O)O
分子式 C8H8O3 分子量 152.15
溶解度 Soluble in DMSO 储存条件 Store at -20°C
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溶解性数据

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1 mg 5 mg 10 mg
1 mM 6.5725 mL 32.8623 mL 65.7246 mL
5 mM 1.3145 mL 6.5725 mL 13.1449 mL
10 mM 0.6572 mL 3.2862 mL 6.5725 mL
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Research Update

Chirality Detection Using Nematic Liquid Crystal Droplets on Anisotropic Surfaces

Langmuir 2016 Jun 21;32(24):6140-7.PMID:27244587DOI:10.1021/acs.langmuir.6b00382.

Nematic liquid crystals (NLCs) form helical macroscopic structures through chiral induction when doped with chiral species. We describe a very simple, though highly sensitive method for determination of handedness and pitch of the induced twist in the case of very weak twisting powers of such chiral dopants. A tiny drop-typically less than 10 nL-of the chiral doped NLC is placed on a plate promoting a uniform planar surface anchoring of the liquid crystal director. At the curved NLC-air interface the anchoring is homeotropic and in the sessile droplets we get a locally twisted hybrid director structure with a disclination line extending across the droplet. The configuration of the disclination line (S-like or backwards S-like) reveals the sign of twisting power and extremely large pitch values in the range of 10 mm can easily be measured. We demonstrate the method using the standard NLC 4-cyano-4'-pentylbiphenyl (5CB), weakly doped with the chiral material 2-Hydroxy-2-phenylacetic acid (mandelic acid).

[Biotransformation of zipeprol (Mirsol) in humans. Gas chromatographic/mass spectrometric studies, using ammonia as a selective reactant gas (author's transl)]

J Clin Chem Clin Biochem 1981 Jan;19(1):25-30.PMID:7205156doi

After oral application of Zipeprol (Mirsol) the unchanged drug and nine degradation products were detected in human urine; six of them could be identified. All identified metabolites were detected in the alkaline urine fraction; after acid hydrolysis N-(2-hydroxyethyl)-piperazine was found as an artifact. With respect to the presented results, biotransformation of Zipeprol in man mainly follows three degradation routes: 1. alpha-cleavage leading to metabolite M4; 2. cleavage of the exocyclic N-C-bond of the piperazine ring leading to metabolites M3, M5, M6; 3. benzylic cleavage leading to benzylalcohol (M1); oxidation leading to 2-Hydroxy-2-phenylacetic acid (mandelic acid, M2).