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Merck
CN

389137

(2-Hydroxyethyl)-β-cyclodextrin

extent of labeling: ~0.7 mol per mol cellulose

Synonym(s):

2-HE-β-CD, 2-hydroxyethyl-β-CD, HP-β-CD

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About This Item

CAS Number:
128446-32-2
MDL number:
MFCD00074976
UNSPSC Code:
12352201
NACRES:
NA.22
Form:
powder

Key Documents

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InChI

1S/C84H154O56/c1-29(85)106-22-50-57-64(113-36(8)92)71(120-43(15)99)78(127-50)135-58-51(23-107-30(2)86)129-80(73(122-45(17)101)65(58)114-37(9)93)137-60-53(25-109-32(4)88)131-82(75(124-47(19)103)67(60)116-39(11)95)139-62-55(27-111-34(6)90)133-84(77(126-49(2

InChI key

TUOVZYHNLDIIMD-UHFFFAOYSA-N

SMILES string

O1C2OC(C(OC3OC(C(OC4OC(C(OC5OC(C(OC6OC(C(OC7OC(C(OC8OC(C1C(C8OC(O)C)OC(O)C)COC(O)C)C(C7OC(O)C)OC(O)C)COC(O)C)C(C6OC(O)C)OC(O)C)COC(O)C)C(C5OC(O)C)OC(O)C)COC(O)C)C(C4OC(O)C)OC(O)C)COC(O)C)C(C3OC(O)C)OC(O)C)COC(O)C)C(C2OC(O)C)OC(O)C)COC(O)C

form

powder

optical activity

[α]/D 120 to 150°, c = 1 in H2O

extent of labeling

~0.7 mol per mol cellulose

mp

260 °C (dec.) (lit.)

Quality Level

100

General description

(2-Hydroxyethyl)-β-cyclodextrin is a chemically modified, hydroxyalkylated derivative of cyclodextrin that finds potential use mainly in cosmetics application.

Application

(2-Hydroxyethyl)-β-cyclodextrin may be used as a chiral selector to resolve cathinone derivatives, lactic acid and oxybutynin enantiomers by capillary electrophoresis (CE), and high performance liquid chromatography (HPLC) techniques.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
MKCZ3577
MKCS7935
MKCN4726
MKCM1321
MKCF1407

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Design of Nanostructures for Versatile Therapeutic Applications
Pharmaceutical Nanotechnology (2018)
Cyclodextrin Fundamentals, Reactivity and Analysis
Environmental Chemistry for a Sustainable World (2018)
L Saavedra et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 766(2), 235-242 (2002-02-05)
The optimization of the separation conditions of the two optical isomers of lactic acid by a factorial design is reported. Initially, different chiral selectors were systematically investigated and then a experimental design with three quantitative factors (cyclodextrin concentration and background
Paweł Mateusz Nowak et al.
Electrophoresis, 39(19), 2406-2409 (2018-07-13)
Methcathinone (ephedrone), 4-methylmethcathinone (mephedrone), and 3-methylmethcathinone (metaphedrone) are toxicologically-important cathinone derivatives used commonly as designer drugs. In this work we show the first method allowing to separate simultaneously all these molecules in a chiral medium, ensuring good resolution between all
Equilibrium studies on enantioselective extraction of oxybutynin enantiomers by hydrophilic beta-cyclodextrin derivatives
Tang K, et al.
AIChE Journal, 57(11), 3027-3036 (2011)

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