189307-64-0 Usage
Uses
Used in Research Applications:
3A-Amino-3A-deoxy-(2AS,3AS)-gamma-cyclodextrin Hydrate is used as a research compound for various purposes, including the study of host-guest interactions, molecular recognition, and drug delivery systems. Its unique structure allows it to form stable complexes with a wide range of guest molecules, making it an ideal candidate for investigating the properties and behavior of these interactions.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3A-Amino-3A-deoxy-(2AS,3AS)-gamma-cyclodextrin Hydrate is used as a carrier molecule for drug delivery systems. Its ability to form inclusion complexes with various drugs enhances the solubility, stability, and bioavailability of these compounds, leading to improved therapeutic outcomes.
Used in Food Industry:
3A-Amino-3A-deoxy-(2AS,3AS)-gamma-cyclodextrin Hydrate is also used in the food industry as a stabilizing and encapsulating agent. Its ability to form complexes with various flavors, colors, and other additives helps to improve the quality, shelf life, and sensory properties of food products.
Used in Environmental Applications:
In environmental applications, 3A-Amino-3A-deoxy-(2AS,3AS)-gamma-cyclodextrin Hydrate is used for the removal of pollutants and contaminants from water and soil. Its ability to form complexes with various toxic substances allows for efficient and selective removal, contributing to a cleaner and safer environment.
Used in Cosmetics Industry:
In the cosmetics industry, 3A-Amino-3A-deoxy-(2AS,3AS)-gamma-cyclodextrin Hydrate is used as an ingredient in various skincare and hair care products. Its ability to form complexes with active ingredients, such as antioxidants, vitamins, and essential oils, enhances their stability, penetration, and efficacy, leading to improved product performance and benefits for the user.
Check Digit Verification of cas no
The CAS Registry Mumber 189307-64-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,9,3,0 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 189307-64:
(8*1)+(7*8)+(6*9)+(5*3)+(4*0)+(3*7)+(2*6)+(1*4)=170
170 % 10 = 0
So 189307-64-0 is a valid CAS Registry Number.
InChI:InChI=1/C48H81NO39/c49-17-18(58)41-73-9(1-50)33(17)81-42-26(66)19(59)35(11(3-52)74-42)83-44-28(68)21(61)37(13(5-54)76-44)85-46-30(70)23(63)39(15(7-56)78-46)87-48-32(72)25(65)40(16(8-57)80-48)88-47-31(71)24(64)38(14(6-55)79-47)86-45-29(69)22(62)36(12(4-53)77-45)84-43-27(67)20(60)34(82-41)10(2-51)75-43/h9-48,50-72H,1-8,49H2/t9-,10-,11-,12-,13-,14-,15-,16-,17+,18+,19-,20-,21-,22-,23-,24-,25-,26-,27-,28-,29-,30-,31-,32-,33-,34-,35-,36-,37-,38-,39-,40-,41-,42-,43-,44-,45-,46-,47-,48-/m1/s1
189307-64-0Relevant articles and documents
Synthesis and characterisation of the 3-amino-derivative of γ-cyclodextrin, showing receptor ability and metal ion coordination properties
Contino, Annalinda,Cucinotta, Vincenzo,Giuffrida, Alessandro,Maccarrone, Giuseppe,Messina, Marianna,Puglisi, Antonino,Vecchio, Graziella
, p. 4765 - 4767 (2008)
The 3-hydroxy group of one glucopyranosinic ring of γ-cyclodextrin was selectively substituted with an amino moiety to obtain a new compound able to complex copper(II). Indeed, the new ligand, an altro-γ-CD, forms stable complexes with Cu(II), as the analogous 3-amino derivative β-CD previously exploited for the chiral separation of some amino acids by ligand exchange mechanism in capillary electrophoresis. Furthermore, the ligand forms a stable inclusion complex with anthraquinone-2-sulfonate.
