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779008

Sigma-Aldrich

α-Cyclodextrin

Wacker Chemie AG, 98.0-101.0% cyclodextrin basis (HPLC)

Synonym(s):

Cavamax® W6 Pharma, alpha-Cyclodextrin, α-Schardinger dextrin, Cyclohexaamylose, Cyclomaltohexaose

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100 ML
₹5,808.00

₹5,808.00


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100 ML
₹5,808.00

About This Item

Empirical Formula (Hill Notation):
C36H60O30
CAS Number:
Molecular Weight:
972.84
Beilstein:
79627
EC Number:
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:
NACRES:
NA.22

₹5,808.00


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Quality Level

Assay

98.0-101.0% cyclodextrin basis (HPLC)

form

solid

optical activity

[α]/D 147.0 to 152.0° in H2O (USP)

manufacturer/tradename

Wacker Chemie AG

impurities

≤0.20% reducing substances
≤0.25% β- and γ-cyclodextrin (each)
≤0.5% related substances
≤20 ppm residual solvents
≤5 ppm heavy metals (USP)

ign. residue

≤0.10% (USP)

loss

≤10.0% loss on drying

pH

5.0-8.0 (1% in solution)

mp

>278 °C (dec.) (lit.)

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This Item
900665333786751073
assay

≥90% (CP)

assay

≥98% (CP)

assay

≥98% (CP)

assay

98% (CP)

technique(s)

mass spectrometry (MS): suitable

technique(s)

mass spectrometry (MS): suitable

technique(s)

mass spectrometry (MS): suitable

technique(s)

mass spectrometry (MS): suitable

mass shift

M+3

mass shift

M+3

mass shift

M+3

mass shift

M+3

isotopic purity

≥95 atom % D

isotopic purity

≥98 atom % D

isotopic purity

≥98 atom % D

isotopic purity

98 atom % D

form

powder

form

powder

form

powder

form

powder

storage temp.

−20°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

−20°C

Application

α-Cyclodextrin can be used:
  • As a ligand in the complexation of nonionic surfactants and polyethylene glycols. α-cyclodextrin shows strong interaction with the surfactants that contains no benzene group.[1]
  • To protect linoleic acid from oxidation.[2]
  • In the synthesis of binuclear copper(II) complexes with cyclodextrins, which can be further used as a template for the preparation of copper nanoparticles incorporated on mesoporous silica.[3]

Legal Information

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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J D Metzger
Plant physiology, 94(1), 151-156 (1990-09-01)
Field pennycress (Thlaspi arvense L.) is a winter annual weed with a cold requirement for stem elongation and flowering. The relative abilities of several native gibberellins (GAs) and GA-precursors to elicit stem growth were compared. Of the eight compounds tested
C
Sittig's Handbook of Pesticides and Agricultural Chemicals, 91-195 (2015)
J D Metzger
Plant physiology, 86(1), 237-240 (1988-01-01)
Petiole growth in Thlaspi arvense L. was stimulated when a basic 8 hour photoperiod (4.20 milliwatts per square centimeter) was extended with low intensity light (0.16 milliwatt per square centimeter) from incandescent lamps. The day length extension was effective only
Nadjimov et al.
Journal of plant growth regulation, 18(1), 45-48 (1999-11-30)
The round-leafed mutant cotton line L-501 developed fasciation of the upper stem when field grown in Central Asia. Fasciation co-segregated with the mutant gene for round leaves In.(l) Fasciation developed at the flowering stage, but removal of floral buds did
Yan-Dong Wang et al.
Biotechnology and applied biochemistry, 37(Pt 1), 39-43 (2003-02-13)
Some metabolic inhibitors, mevastatin (MVS), chlorocholine chloride (CCC), sodium pyrophosphate (NaPP) and D,L-glyceraldehyde (DLG), were respectively added into the suspension cultures of the yew Taxus chinensis var. mairei at the late phase of cell growth to study isopentenyl pyrophosphate (IPP)

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