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Merck
모든 사진(1)

주요 문서

779334

Sigma-Aldrich

β-Cyclodextrin

Wacker Chemie AG, ≥98.0% (HPLC)

동의어(들):

Cavamax® W7 Pharma, beta-Cyclodextrin, Caraway, Cycloheptaamylose, Cyclomaltoheptaose, Schardinger β-Dextrin

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About This Item

실험식(Hill 표기법):
C42H70O35
CAS Number:
Molecular Weight:
1134.98
Beilstein:
78623
EC Number:
MDL number:
UNSPSC 코드:
12352005
PubChem Substance ID:
NACRES:
NA.22

Quality Level

분석

≥98.0% (HPLC)

양식

powder

광학 활성

[α]/D 160 to 164°
[α]20/D +162±3°, c = 1.5% in H2O

제조업체/상표

Wacker Chemie AG

불순물

≤0.2% reducing substances
≤0.25% α- and γ-cyclodextrin (each)
≤0.5% related substances
≤5 ppm heavy metals
≤5 ppm residual solvents

무기 잔류물

≤0.10%

손실

≤14.0% loss on drying

pH

5.0-8.0 (1% in solution)

mp

290-300 °C (dec.) (lit.)

solubility

solution: 1%, clear

흡수

≤0.05 at 350-750 nm in solution at 1%
≤0.1 at 230-350 nm in solution at 1%

적합성

corresponds for identity

작용기

ether
hydroxyl

SMILES string

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]1[C@H](O)[C@H]2O

InChI

1S/C42H70O35/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/h8-63H,1-7H2/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

WHGYBXFWUBPSRW-FOUAGVGXSA-N

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애플리케이션

For R&D use

법적 정보

Cavasol is a registered trademark of Wacker Chemie AG

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


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문서 라이브러리 방문

Magdalena Ceborska et al.
Carbohydrate polymers, 97(2), 546-550 (2013-08-06)
Isopulegol, an insoluble in water and highly volatile compound, due to its neuroactive properties is a potentially important agent for medical applications. Formation of "host-guest" molecular complexes with cyclodextrins would lead to the increase of its water solubility and bioavailability.
Mayur Sangwai et al.
International journal of pharmaceutics, 453(2), 423-432 (2012-09-01)
Despite of advancements in dosage form design and use of multifunctional excipients, improvement in dissolution characteristics of molecules like Telmisartan (TEL) having exceedingly pH dependent and poor solubility profile is still challenging. The present research work explores an innovative particle
Shuye Wang et al.
Journal of chromatography. A, 1277, 84-92 (2013-01-12)
Methoxyethylamine monosubstituted β-cyclodextrin, mono-6(A)-(2-methoxyethyl-1-ammonium)-6(A)-β-cyclodextrin chloride (MEtAMCD), is synthesized and analytically characterized. Bearing a methoxy group in cyclodextrin rim, MEtAMCD exhibits outstanding enantioselectivities toward ampholytic and acidic racemates in capillary electrophoresis. Driven by inclusion complexation, electrostatic interactions and/or hydrogen bonding, the
Xu Zhang et al.
Chemical communications (Cambridge, England), 49(8), 825-827 (2012-12-14)
This work revealed that β-cyclodextrin was attached onto the surface of TiO(2) predominately by its secondary ring side, which caused paradoxical functions of β-cyclodextrin in the photodegradation of the four bisphenols. The equilibrium between the guest adsorbed through β-cyclodextrin onto
L Siman et al.
Physical review letters, 109(24), 248103-248103 (2013-02-02)
Binding of ligands to DNA can be studied by measuring the change of the persistence length of the complex formed, in single-molecule assays. We propose a methodology for persistence length data analysis based on a quenched disorder statistical model and

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