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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
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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Chao Ma et al.
Chirality, 23(5), 379-382 (2011-04-14)
This work reports the chiral separation of D,L-mandelic acid with cellulose membranes. Cellulose was chosen as membrane material because it possesses multichiral carbon atoms in its molecular structure unit. The flux and permselective properties of membrane using aqueous solutions of
Liang Jin et al.
Zeitschrift fur Naturforschung. C, Journal of biosciences, 66(9-10), 499-506 (2011-12-24)
To study the effects of mandelic acid (MA) on the brown planthopper (BPH), Nilaparvata lugens, the survival rate and behaviour of BPH fed on an artificial diet with different dosages of MA was observed. The survival rate of BPH decreased
Yubo Wu et al.
The Journal of organic chemistry, 76(14), 5685-5695 (2011-05-31)
We have prepared chiral fluorescent bisboronic acid sensors with 3,6-dithiophen-2-yl-9H-carbazole as the fluorophore. The thiophene moiety was used to extend the π-conjugation framework of the fluorophore in order to red-shift the fluorescence emission and, at the same time, to enhance
Zhoutong Sun et al.
Microbial cell factories, 10, 71-71 (2011-09-14)
Mandelic acid (MA), an important component in pharmaceutical syntheses, is currently produced exclusively via petrochemical processes. Growing concerns over the environment and fossil energy costs have inspired a quest to develop alternative routes to MA using renewable resources. Herein we
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
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