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Catalog Number:
32352
CAS Number:
23739-88-0
Triacétyl-β-cyclodextrine
Purity:
≥ 98 % (HPLC)
Synonym(s):
Hénéicosaacétate de β-cyclodextrine
Documents
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Taille
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Product Information

Conserver à l'abri des agents oxydants forts, des sources d'inflammation.

Synonyms
Hénéicosaacétate de β-cyclodextrine
CAS Number
23739-88-0
Purity
≥ 98 % (HPLC)
Molecular Formula
C 84 H 112 O 56
Molecular Weight
2017.75
MDL Number
MFCD00074981
PubChem ID
16133039
Melting Point
204-206° C
Appearance
Poudre cristalline blanche
Optical Rotation
[a]25/D= 125 ± 4° (C=1 dans CHCl 3 )
Conditions
Conserver à l'abri des agents oxydants forts, des sources d'inflammation.
General Information
Synonyms
Hénéicosaacétate de β-cyclodextrine
CAS Number
23739-88-0
Purity
≥ 98 % (HPLC)
Molecular Formula
C 84 H 112 O 56
Molecular Weight
2017.75
MDL Number
MFCD00074981
PubChem ID
16133039
Melting Point
204-206° C
Appearance
Poudre cristalline blanche
Optical Rotation
[a]25/D= 125 ± 4° (C=1 dans CHCl 3 )
Conditions
Conserver à l'abri des agents oxydants forts, des sources d'inflammation.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Triacetyl-b-cyclodextrin is widely utilized in research focused on:

  • Pharmaceutical Formulations: It acts as a drug delivery agent, enhancing the solubility and stability of poorly soluble drugs, which can improve their bioavailability in the body.
  • Food Industry: This compound is used as a food additive to encapsulate flavors and nutrients, protecting them from degradation and enhancing their release during consumption.
  • Cosmetic Products: It serves as a stabilizer and carrier for active ingredients in cosmetics, ensuring that they remain effective and are delivered properly to the skin.
  • Environmental Applications: Triacetyl-b-cyclodextrin can be employed in the remediation of contaminated water by encapsulating pollutants, making them easier to remove from the environment.
  • Analytical Chemistry: It is utilized in chromatography as a chiral selector, helping to separate and analyze enantiomers in various chemical samples.

Citations