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Merck
CN

861413

γ-环糊精 水合物

别名:

γ-Schardinger dextrin, 环八淀粉

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关于此项目

经验公式(希尔记法):
C48H80O40 · xH2O
化学文摘社编号:
分子量:
1297.12 (anhydrous basis)
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352005
EC Number:
241-482-4
MDL number:
Form:
powder
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InChI key

SPKUKQHKKVTYOE-SMTXKKGASA-N

InChI

1S/C48H80O40.H2O/c49-1-9-33-17(57)25(65)41(73-9)82-34-10(2-50)75-43(27(67)19(34)59)84-36-12(4-52)77-45(29(69)21(36)61)86-38-14(6-54)79-47(31(71)23(38)63)88-40-16(8-56)80-48(32(72)24(40)64)87-39-15(7-55)78-46(30(70)22(39)62)85-37-13(5-53)76-44(28(68)20(37)60)83-35-11(3-51)74-42(81-33)26(66)18(35)58;/h9-72H,1-8H2;1H2/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

SMILES string

O.OC[C@H]1O[C@@H]2O[C@H]3[C@H](O)[C@@H](O)[C@H](O[C@@H]3CO)O[C@H]4[C@H](O)[C@@H](O)[C@H](O[C@@H]4CO)O[C@H]5[C@H](O)[C@@H](O)[C@H](O[C@@H]5CO)O[C@H]6[C@H](O)[C@@H](O)[C@H](O[C@@H]6CO)O[C@H]7[C@H](O)[C@@H](O)[C@H](O[C@@H]7CO)O[C@H]8[C@H](O)[C@@H](O)[C@H](O[C@@H]8CO)O[C@H]9[C@H](O)[C@@H](O)[C@H](O[C@@H]9CO)O[C@H]1[C@H](O)[C@H]2O

form

powder

optical activity

[α]20/D +176.1°, c = 1 in H2O (dried basis)

mp

267 °C (dec.) (lit.)

functional group

ether

Quality Level

General description

γ-cyclodextrin (γ-CD) is a water-soluble cyclic octamer of D-glucose units linked via α(1→4) glycosidic bonds. Its ability to form several inclusion complexes with organic as well as inorganic compounds makes it a potential candidate in solid and solution state determinations.

Application

用于评估暴露于药用辅料和杀微生物剂的生殖器上皮细胞活力、完整性和炎症实验的改性剂

用于研究α-、β-和γ-环糊精与二氯钒主客体相互作用的反应物
γ-Cyclodextrin hydrate may be used to form inclusion complexes with steviol glycosides, 1-propanol, tempone and di-tert-butyl nitroxide followed by their characterization by various analytical techniques.

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

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分析证书(COA)

Lot/Batch Number

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Spin-label-induced selective carbon-13 nuclear relaxation: structures of the. gamma.-cyclodextrin-tempone and. alpha.-cyclodextrin-di-tert-butyl nitroxide inclusion complexes in solution
Eastman MP, et al.
Macromolecules, 22(10), 3888-3892 (1989)
Mani Upreti et al.
International journal of molecular sciences, 12(11), 7529-7553 (2011-12-17)
Steviol glycosidesrebaudioside (reb) A, C and D have low aqueous solubilities. To improve their aqueous solubilities, inclusion complex of steviol glycosides, reb A, C and D and gamma cyclodextrin were prepared by freeze drying method and further characterized by means
R G Winkler et al.
Journal of computer-aided molecular design, 14(7), 659-667 (2000-09-29)
We study by molecular dynamics simulations the hydration of beta-cyclodextrin. Our simulations show that within these barrel-shaped molecules hydrophobicity dominates, while at the top and bottom sides of the barrel interactions with water are mostly hydrophilic in nature. These results
Determination of the impurity profile of gamma-cyclodextrin by high-performance liquid chromatography
White G, et al.
Journal of Chromatography A, 625(2), 157-161 (1992)
Structure of the gamma-cyclodextrin-1-propanol-17H2O inclusion complex
Ding J, et al.
Acta Crystallographica Section B, Structural Science, 47(5), 731-738 (1991)

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