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Catalog Number:
32430
CAS Number:
14152-97-7
2,3,4,6-Tetra-O-acetyl-ॆ-D-glucopyranosyl isothiocyanate for chiral derivatization
Purity:
≥ 99% (HPLC)
Synonym(s):
GITC
Documents
$88.63 /100MG
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Product Information

2,3,4,6-Tetra-O-acetyl-b-D-glucopyranosyl isothiocyanate is a versatile compound widely utilized in chiral derivatization processes, making it invaluable for researchers in the fields of organic chemistry and pharmaceuticals. This compound serves as a chiral reagent, enabling the differentiation of enantiomers in various analytical applications, particularly in chromatography. Its unique structure, featuring multiple acetyl groups, enhances its stability and solubility, facilitating easier handling and application in laboratory settings.

Moreover, this compound is recognized for its effectiveness in synthesizing complex molecules, which is crucial in drug development and the production of fine chemicals. Its ability to selectively react with amines and alcohols allows for the formation of stable derivatives, streamlining the identification and quantification of chiral compounds. Researchers can leverage 2,3,4,6-Tetra-O-acetyl-b-D-glucopyranosyl isothiocyanate to improve the efficiency of their workflows, ultimately leading to more accurate results in their studies.

Synonyms
GITC
CAS Number
14152-97-7
Purity
≥ 99% (HPLC)
Molecular Formula
C15H19NO9S
Molecular Weight
389.38
MDL Number
MFCD00043085
PubChem ID
312833
Melting Point
114 - 116 °C
Appearance
White powder
Optical Rotation
[a]20/D= -2 to -5 ° (C=1 in methylene chloride)
Conditions
Store at 2 - 8 °C
General Information
Synonyms
GITC
CAS Number
14152-97-7
Purity
≥ 99% (HPLC)
Molecular Formula
C15H19NO9S
Molecular Weight
389.38
MDL Number
MFCD00043085
PubChem ID
312833
Melting Point
114 - 116 °C
Appearance
White powder
Optical Rotation
[a]20/D= -2 to -5 ° (C=1 in methylene chloride)
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2,3,4,6-Tetra-O-acetyl-b-D-glucopyranosyl isothiocyanate is widely utilized in research focused on:

  • Chiral Derivatization: This compound is essential in the field of chiral chromatography, helping researchers separate and analyze enantiomers effectively, which is crucial in pharmaceuticals for drug development.
  • Biochemical Research: It serves as a valuable reagent in synthesizing glycosyl isothiocyanates, which can be used to study carbohydrate-protein interactions, aiding in the understanding of biological processes.
  • Drug Development: The compound is used in the modification of drug candidates to enhance their solubility and bioavailability, making it a key player in the pharmaceutical industry.
  • Food Industry: It can be applied in food chemistry to analyze glycosylated compounds, contributing to the development of healthier food products with improved nutritional profiles.
  • Environmental Science: This chemical is utilized in the detection of certain pollutants, helping researchers develop methods for monitoring and mitigating environmental contamination.

Citations