Cas no 29390-67-8 (6-Monodeoxy-6-monoamino-beta-cyclodextrine)

6-Monodeoxy-6-monoamino-beta-cyclodextrine structure
29390-67-8 structure
Product Name:6-Monodeoxy-6-monoamino-beta-cyclodextrine
CAS No:29390-67-8
MF:C42H71NO34
MW:1134
MDL:MFCD03452964
CID:239351
PubChem ID:9854967
Update Time:2025-11-01

6-Monodeoxy-6-monoamino-beta-cyclodextrine Chemical and Physical Properties

Names and Identifiers

    • b-Cyclodextrin, 6A-amino-6A-deoxy-
    • Mono-6-Amino-6-deoxy-beta-Cyclodextrin
    • mono-6-amino-mono-6-deoxy-β-CD
    • 6-Amino-6-deoxycyclomaltoheptaose
    • 6-Deoxy-6-amino-beta-cyclodextrin
    • 6-Monoamino-6-monodeoxy-beta-cyclodextrin
    • 6-Monoamino-beta-cyclodextrin
    • 6-Monodeoxy-6-monoamino-beta-cyclodextrin
    • Mono(6-amino-6-deoxy)-beta-cyclodextrin
    • CID 134691995
    • 6(I)-amino-6(I)-deoxycyclomaltoheptaose
    • 6-Monodeoxy-6-monoamino-beta-cyclodextrine
    • 6-AMino-6-deoxy -cyclodextrin
    • Mono-(6-amino-6-deoxy)-β-cyclodextrin
    • Mono-(6-amino-6-deoxy)-2-cyclodextrin
    • 6-Monodeoxy-6-MonoaMino-β-cyclodextrine
    • 6-Monoamino-b-cyclodextrin
    • beta-Cyclodextrin, 6A-amino-6A-deoxy-
    • Mono-(6-amino-6-deoxy)-A-cyclodextrin
    • AS-61686
    • CS-0187528
    • C74508
    • AKOS037645604
    • Mono-(6-Amino-6-deoxy)-Beta-cyclodextrin
    • 29390-67-8
    • MDL: MFCD03452964
    • Inchi: 1S/C42H71NO34/c43-1-8-29-15(50)22(57)36(64-8)72-30-9(2-44)66-38(24(59)17(30)52)74-32-11(4-46)68-40(26(61)19(32)54)76-34-13(6-48)70-42(28(63)21(34)56)77-35-14(7-49)69-41(27(62)20(35)55)75-33-12(5-47)67-39(25(60)18(33)53)73-31-10(3-45)65-37(71-29)23(58)16(31)51/h8-42,44-63H,1-7,43H2/t8-,9+,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+/m1/s1
    • InChI Key: OZBFLQITCMCIOY-DPWLHOGPSA-N
    • SMILES: O1[C@]2([H])[C@@]([H])([C@]([H])([C@@]([H])([C@@]([H])(C([H])([H])O[H])O2)O[C@]2([H])[C@@]([H])([C@]([H])([C@@]([H])([C@@]([H])(C([H])([H])O[H])O2)O[C@@]2([H])[C@]([H])([C@@]([H])([C@]([H])([C@]([H])(C([H])([H])O[H])O2)O[C@@]2([H])[C@]([H])([C@@]([H])([C@]([H])([C@]([H])(C([H])([H])O[H])O2)O[C@@]2([H])[C@]([H])([C@@]([H])([C@]([H])([C@]([H])(C([H])([H])O[H])O2)O[C@@]2([H])[C@]([H])([C@@]([H])([C@]([H])([C@]([H])(C([H])([H])O[H])O2)O[C@]2([H])[C@@]([H])([C@]([H])([C@@]1([H])[C@@]([H])(C([H])([H])N([H])[H])O2)O[H])O[H])O[H])O[H])O[H])O[H])O[H])O[H])O[H])O[H])O[H])O[H])O[H])O[H]

Computed Properties

  • Exact Mass: 1133.3857483g/mol
  • Monoisotopic Mass: 1133.3857483g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 21
  • Hydrogen Bond Acceptor Count: 35
  • Heavy Atom Count: 77
  • Rotatable Bond Count: 7
  • Complexity: 1840
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 35
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 560
  • Hydrogen Bond Acceptor Count: 35
  • Topological Polar Surface Area: 560A^2
  • Isotope Atom Count: 0
  • XLogP3: -15.3

Experimental Properties

  • Density: 1.608±0.06 g/cm3 (20 oC 760 Torr),
  • Melting Point: 260-265 oC
  • Boiling Point: 1527.8±60.0°C at 760 mmHg
  • Solubility: Soluble in water, DMF, DMSO.Insoluble in acetone, methanol, chloroform.
  • PSA: 559.84000
  • LogP: -14.56390
  • pka: 12.57±0.70(Predicted)

6-Monodeoxy-6-monoamino-beta-cyclodextrine Security Information

6-Monodeoxy-6-monoamino-beta-cyclodextrine Customs Data

  • HS CODE:9999999999

6-Monodeoxy-6-monoamino-beta-cyclodextrine Pricemore >>

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6-Monodeoxy-6-monoamino-beta-cyclodextrine Related Literature

Additional information on 6-Monodeoxy-6-monoamino-beta-cyclodextrine

Recent Advances in the Study of 6-Monodeoxy-6-monoamino-beta-cyclodextrine (CAS: 29390-67-8) and Its Applications in Chemical Biology and Medicine

In recent years, the compound 6-Monodeoxy-6-monoamino-beta-cyclodextrine (CAS: 29390-67-8) has garnered significant attention in the fields of chemical biology and pharmaceutical research. This modified cyclodextrin derivative, characterized by its unique structural properties, has shown promising potential in drug delivery, molecular recognition, and enzyme mimicry. The following research brief synthesizes the latest findings on this compound, highlighting its synthesis, characterization, and applications in therapeutic and diagnostic contexts.

The primary focus of recent studies has been on optimizing the synthesis of 6-Monodeoxy-6-monoamino-beta-cyclodextrine to improve yield and purity. Advanced techniques such as high-performance liquid chromatography (HPLC) and nuclear magnetic resonance (NMR) spectroscopy have been employed to characterize its structural integrity. Researchers have reported successful modifications to the amino group, enabling enhanced binding affinity for various guest molecules, including pharmaceutical compounds and biomolecules.

One of the most notable applications of 6-Monodeoxy-6-monoamino-beta-cyclodextrine is its role in drug delivery systems. Its ability to form inclusion complexes with hydrophobic drugs has been leveraged to improve solubility, stability, and bioavailability. Recent in vitro and in vivo studies have demonstrated its efficacy in delivering anticancer agents, such as doxorubicin, with reduced systemic toxicity. Additionally, its biocompatibility and low immunogenicity make it an attractive candidate for targeted drug delivery.

Beyond drug delivery, this compound has shown potential in molecular recognition and biosensing. Its cavity structure allows for selective binding to specific analytes, facilitating the development of sensitive and selective biosensors. Recent work has explored its use in detecting biomarkers for diseases such as cancer and neurodegenerative disorders. The integration of 6-Monodeoxy-6-monoamino-beta-cyclodextrine into electrochemical and optical sensing platforms has yielded promising results, with enhanced sensitivity and specificity.

In conclusion, 6-Monodeoxy-6-monoamino-beta-cyclodextrine (CAS: 29390-67-8) represents a versatile tool in chemical biology and medicine. Its unique properties and wide-ranging applications underscore its potential to address current challenges in drug delivery, diagnostics, and therapeutics. Future research should focus on scaling up synthesis, optimizing functionalization, and exploring novel applications in personalized medicine and nanotechnology.

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