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. 2016 Dec 20;21(12):1748. doi: 10.3390/molecules21121748

Table 1.

Structure of native CDs and common modified CDs.

graphic file with name molecules-21-01748-i001.jpg
Abbreviation n Substituent (R) Number of R Group by CD
α-CD 6 (−) 0
β-CD 7 (−) 0
γ-CD 8 (−) 0
HPαCD 6 -CH2-CHOH-CH3 3.6
RAMEα 6 -CH3 10.8
HPβCD 7 -CH2-CHOH-CH3 5.6
KLEPTOSE® CRYSMEB 7 -CH3 4
Methyl-β-CD 7 -CH3 1.6
RAMEβ 7 -CH3 12.6
SBE7-β-CD 7 -(CH2)4-SO3Na 7
TRIMETHYL-β-CD 7 -CH3 21
HPγCD 8 -CH2-CHOH-CH3 4.8
RAMEγ 8 -CH3 14.4

α-CD, α-cyclodextrin; β-CD, β-cyclodextrin; CD, cyclodextrin; CRYSMEB, crystalline methylated-β-cyclodextrin; γ-CD, γ-cyclodextrin; HPαCD, 2-hydroxypropyl-α-cyclodextrin; HPβCD, 2-hydroxypropyl-β-cyclodextrin; HPγCD, 2-hydroxypropyl-γ-cyclodextrin; Methyl-β-CD, methyl-β-cyclodextrin ; RAMEα, randomly-methylated-α-cyclodextrin; RAMEβ, randomly-methylated-β-cyclodextrin; RAMEγ, randomly-methylated-γ-cyclodextrin; SBE7-β-CD, sulfobutylether-7-β-cyclodextrin; TRIMETHYL-β-CD, TRIMETHYL-β-cyclodextrin.