Cyclodextrin HPB (HP-β-CD) - PharmPure™, USP , CAS No.128446-35-5

CAS: 128446-35-5 Cat. No.: C485578 EC Number: 603-269-8

GRADE & PURITY PharmPure™, USP

Synonyms

A-cyclodextrin (HP- | CCG-270688 | (2-Hydroxypropyl)- | HP-b-CDHydroxypropyl betadex | s4760 | HP-b-CD | AC-3234 | (2-Hydroxypropyl)-b-cyclodextrin | AKOS025212232 | AS-15255 | Hydroxypropyl-b-cyclodextrin | HMS3885J22 | A-cyclodextrin | A-CD) | (1R,3S,5S

Storage

Room temperature

Shipped In

Normal

Overview

(2-Hydroxypropyl)-β-cyclodextrin is the most widely used modified cyclodextrin. The compound has shown to change the physicochemical properties of lipophilic compounds when co-administered. (2-Hydroxypropyl)-β-cyclodextrin functions by forming an inclusion complex with the compound being administered for easier diffusion across biological membranes, and its popularity can be attributed to its large 7 glucose unit cavity size. Some advantageous effects are reduction of negative effects, increased aqueous solubility and increased stability. The effects of (2-Hydroxypropyl)-β-cyclodextrin have been observed to be dose dependent with both advantageous and disadvantageous results occurring at sporadic concentrations. The compound may also increase the antimicrobial effectiveness of chemical agents by increasing their release rate.
A cyclodextrin that allows easier diffusion of lipophiles across biological membranes

Specifications

Synonyms

A-cyclodextrin (HP- | CCG-270688 | (2-Hydroxypropyl)- | HP-b-CDHydroxypropyl betadex | s4760 | HP-b-CD | AC-3234 | (2-Hydroxypropyl)-b-cyclodextrin | AKOS025212232 | AS-15255 | Hydroxypropyl-b-cyclodextrin | HMS3885J22 | A-cyclodextrin | A-CD) | (1R,3S,5S

Specifications & Purity

PharmPure™, USP

Storage

Room temperature

Shipped In

Normal

Grade

PharmPure™, USP

Names and Identifiers

• Pubchem Sid: 504771528
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504771528
• Canonical Smiles: CC(O)COCC1OC2OC3C(COCC(C)O)OC(OC4C(COCC(C)O)OC(OC5C(COCC(C)O)OC(OC6C(COCC(C)O)OC(OC7C(COCC(C)O)OC(OC8C(COCC(C)O)OC(OC1C(OCC(C)O)C2OCC(C)O)C(OCC(C)O)C8OCC(C)O)C(OCC(C)O)C7OCC(C)O)C(OCC(C)O)C6OCC(C)O)C(OCC(C)O)C5OCC(C)O)C(OCC(C)O)C4OCC(C)O)C(OCC(C)O)C3OCC(C)O
• IUPAC Name: (1R,3S,5S,6R,8S,10S,11R,13S,15S,16R,18S,20S,21R,23S,25S,26R,28S,30S,31R,33S,35S,36S,37S,38S,39S,40S,41S,42S,43S,44S,45S,46S,47S,48S,49S)-5,10,15,20,25,30,35-heptakis(2-hydroxypropoxymethyl)-2,4,7,9,12,14,17,19,22,24,27,29,32,34-tetradecaoxaoctacyclo[31.2.2.23,6.28,11.213,16.218,21.223,26.228,31]nonatetracontane-36,37,38,39,40,41,42,43,44,45,46,47,48,49-tetradecol
• InChIKey: ODLHGICHYURWBS-FOSILIAISA-N
• INCHI: 1S/C63H112O42/c1-22(64)8-85-15-29-50-36(71)43(78)57(92-29)100-51-30(16-86-9-23(2)65)94-59(45(80)38(51)73)102-53-32(18-88-11-25(4)67)96-61(47(82)40(53)75)104-55-34(20-90-13-27(6)69)98-63(49(84)42(55)77)105-56-35(21-91-14-28(7)70)97-62(48(83)41(56)76)103-54-33(19-89-12-26(5)68)95-60(46(81)39(54)74)101-52-31(17-87-10-24(3)66)93-58(99-50)44(79)37(52)72/h22-84H,8-21H2,1-7H3/t22?,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-,50-,51-,52-,53-,54-,55-,56-,57-,58-,59-,60-,61-,62-,63-/m0/s1
• Isomeric SMILES: CC(COC[C@H]1[C@H]2[C@H]([C@@H]([C@@H](O1)O[C@H]3[C@@H](O[C@H]([C@H]([C@@H]3O)O)O[C@H]4[C@@H](O[C@H]([C@H]([C@@H]4O)O)O[C@H]5[C@@H](O[C@H]([C@H]([C@@H]5O)O)O[C@H]6[C@@H](O[C@H]([C@H]([C@@H]6O)O)O[C@H]7[C@@H](O[C@H]([C@H]([C@@H]7O)O)O[C@H]8[C@@H](O[C@@H](O2)[C@H]([C@@H]8O)O)COCC(C)O)COCC(C)O)COCC(C)O)COCC(C)O)COCC(C)O)COCC(C)O)O)O)O
• WGK Germany: 3
• Alternate CAS: 94035-02-6

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Class Organooxygen compounds
      • Subclass Carbohydrates and carbohydrate conjugates

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Class: Organooxygen compounds
• Subclass: Carbohydrates and carbohydrate conjugates
• Intermediate Tree Nodes: Not available
• Direct Parent: Oligosaccharides
• Alternative Parents: Oxanes Secondary alcohols Polyols Oxacyclic compounds Dialkyl ethers Acetals Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteropolycyclic compounds
• Substituents: Oligosaccharide - Oxane - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Polyol - Ether - Dialkyl ether - Acetal - Hydrocarbon derivative - Alcohol - Aliphatic heteropolycyclic compound
• Description: This compound belongs to the class of organic compounds known as oligosaccharides. These are carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Solubility: 450g/L
• Molecular Weight: 1541.500 g/mol
• XLogP3: -13.000
• Hydrogen Bond Donor Count: 21
• Hydrogen Bond Acceptor Count: 42
• Rotatable Bond Count: 28
• Exact Mass: 1540.66 Da
• Monoisotopic Mass: 1540.66 Da
• Topological Polar Surface Area: 619.000 Ų
• Heavy Atom Count: 105
• Formal Charge: 0
• Complexity: 2010.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 35
• Undefined Atom Stereocenter Count: 7
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1