(2-Hydroxypropyl)-β-cyclodextrin

ALDRICH/778907 - Produced by Wacker Chemie AG, Burghausen, Germany, Life Science

Synonym: Cavasol^® W7 HP

CAS Number: 128446-35-5
EC Number: 420-920-1
Product Type: Chemical

Catalog Number	PKG Qty.	Price	Quantity


45-778907-100G	100 g	$215.00 1/EA		Add To Favorites
45-778907-500G	500 g	$741.00 1/EA		Add To Favorites
45-778907-10KG	10 kg	$11880.00 1/EA		Add To Favorites

Properties
Descriptions
Safety Info.
Basic Data

conductivity	≤200 μS/cm (Ph Eur)
extent of labeling	0.59-0.73 molar substitution
form	powder
grade	Produced by Wacker Chemie AG, Burghausen, Germany, Life Science
impurities	≤0.1% related substances, any (Ph Eur)
	≤0.5% propylene glycol (Ph Eur)
	≤1.0% β-dex (Ph Eur)
	≤1.0% related substances, total other
	≤1.0 ppm propylene oxide
InChI	1S/C63H112O42/c1-22(64)8-85-15-29-50-36(71)43(78)57(92-29)100-51-30(16-86-9-23(2)65)94-59(45(80)38(51)73)102-53-32(18-88-11-25(4)67)96-61(47(82)40(53)75)104-55-34(20-90-13-27(6)69)98-63(49(84)42(55)77)105-56-35(21-91-14-28(7)70)97-62(48(83)41(56)76)103-54-33(19-89-12-26(5)68)95-60(46(81)39(54)74)101-52-31(17-87-10-24(3)66)93-58(99-50)44(79)37(52)72/h22-84H,8-21H2,1-7H3/t22?,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+,49+,50+,51+,52-,53-,54-,55-,56-,57+,58-,59+,60-,61-,62-,63-/m1/s1
InChI key	ODLHGICHYURWBS-RYJYQAAZSA-N
loss	≤10.0% loss on drying
SMILES string	CC(O)COCC1OC2OC3C(COCC(C)O)OC(OC4C(COCC(C)O)OC(OC5C(COCC(C)O)OC(OC6C(COCC(C)O)OC(OC7C(COCC(C)O)OC(OC8C(COCC(C)O)OC(OC1C(OCC(C)O)C2OCC(C)O)C(OCC(C)O)C8OCC(C)O)C(OCC(C)O)C7OCC(C)O)C(OCC(C)O)C6OCC(C)O)C(OCC(C)O)C5OCC(C)O)C(OCC(C)O)C4OCC(C)O)C(OCC(C)O)C3OCC(C)O
suitability	clear, colorless for appearance of solution
	positive for identity

Application:	(2-Hydroxypropyl)-β-cyclodextrin can be used: • In the preparation of imidazole nucleosides via enzymatic transglycosylation to improve the solubility and/or stability of 4-aryl and 4-heteroaryl-1H-imidazole reactants. • Cyanazine-hydroxypropyl-β-cyclodextrin inclusion complex with enhanced water solubility when compared to cyanazine.
Application:	The solubility of lipophilic drugs increases linearly with the concentration of hydroxypropyl-β-cyclodextrin (HBC) in aqueous solution because of the complex between HBC and the drug. This guest-host type complex is formed between the drug and the non-polar cavity in the HBC that results in enhanced solubility. Solutions may be lyophilized to produce freely soluble powders. Non-toxic in rabbits and mice.
Legal Information:	Cavasol is a registered trademark of Wacker Chemie AG

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point(F)	Not applicable
Flash Point(C)	Not applicable

UNSPSC

12352201

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