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Merck
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Principaux documents

T5783

Supelco

2,3,4,6-Tetra-O-acetyl-β-D-glucopyranosyl isothiocyanate

for chiral derivatization, LiChropur, ≥98.0% (HPLC)

Synonyme(s) :

GITC

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About This Item

Formule empirique (notation de Hill):
C15H19NO9S
Numéro CAS:
Poids moléculaire :
389.38
Beilstein:
56699
Numéro MDL:
Code UNSPSC :
12000000
ID de substance PubChem :
Nomenclature NACRES :
NA.22

Qualité

for chiral derivatization
LiChropur

Niveau de qualité

Essai

≥98.0% (HPLC)

Technique(s)

HPLC: suitable

Pf

114-116 °C (lit.)

Température de stockage

2-8°C

Chaîne SMILES 

CC(=O)OC[C@H]1O[C@@H](N=C=S)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O

InChI

1S/C15H19NO9S/c1-7(17)21-5-11-12(22-8(2)18)13(23-9(3)19)14(24-10(4)20)15(25-11)16-6-26/h11-15H,5H2,1-4H3/t11-,12-,13+,14-,15-/m1/s1

Clé InChI

WOWNQYXIQWQJRJ-UXXRCYHCSA-N

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Description générale

2,3,4,6-Tetra-O-acetyl-β-D-glucopyranosyl isothiocyanate is a chiral derivatization reagent which reacts mainly with enantiomeric amino acids.

Application

Chiral reagent for resolution of amino acid derivatives.
GITC may have been used in the formation of diastereomers and for reversed-phase high-performance liquid chromatographic resolution of amino acid enantiomers.

Conditionnement

Bottomless glass bottle. Contents are inside inserted fused cone.

Produits recommandés

Discover LiChropur reagents ideal for HPLC or LC-MS analysis

Informations légales

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

Pictogrammes

Health hazardExclamation mark

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

Organes cibles

Respiratory system

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Les clients ont également consulté

Zhiqiong Chen et al.
Journal of separation science, 28(2), 193-196 (2005-03-10)
Chiral separation of racemic mixtures is of the greatest importance to the pharmaceutical industry, as the isomers of a given racemate may exhibit substantially different pharmacological effects, not to mention possibly differing toxicity behaviour. A novel chiral separation method is
J Gal et al.
Journal of pharmacological methods, 16(3), 261-269 (1986-11-01)
Many established and experimental adrenergic agonists are derivatives of 2-aminoethanol with a phenol or catechol moiety in the 1-position. There is considerable interest in the stereochemical aspects of the actions of such chiral drugs. Surprisingly, however, little has been published
X Li et al.
Journal of chromatography. B, Biomedical sciences and applications, 742(2), 433-439 (2000-07-20)
A reversed-phase high-performance liquid chromatographic method for the determination of the enantiomers of atenolol in rat hepatic microsome has been developed. Racemic atenolol was extracted from alkalinized rat hepatic microsome by ethyl acetate. The organic layer was dried with anhydrous
Sherry Wang et al.
Journal of pharmaceutical and biomedical analysis, 43(2), 701-707 (2006-09-09)
A stable isotopically labeled (SIL) analogue is believed to be the most appropriate internal standard in a quantitative bioanalytical liquid chromatography/tandem mass spectrometry (LC/MS/MS) assay. It is assumed that a SIL internal standard always compensates for variability in chemical derivatization
Klaas E A Max et al.
Proceedings of the National Academy of Sciences of the United States of America, 115(23), E5334-E5343 (2018-05-20)
Circulating extracellular RNAs (exRNAs) have the potential to serve as biomarkers for a wide range of medical conditions. However, limitations in existing exRNA isolation methods and a lack of knowledge on parameters affecting exRNA variability in human samples may hinder

Protocoles

Enantiomeric analysis of neurotransmitters and pharmaceuticals carrying functional amino groups, ß-adrenergic blockers; penicillamine, mexiletine; fine chemicals such as 1-phenyl-2-aminoethanol.

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