CAS 84216-71-7

(1S,3R,5R,6S,8R,10R,11S,13R,15R,16S,18R,20R,21S,23R,25R,26S,28R,30R,31S,33R,35R,36S,37R,38R,39R,40R,41R,42R,43R,44R,45R,46R,47R,48R,49R)-36,38,39,40,41,42,43,44,45,46,47,48,49-tridecahydroxy-5,10,15,20,25,30,35-heptakis(hydroxymethyl)-2,4,7,9,12,14,17,19,

Description:

The chemical substance with the name provided is a complex polyol, characterized by a highly branched structure featuring multiple hydroxyl (-OH) groups. This compound is notable for its extensive hydroxymethyl substitutions, which contribute to its hydrophilicity and potential solubility in water. The stereochemistry indicated by the numerous chiral centers suggests that the molecule may exhibit specific spatial configurations, influencing its biological activity and interactions. Such polyols are often investigated for their applications in pharmaceuticals, cosmetics, and as potential biomaterials due to their biocompatibility and ability to form hydrogen bonds. The presence of multiple hydroxyl groups can also enhance the compound's reactivity, making it suitable for further chemical modifications. Additionally, the molecular complexity implies that it may possess unique physical properties, such as viscosity and melting point, which are important for its practical applications. Overall, this substance exemplifies the intricate nature of organic compounds with significant implications in various scientific fields.

Formula: C₄₉H₇₆O₃₇S

InChI: InChI=1/C49H76O37S/c1-13-2-4-14(5-3-13)87(70,71)86-42-34(69)41-21(12-56)78-49(42)85-40-20(11-55)77-47(33(68)27(40)62)83-38-18(9-53)75-45(31(66)25(38)60)81-36-16(7-51)73-43(29(64)23(36)58)79-35-15(6-50)72-44(28(63)22(35)57)80-37-17(8-52)74-46(30(65)24(37)59)82-39-19(10-54)76-48(84-41)32(67)26(39)61/h2-5,15-69H,6-12H2,1H3/t15-,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-,49-/m1/s1

Synonyms:

• (1S,3R,5R,6S,8R,10R,11S,13R,15R,16S,18R,20R,21S,23R,25R,26S,28R,30R,31S,33R,35R,36S,37R,38R,39R,40R,41R,42R,43R,44R,45R,46R,47R,48R,49R)-36,38,39,40,41,42,43,44,45,46,47,48,49-Tridecahydroxy-5,10,15,20,25,30,35-heptakis(hydroxymethyl)-2,4,7,9,12,14,17,19,22,24,27,29,32,34-tetradecaoxaoctacyclo[31.2.2.23,6

Mono-2-O-(p-toluenesulfonyl)-β-cyclodextrin

CAS: 84216-71-7

Formula: C₄₉H₇₆O₃₇S

Purity: >97.0%(HPLC)

Color and Shape: White to Almost white powder to crystal

Molecular weight: 1,289.17

Ref: 3B-M1741

Mono-2-O-(p-toluenesulfonyl)-β-cyclodextrin

CAS: 84216-71-7

Formula: C₄₉H₇₆O₃₇S

Purity: 97%

Color and Shape: Solid

Molecular weight: 1289.1705

Ref: IN-DA003S59

Mono-2-O-(p-toluenesulfonyl)-b-cyclodextrin hydrate

CAS: 84216-71-7

This beta-cyclodextrin (β-CD) derivative is a functionalized cyclic oligosaccharide composed of seven glucose units, characterized by a hydrophilic exterior and a lipophilic cavity (bigger than α-CD and smaller than γ-CDs), which allows it to encapsulate various guest molecules. This structural feature facilitates its use in multiple applications, including pharmaceuticals, food enhancement, and cosmetics. In the pharmaceutical industry, it enhances the solubility and stability of poorly water-soluble drugs, improving their bioavailability and efficacy while also masking unpleasant tastes. The food sector utilizes it as a stabilizer for flavors, colors, and nutrients, extending shelf life by protecting sensitive ingredients from degradation. In cosmetics, it serves as a complexing agent for fragrances and active components, ensuring their stability and controlled release. Its use expands to many other fields, including nanotechnology for drug delivery systems, environmental remediation for extracting organic pollutants, textiles for slow-release fragrances, and analytical chemistry for chiral separation.

Formula: C₄₉H₇₆O₃₇S•(H₂O)x

Purity: Min. 97 Area-%

Color and Shape: Powder

Molecular weight: 1,289.17 g/mol

Ref: 3D-FM62119