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Catalog Number:
27761
CAS Number:
6 de abril de 1987
Tetraacetato de 1-tio-β-D-glucosa
Purity:
≥ 99% (ensayo)
Synonym(s):
2,3,4,6-Tetra- O -acetil-1-tio-β-D-glucopiranosa
Temperature Sensitive
Documents
$40.30 /250 mg
Tamaño
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Product Information

1-Thio-b-D-glucose tetraacetate is a versatile compound that serves as a valuable tool in various biochemical and pharmaceutical applications. This thio derivative of glucose is characterized by its unique structure, which includes multiple acetyl groups that enhance its solubility and reactivity. Researchers often utilize this compound in glycosylation reactions, where it acts as a glycosyl donor, facilitating the synthesis of complex carbohydrates and glycoconjugates. Its ability to participate in selective reactions makes it particularly useful in the development of glycosylated drugs and biologically active compounds.

In addition to its synthetic applications, 1-Thio-b-D-glucose tetraacetate is also employed in the study of carbohydrate metabolism and enzyme interactions. Its thio group can mimic natural substrates, allowing for the exploration of enzyme mechanisms and the design of inhibitors. This compound's stability and reactivity profile make it an excellent candidate for further research in medicinal chemistry and biochemistry, providing researchers with a reliable reagent for advancing their studies in carbohydrate chemistry.

Synonyms
2,3,4,6-Tetra- O -acetil-1-tio-β-D-glucopiranosa
CAS Number
6 de abril de 1987
Purity
≥ 99% (ensayo)
Molecular Formula
C14H20O9S
Molecular Weight
364.37
MDL Number
MFCD00063271
PubChem ID
153711
Melting Point
115 - 118 °C (Literatura)
Appearance
Polvo blanco
Optical Rotation
[a] D 20 = -3,4 ± 0,5º (C=1% en Dioxano después de 20h) D 20 = 6 ± 1 º (C=2,2 en Cloroformo)
Conditions
Conservar a ≤ -4 °C
General Information
Synonyms
2,3,4,6-Tetra- O -acetil-1-tio-β-D-glucopiranosa
CAS Number
6 de abril de 1987
Purity
≥ 99% (ensayo)
Molecular Formula
C14H20O9S
Molecular Weight
364.37
MDL Number
MFCD00063271
PubChem ID
153711
Melting Point
115 - 118 °C (Literatura)
Appearance
Polvo blanco
Optical Rotation
[a] D 20 = -3,4 ± 0,5º (C=1% en Dioxano después de 20h) D 20 = 6 ± 1 º (C=2,2 en Cloroformo)
Conditions
Conservar a ≤ -4 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

1-Thio-b-D-glucose tetraacetate is widely utilized in research focused on:

  • Biochemical Research: This compound serves as a valuable tool in studying carbohydrate metabolism and enzyme interactions, helping researchers understand cellular processes.
  • Drug Development: It is used in the synthesis of glycosylated compounds, which can enhance the efficacy of pharmaceuticals by improving their bioavailability and targeting specific biological pathways.
  • Analytical Chemistry: The compound acts as a derivatizing agent in chromatography, aiding in the separation and identification of various biomolecules, thus streamlining analytical processes.
  • Food Industry: It can be employed in the development of flavoring agents and sweeteners, providing a natural alternative to synthetic additives while maintaining desirable taste profiles.
  • Cosmetic Formulations: The compound is incorporated into skincare products for its potential antioxidant properties, offering benefits such as improved skin hydration and protection against oxidative stress.

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