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inquiryReliable quality 29390-67-8 low price 6-Monodeoxy-6-monoamino-beta-cyclodextrine global trader Cyclodextrin (CD) it is a cyclic oligosaccharide obtained by the degradation of starch under the action of cyclodextrin glycosyltransferase, which is form
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inquiryProduct name: Mono-(6-Amino-6-Deoxy)-Beta-Cyclodextrin CAS No.:29390-67-8 Molecule Formula:C42H71NO34 Molecule Weight:1134.00 Purity: 98% Package: 25kg/drum Description:White powder Manufacture Standards:Enterprise Standard TESTI
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inquiryCAS29390-67-8 6-Monodeoxy-6-monoamino-beta-cyclodextrine Application:CAS29390-67-8 6-Monodeoxy-6-monoamino-beta-cyclodextrine
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inquirymono(6-azido-6-deoxy)β-cyclodextrin
6(I)-amino-6(I)-deoxycyclomaltoheptaose
Conditions | Yield |
---|---|
With triphenylphosphine In N,N-dimethyl-formamide for 1h; Ambient temperature; | 99% |
Stage #1: mono(6-azido-6-deoxy)β-cyclodextrin With triphenylphosphine In N,N-dimethyl-formamide for 2h; Stage #2: With water In N,N-dimethyl-formamide for 0.5h; Heating; | 97% |
Stage #1: mono(6-azido-6-deoxy)β-cyclodextrin With triphenylphosphine In N,N-dimethyl-formamide at 20℃; Stage #2: With ammonium hydroxide In N,N-dimethyl-formamide at 20℃; for 0.166667h; | 95% |
mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
6(I)-amino-6(I)-deoxycyclomaltoheptaose
Conditions | Yield |
---|---|
With ammonia In water at 20℃; for 168h; | 90% |
With ammonium hydroxide In water at 50℃; for 72h; | 79% |
With ammonium hydroxide In water at 85℃; for 0.5h; Microwave irradiation; | 60% |
6(I)-amino-6(I)-deoxycyclomaltoheptaose
Conditions | Yield |
---|---|
With ammonium hydroxide In water at 20℃; | 88% |
mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
A
6(I)-amino-6(I)-deoxycyclomaltoheptaose
B
β‐cyclodextrin
Conditions | Yield |
---|---|
With ammonia In water at 60℃; for 5h; Product distribution / selectivity; | A 70% B 30% |
mono(6-azido-6-deoxy)β-cyclodextrin
A
6(I)-amino-6(I)-deoxycyclomaltoheptaose
B
β‐cyclodextrin
Conditions | Yield |
---|---|
With ammonium hydroxide; triphenylphosphine 1) DMF; Yield given. Multistep reaction. Yields of byproduct given; |
6-deoxy-6-(N-hydroxylamino)-β-cyclodextrin
6(I)-amino-6(I)-deoxycyclomaltoheptaose
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In water under 1292.9 Torr; for 20h; |
Conditions | Yield |
---|---|
With water In various solvent(s) at 25℃; pH=4.0; Kinetics; Further Variations:; Reagents; |
A
6(I)-amino-6(I)-deoxycyclomaltoheptaose
Conditions | Yield |
---|---|
In water-d2 at 25℃; Equilibrium constant; |
β‐cyclodextrin
6(I)-amino-6(I)-deoxycyclomaltoheptaose
Conditions | Yield |
---|---|
Stage #1: β‐cyclodextrin With p-toluenesulfonyl chloride In pyridine Stage #2: With sodium azide In N,N-dimethyl-formamide Stage #3: With palladium on activated charcoal; hydrazine hydrate |
1,1,2,2-tetrachloroethane
6(I)-amino-6(I)-deoxycyclomaltoheptaose
Conditions | Yield |
---|---|
With sodium azide; triphenylphosphine In [(2)H6]acetone; water |
6(I)-amino-6(I)-deoxycyclomaltoheptaose
Conditions | Yield |
---|---|
With ammonium hydroxide |
6(I)-amino-6(I)-deoxycyclomaltoheptaose
N-acetyl-DL-tryptophan
Conditions | Yield |
---|---|
With benzotriazol-1-ol; dicyclohexyl-carbodiimide In N,N-dimethyl-formamide for 48h; Ambient temperature; | 91% |
6(I)-amino-6(I)-deoxycyclomaltoheptaose
bromoacetic acid
mono-6-deoxy-6-bromoacetylamino-β-cyclodextrin
Conditions | Yield |
---|---|
Stage #1: bromoacetic acid With benzotriazol-1-ol; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide for 3h; Stage #2: 6(I)-amino-6(I)-deoxycyclomaltoheptaose In N,N-dimethyl-formamide for 2h; Further stages.; | 91% |
N-Fmoc L-Phe
6(I)-amino-6(I)-deoxycyclomaltoheptaose
Conditions | Yield |
---|---|
With benzotriazol-1-ol; dicyclohexyl-carbodiimide In N,N-dimethyl-formamide at 0℃; for 15h; | 90% |
succinic acid anhydride
6(I)-amino-6(I)-deoxycyclomaltoheptaose
mono-6'-deoxy-6'-amidosuccinyl-β-cyclomaltoheptaose
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 20℃; for 12h; | 90% |
Stage #1: succinic acid anhydride; 6(I)-amino-6(I)-deoxycyclomaltoheptaose With triethylamine In N,N-dimethyl-formamide at 50℃; for 12h; Stage #2: With water In N,N-dimethyl-formamide at 20℃; for 1h; Stage #3: With sodium methylate In methanol at 20℃; for 1h; | 71.2% |
In N,N-dimethyl-formamide at 20℃; for 18h; | 55% |
6(I)-amino-6(I)-deoxycyclomaltoheptaose
1H-pyrazole-1-carboximidamide hydrochloride
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; for 24h; | 89% |
With N-ethyl-N,N-diisopropylamine In water at 20℃; for 24h; | 87% |
With N-ethyl-N,N-diisopropylamine In water at 20℃; for 48h; | 85% |
With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; for 72h; |
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