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Y0001285

Sertraline impurity E

European Pharmacopoeia (EP) Reference Standard

Synonyme(s) :

(R)-(−)-Mandelic acid, (R)-α-Hydroxyphenylacetic acid

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About This Item

Formule linéaire :
C6H5CH(OH)CO2H
Numéro CAS:
611-71-2
Poids moléculaire :
152.15
Numéro Beilstein :
2691094
Numéro MDL:
MFCD00064251
Code UNSPSC :
41116107
ID de substance PubChem :
329831342
Nomenclature NACRES :
NA.24

Qualité

pharmaceutical primary standard

Famille d'API

sertraline

Fabricant/nom de marque

EDQM

Pf

131-133 °C (lit.)

Application(s)

pharmaceutical (small molecule)

Format

neat

Température de stockage

2-8°C

Chaîne SMILES 

O[C@@H](C(O)=O)c1ccccc1

InChI

1S/C8H8O3/c9-7(8(10)11)6-4-2-1-3-5-6/h1-5,7,9H,(H,10,11)/t7-/m1/s1

Clé InChI

IWYDHOAUDWTVEP-SSDOTTSWSA-N

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Description générale

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the Issuing Pharmacopoeia. For further information and support please go to the website of the issuing Pharmacopoeia.

Application

Sertraline impurity E EP Reference standard, intended for use in laboratory tests only as specifically prescribed in the European Pharmacopoeia.

Conditionnement

The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity, please visit the EDQM reference substance catalogue.

Autres remarques

Sales restrictions may apply.

Produit(s) apparenté(s)

Réf. du produit
Description
Tarif

Y0000867

Sertraline for system suitability, European Pharmacopoeia (EP) Reference Standard

Y0000866

Sertraline for peak identification, European Pharmacopoeia (EP) Reference Standard

1612539

Sertraline hydrochloride, United States Pharmacopeia (USP) Reference Standard

Y0000828

Sertraline hydrochloride, European Pharmacopoeia (EP) Reference Standard

1612517

Sertraline hydrochloride racemic mixture, United States Pharmacopeia (USP) Reference Standard

1612528

Sertraline hydrochloride Related Compound A, United States Pharmacopeia (USP) Reference Standard

BP883

Sertraline hydrochloride, British Pharmacopoeia (BP) Reference Standard

BP897

Sertraline hydrochloride impurity standard, British Pharmacopoeia (BP) Reference Standard

PHR2535

Sertraline hydrochloride, Pharmaceutical Secondary Standard; Certified Reference Material

Pictogrammes

Corrosion
GHS05

Mention d'avertissement

Danger

Mentions de danger

H318

Classification des risques

Eye Dam. 1

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

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Certificats d'analyse (COA)

Lot/Batch Number

Désolés, nous n'avons pas de COA pour ce produit disponible en ligne pour le moment.

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Selahattin Bozkurt et al.
Chirality, 24(2), 129-136 (2011-12-20)
Novel chiral calix[4]arene derivatives bearing amino alcohol moieties at the lower rim have been synthesized from the reaction of p-tert-butylcalix[4]arene diester with various amino alcohols. The transport of amino acid esters (phenylglycine, phenylalanine, and tryptophan methyl esters hydrochloride) and mandelic
M Monier et al.
International journal of biological macromolecules, 55, 207-213 (2013-01-30)
An enantioselective S-mandelic acid (S-MA) imprinted chitosan (SMIC) was prepared by cross-linking of chitosan using formaldehyde cross-linker, in the presence of S-MA as an imprint template molecule and 0.5% acetic acid solution as a solvent. Non-imprinted cross-linked chitosan (NIC) as
Jiao-Jiao Shangguan et al.
Applied biochemistry and biotechnology, 168(7), 1820-1833 (2012-10-12)
A 1,080-bp cDNA (CGMCC 2873) encoding of a cold-active lipase of Aspergillus fumigatus (AFL67) was cloned and expressed in Escherichia coli for the first time. The new lipase, AFL67, was one-step purified by 8.30 folds through Ni-NTA affinity chromatography with
Tsuyoshi Mita et al.
The Journal of organic chemistry, 77(5), 2159-2168 (2012-02-01)
Incorporation reactions of carbon dioxide (CO(2)) with N-Boc-α-amido and α-acetoxy stannanes were developed using CsF as a mild tin activator. Monoprotected α-amido stannanes could be used, and the corresponding arylglycine derivatives were obtained in moderate-to-high yields under 1 MPa (10
Shimin Mao et al.
Journal of separation science, 35(17), 2273-2281 (2012-07-19)
Resolution of racemic mandelic acid ((R,S)-MA) and numerical determination of binary competitive isotherm of (R,S)-MA on Chiralcel-OD column have been investigated in this study. The effects of the alcohol modifier and acidic additive in the mobile phase on the retention
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