Mono-(6-amino-6-deoxy)-β-cyclodextrin - ≥99% , CAS No.29390-67-8

CAS: 29390-67-8 Cat. No.: M303345 Peso molecular: 1134

GRADE & PURITY ≥99%

Synonyms

6-Amino-6-deoxycyclomaltoheptaose | 6-Monoamino-β-cyclodextrin | 6A-Amino-6A-deoxy-β-cyclodextrin | 6-Amino-6-deoxy-β-cyclodextrin

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Descripción general

6-Monodeoxy-6-monoamino-β-cyclodextrin hydrochloride has been used for capillary electrophoresis. It has been used in a study to demonstrate that covalently attached molecular adapters can alter the ion selectivity of the α-hemolysin pore.

Specifications

Sinónimos

6-Amino-6-deoxycyclomaltoheptaose | 6-Monoamino-β-cyclodextrin | 6A-Amino-6A-deoxy-β-cyclodextrin | 6-Amino-6-deoxy-β-cyclodextrin

Especificaciones y pureza

≥99%

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C, Argon charged

Enviado en

Wet ice

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Pureza

≥99%

Nombres e identificadores

• Pubchem Sid: 504764981
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504764981
• Sonrisas canónicas: C(C1C2C(C(C(O1)OC3C(OC(C(C3O)O)OC4C(OC(C(C4O)O)OC5C(OC(C(C5O)O)OC6C(OC(C(C6O)O)OC7C(OC(C(C7O)O)OC8C(OC(O2)C(C8O)O)CO)CO)CO)CO)CO)CO)O)O)N
• IUPAC Name: (1S,3R,5R,6S,8R,10R,11S,13R,15R,16S,18R,20R,21S,23R,25R,26S,28R,30R,31S,33R,35R,36R,37R,38R,39R,40R,41R,42R,43R,44R,45R,46R,47R,48R,49R)-5-(aminomethyl)-10,15,20,25,30,35-hexakis(hydroxymethyl)-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: OZBFLQITCMCIOY-FOUAGVGXSA-N
• 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
• Isómeros SMILES: C([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)CO)CO)CO)CO)CO)CO)O)O)N
• Peso molecular: 1134
• Reaxy-Rn: 10774942
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=10774942&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Clase: Organooxygen compounds
• Subclass: Carbohydrates and carbohydrate conjugates
• Intermediate Tree Nodes: Not available
• Direct Parent: Oligosaccharides
• Alternative Parents: Aminosaccharides Oxanes Secondary alcohols Polyols Oxacyclic compounds Acetals Primary alcohols Organopnictogen compounds Monoalkylamines Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteropolycyclic compounds
• Substituents: Oligosaccharide - Amino saccharide - Oxane - Secondary alcohol - Acetal - Oxacycle - Organoheterocyclic compound - Polyol - Organic nitrogen compound - Primary alcohol - Primary amine - Hydrocarbon derivative - Organonitrogen compound - Organopnictogen compound - Primary aliphatic amine - Amine - Alcohol - Aliphatic heteropolycyclic compound
• Descripción: 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

Propiedades químicas y físicas

• Sensibilidad: Air sensitive
• Peso molecular: 1134.000 g/mol
• XLogP3: -15.300
• Hydrogen Bond Donor Count: 21
• Hydrogen Bond Acceptor Count: 35
• Rotatable Bond Count: 7
• Exact Mass: 1133.39 Da
• Monoisotopic Mass: 1133.39 Da
• Topological Polar Surface Area: 560.000 Ų
• Heavy Atom Count: 77
• Formal Charge: 0
• Complexity: 1840.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 35
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referencias

1. Zhen Deng, Peiwen Yang, Long Ma, Gang Li, Yunhua Yu, Xiaoping Yang.  (2025)  Constructing interfacial pulleys with branched polynaphthalamic acid polyrotaxane: a new route to superior interfacial toughness and strength in carbon fiber-reinforced composites.  COMPOSITES PART B-ENGINEERING,      [PMID:] [10.1016/j.compositesb.2025.112597]

2. Yunfan Li, Kaiwen Bao, Renzheng Huan, Tian Wang, Ya Wang, Shuai Wu, Xin Chen, Jiashang Huang, Li Zhu, Jianshu Li, Haifeng Yang, Wei Wu.  (2026)  RAP-peptide functionalized biomimetic nanoformulation with pathological ROS/pH-responsive drug release for target immunotherapy in glioma.  JOURNAL OF NANOBIOTECHNOLOGY,      [PMID:41654805] [10.1186/s12951-026-04055-4]