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Mono-6-O-(p-toluenesulfonyl)-beta-cyclodextrin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 67217-55-4 Structure
  • Basic information

    1. Product Name: Mono-6-O-(p-toluenesulfonyl)-beta-cyclodextrin
    2. Synonyms: Mono-6-O-(p-toluenesulfonyl)-beta-cyclodextrin;Mono-6-O-Tosyl-beta-Cyclodextrin;β-Cyclodextrin, 6A-(4-methylbenzenesulfonate);mono-(6-p-toluenesulfonyl)-β-cyclodextrin;6A-(4-methylbenzenesulfonate)- -Cyclodextrin;Mono-6-O-(p-toluenesulfonyl)-&beta
    3. CAS NO:67217-55-4
    4. Molecular Formula: C49H76O37S
    5. Molecular Weight: 1289.17
    6. EINECS: 1312995-182-4
    7. Product Categories: N/A
    8. Mol File: 67217-55-4.mol
  • Chemical Properties

    1. Melting Point: 179 °C
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: White/Solid powder or crystals
    5. Density: 1.591g/cm3
    6. Refractive Index: 1.592
    7. Storage Temp.: 0-10°C
    8. Solubility: Soluble in DMF, DMSO. Insoluble in water, methanol, chloroform.
    9. PKA: 12.47±0.70(Predicted)
    10. CAS DataBase Reference: Mono-6-O-(p-toluenesulfonyl)-beta-cyclodextrin(CAS DataBase Reference)
    11. NIST Chemistry Reference: Mono-6-O-(p-toluenesulfonyl)-beta-cyclodextrin(67217-55-4)
    12. EPA Substance Registry System: Mono-6-O-(p-toluenesulfonyl)-beta-cyclodextrin(67217-55-4)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 67217-55-4(Hazardous Substances Data)

67217-55-4 Usage

Uses

Mono(6-O-p-tolylsulfonyl)-β-cyclodextrin (CAS# 67217-55-4) is carbohydrate used in the preparation of electroactive polyaniline/silica hybrid sol-gels. Recently, mono(6-O-p-tolylsulfonyl)-β-cyclodextrin has been proposed for use as a catalyst for atmospheric CO2 fixation by conversion to cuclic carbonate.

Check Digit Verification of cas no

The CAS Registry Mumber 67217-55-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,2,1 and 7 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 67217-55:
(7*6)+(6*7)+(5*2)+(4*1)+(3*7)+(2*5)+(1*5)=134
134 % 10 = 4
So 67217-55-4 is a valid CAS Registry Number.
InChI:InChI=1/C49H76O37S/c1-13-2-4-14(5-3-13)87(70,71)72-12-21-42-28(62)35(69)49(79-21)85-41-20(11-55)77-47(33(67)26(41)60)83-39-18(9-53)75-45(31(65)24(39)58)81-37-16(7-51)73-43(29(63)22(37)56)80-36-15(6-50)74-44(30(64)23(36)57)82-38-17(8-52)76-46(32(66)25(38)59)84-40-19(10-54)78-48(86-42)34(68)27(40)61/h2-5,15-69H,6-12H2,1H3/t15-,16-,17-,18-,19-,20-,21-,22-,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-/m1/s1

67217-55-4 Well-known Company Product Price

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  • TCI America

  • (M1381)  Mono-6-O-(p-toluenesulfonyl)-β-cyclodextrin  >85.0%(HPLC)

  • 67217-55-4

  • 200mg

  • 2,690.00CNY

  • Detail

67217-55-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Mono-6-O-(p-toluenesulfonyl)-beta-cyclodextrin

1.2 Other means of identification

Product number -
Other names ethane,ethyl 4-methylbenzenesulfonate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:67217-55-4 SDS

67217-55-4Synthetic route

p-toluenesulfonyl chloride
98-59-9

p-toluenesulfonyl chloride

β‐cyclodextrin
7585-39-9

β‐cyclodextrin

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

Conditions
ConditionsYield
With pyridine at 0 - 20℃;88%
With pyridine at 0 - 20℃;88%
With pyridine at 0 - 20℃;88%
p-toluenesulfonylanhydride
4124-41-8

p-toluenesulfonylanhydride

β‐cyclodextrin
7585-39-9

β‐cyclodextrin

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

Conditions
ConditionsYield
With sodium hydroxide In water at 20℃; for 0.166667h; Inert atmosphere;80%
With sodium hydroxide In water at 20℃; for 0.166667h;42%
With sodium hydroxide In water regioselective reaction;26%
p-toluenesulfonylanhydride
4124-41-8

p-toluenesulfonylanhydride

beta-cyclodextrin hydrate

beta-cyclodextrin hydrate

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

Conditions
ConditionsYield
With sodium hydroxide In water for 2h; Ambient temperature;61%
p-toluenesulfonyl chloride
98-59-9

p-toluenesulfonyl chloride

β-cyclodextrin

β-cyclodextrin

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

Conditions
ConditionsYield
With sodium hydroxide; copper(II) sulfate In acetonitrile for 4.5h; Substitution;48%
With sodium hydroxide at 0℃; for 3h;22%
With pyridine
N-tosylimidazole
2232-08-8

N-tosylimidazole

β‐cyclodextrin
7585-39-9

β‐cyclodextrin

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

Conditions
ConditionsYield
Stage #1: N-tosylimidazole; β‐cyclodextrin In water at 60℃; for 2h;
Stage #2: With sodium hydroxide In water at 20℃; for 0.666667h;
45.39%
Stage #1: N-tosylimidazole; β‐cyclodextrin In water for 2h;
Stage #2: With sodium hydroxide In water for 0.666667h;
45.39%
In water at 23℃; for 4h;43%
p-toluenesulfonyl chloride
98-59-9

p-toluenesulfonyl chloride

beta-cyclodextrin hydrate

beta-cyclodextrin hydrate

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

Conditions
ConditionsYield
With sodium hydroxide In water at 0 - 5℃; for 5h;28%
β-cyclodextrine

β-cyclodextrine

p-toluenesulfonyl chloride
98-59-9

p-toluenesulfonyl chloride

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

Conditions
ConditionsYield
With pyridine
toluene-4-sulfonic acid
104-15-4

toluene-4-sulfonic acid

β‐cyclodextrin
7585-39-9

β‐cyclodextrin

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

Conditions
ConditionsYield
With sodium hydroxide In water at -7 - 0℃; for 2h;4.2 g
With sodium hydroxide In water; acetonitrile at 10℃; for 4h;
β‐cyclodextrin
7585-39-9

β‐cyclodextrin

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

Conditions
ConditionsYield
In water
β‐cyclodextrin
7585-39-9

β‐cyclodextrin

tosyl derivative

tosyl derivative

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

Conditions
ConditionsYield
With ammonium chloride; sodium hydroxide at 20℃; for 2h;
mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

mono(6-azido-6-deoxy)β-cyclodextrin
98169-85-8

mono(6-azido-6-deoxy)β-cyclodextrin

Conditions
ConditionsYield
With sodium azide; potassium iodide In N,N-dimethyl-formamide100%
With sodium azide In dimethyl sulfoxide at 90℃; for 12h;100%
With sodium azide100%
mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

C42H68O35

C42H68O35

Conditions
ConditionsYield
With trimethylamine-N-oxide; dimethyl sulfoxide at 70℃; for 16h;100%
mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

Propargylamine
2450-71-7

Propargylamine

mono‐6‐deoxy‐6‐propynylamino‐β‐cyclodextrin
947740-17-2

mono‐6‐deoxy‐6‐propynylamino‐β‐cyclodextrin

Conditions
ConditionsYield
at 55℃; for 28h; Inert atmosphere;100%
at 80℃; for 96h; Inert atmosphere;99.1%
In N,N-dimethyl-formamide at 20℃; for 48h; Schlenk technique; Inert atmosphere;97%
at 75℃; for 20h;88.6%
at 65℃; for 24h; Inert atmosphere;83.2%
1-methyl-1H-imidazole
616-47-7

1-methyl-1H-imidazole

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

mono-6-deoxy-6-(3-methylidmiazolium)-β-cyclodextrin tosylate

mono-6-deoxy-6-(3-methylidmiazolium)-β-cyclodextrin tosylate

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 90℃; for 48h;99%
mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

N,N,N'-trimethyl-1,3-propanediamine
4543-96-8

N,N,N'-trimethyl-1,3-propanediamine

6I-((3-(dimethylamino)-1-(methyl)propyl)amino)-6I-deoxy-β-cyclodextrin
1638613-43-0

6I-((3-(dimethylamino)-1-(methyl)propyl)amino)-6I-deoxy-β-cyclodextrin

Conditions
ConditionsYield
In neat (no solvent) at 70℃; Inert atmosphere;99%
mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

ethylenediamine
107-15-3

ethylenediamine

mono-6-deoxy-6-(2-aminoethylamino)-β-cyclodextrin
60984-63-6

mono-6-deoxy-6-(2-aminoethylamino)-β-cyclodextrin

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 65℃; for 3h; Inert atmosphere;98.4%
at 70℃; for 14h;97%
at 70℃; for 3h; Product distribution / selectivity; Neat (no solvent);95%
propylamine
107-10-8

propylamine

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

C45H77NO34*C7H8O3S

C45H77NO34*C7H8O3S

Conditions
ConditionsYield
In N,N-dimethyl-formamide for 5h; Heating;98%
N-octylimidazole
21252-69-7

N-octylimidazole

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

C53H89N2O34(1+)*C7H7O3S(1-)

C53H89N2O34(1+)*C7H7O3S(1-)

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 90℃; for 48h;98%
Benzoyl bromide
618-32-6

Benzoyl bromide

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

C189H156O57S

C189H156O57S

Conditions
ConditionsYield
With pyridine at 0 - 20℃; for 18h; Inert atmosphere;98%
mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

Trimethylenediamine
109-76-2

Trimethylenediamine

6-[(2-aminopropyl)amino]-6-deoxy-β-cyclodextrin
131991-59-8

6-[(2-aminopropyl)amino]-6-deoxy-β-cyclodextrin

Conditions
ConditionsYield
at 70℃; for 24h;97.9%
In N,N-dimethyl-formamide at 39.9℃; for 24h;93%
at 70℃; for 10h;71%
1-Butylimidazole
4316-42-1

1-Butylimidazole

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

C49H81N2O34(1+)*C7H7O3S(1-)

C49H81N2O34(1+)*C7H7O3S(1-)

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 90℃; for 48h;97%
mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

N-butylamine
109-73-9

N-butylamine

C46H79NO34*C7H8O3S

C46H79NO34*C7H8O3S

Conditions
ConditionsYield
In N,N-dimethyl-formamide for 5h; Heating;97%
mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

1-pentanamine
110-58-7

1-pentanamine

C47H81NO34*C7H8O3S

C47H81NO34*C7H8O3S

Conditions
ConditionsYield
In N,N-dimethyl-formamide for 5h; Heating;96%
mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

ethanolamine
141-43-5

ethanolamine

6-deoxy-6-hydroxylethylamino-β-cyclodextrin
162615-68-1

6-deoxy-6-hydroxylethylamino-β-cyclodextrin

Conditions
ConditionsYield
at 85℃; for 0.5h; Microwave irradiation;95%
In N,N-dimethyl-formamide at 80℃; for 1h; Irradiation;90%
at 110℃; for 20h;88%
2,2',2''-triaminotriethylamine
4097-89-6

2,2',2''-triaminotriethylamine

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

6-deoxy-6{2-[bis(2-aminoethyl)amino]ethylamino}-β-cyclodextrin

6-deoxy-6{2-[bis(2-aminoethyl)amino]ethylamino}-β-cyclodextrin

Conditions
ConditionsYield
at 85℃; for 0.5h; Microwave irradiation;95%
With 1-methyl-pyrrolidin-2-one; potassium iodide at 70℃; for 4h;57%
mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

mono-[6-deoxy-6-(6-sulfanyl-9H-purine)]-β-cyclodextrin

mono-[6-deoxy-6-(6-sulfanyl-9H-purine)]-β-cyclodextrin

Conditions
ConditionsYield
With triethylamine In N,N-dimethyl-formamide at 60℃; for 72h;95%
mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

2,2'-iminobis[ethanol]
111-42-2

2,2'-iminobis[ethanol]

6-deoxy-6-dihydroxyethylamino-β-cyclodextrin

6-deoxy-6-dihydroxyethylamino-β-cyclodextrin

Conditions
ConditionsYield
at 85℃; for 0.5h; Microwave irradiation;95%
for 12h; Heating;42.68%
at 70℃; for 12h;
morpholine
110-91-8

morpholine

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

6-deoxy-6-N-morpholine-β-cyclodextrin
82679-33-2

6-deoxy-6-N-morpholine-β-cyclodextrin

Conditions
ConditionsYield
at 85℃; for 0.5h; Microwave irradiation;95%
N',N'-diisopropyl-ethane-1,2-diamine
121-05-1

N',N'-diisopropyl-ethane-1,2-diamine

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

6-deoxy-6-N,N'-diisopropyl-aminoethylamino-bcyclodextrin
1393337-75-1

6-deoxy-6-N,N'-diisopropyl-aminoethylamino-bcyclodextrin

Conditions
ConditionsYield
at 85℃; for 0.5h; Microwave irradiation;95%
mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

N,N-dimethylethylenediamine
108-00-9

N,N-dimethylethylenediamine

6-deoxy-6-N,N'-dimethyl-aminoethylamino-β-cyclodextrin

6-deoxy-6-N,N'-dimethyl-aminoethylamino-β-cyclodextrin

Conditions
ConditionsYield
at 85℃; for 0.5h; Microwave irradiation;95%
mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

6-deoxy-6-mercapto-β-cyclodextrin
81644-55-5

6-deoxy-6-mercapto-β-cyclodextrin

Conditions
ConditionsYield
Stage #1: mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin With thiourea In N,N-dimethyl-formamide at 75℃; for 48h;
Stage #2: With sodium metabisulfite; sodium hydroxide In water at 20℃; for 0.5h;
Stage #3: With hydrogenchloride; Trichloroethylene In water at 20℃; for 0.166667h; pH=3; Sonication;
94%
Stage #1: mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin With sodium hydroxide; thiourea In water at 80℃; for 9h;
Stage #2: With hydrogenchloride In water at 20℃; pH=4;
67%
With thiourea In N,N-dimethyl-formamide at 75℃; for 48h;64.29%
2-perfluorohexylethanethiol
34451-26-8

2-perfluorohexylethanethiol

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

6A-deoxy,6A-(3-perfluorohexylpropanethio)-cyclomaltoheptose

6A-deoxy,6A-(3-perfluorohexylpropanethio)-cyclomaltoheptose

Conditions
ConditionsYield
Stage #1: mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin With sodium methylate In methanol at 20℃; for 2h;
Stage #2: 2-perfluorohexylethanethiol In N,N-dimethyl-formamide at 70℃; for 24h;
94%
mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

1-allylimidazole
31410-01-2

1-allylimidazole

mono-6A-deoxy-6-(1-allylimidazolium)-β-cyclodextrin tosylate

mono-6A-deoxy-6-(1-allylimidazolium)-β-cyclodextrin tosylate

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 85℃; for 12h; Inert atmosphere;94%
In N,N-dimethyl-formamide at 85℃;
mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

ethylenediamine
107-15-3

ethylenediamine

C86H144N2O68

C86H144N2O68

Conditions
ConditionsYield
With Dowex resin In 1-methyl-pyrrolidin-2-one for 24h;93%
In N,N-dimethyl-formamide at 75℃; for 8h;0.97 g
In N,N-dimethyl-formamide at 20℃; for 12h;
mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

N,N',N'-trimethylenediamine
142-25-6

N,N',N'-trimethylenediamine

6I-((2-(dimethylamino)-1-(methyl)ethyl)amino)-6I-deoxy-β-cyclodextrin
157429-57-7

6I-((2-(dimethylamino)-1-(methyl)ethyl)amino)-6I-deoxy-β-cyclodextrin

Conditions
ConditionsYield
In neat (no solvent) at 70℃; Inert atmosphere;93%
mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

1-amino-2-propene
107-11-9

1-amino-2-propene

mono-6-(allylammmonium)-6-deoxy-β-cyclodextrin tosylate

mono-6-(allylammmonium)-6-deoxy-β-cyclodextrin tosylate

Conditions
ConditionsYield
In N,N-dimethyl-formamide for 5h; Heating;92%
3-Methylpyridine
108-99-6

3-Methylpyridine

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

mono[6-(m-picolinyl)-6-deoxy]-β-cyclodextrin

mono[6-(m-picolinyl)-6-deoxy]-β-cyclodextrin

Conditions
ConditionsYield
for 12h; Heating;91%
picoline
108-89-4

picoline

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

mono-6-deoxy-6-(4-methylpyridinium)-β-cyclodextrin-p-toluenesulfonate
1033766-93-6

mono-6-deoxy-6-(4-methylpyridinium)-β-cyclodextrin-p-toluenesulfonate

Conditions
ConditionsYield
at 85℃; for 12h;91%
mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

2-(2-Aminoethylamino)ethanol
111-41-1

2-(2-Aminoethylamino)ethanol

C46H80N2O35

C46H80N2O35

Conditions
ConditionsYield
at 75℃; for 72h;90.5%
at 75℃; for 72h;90.5%
mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin
67217-55-4

mono-6-deoxy-6-(p-tolylsulphonyl)-β-cyclodextrin

2-methoxyethylamine
109-85-3

2-methoxyethylamine

6-Deoxy-6-(2-methoxyethylamino)-β-cyclodextrin
98366-79-1

6-Deoxy-6-(2-methoxyethylamino)-β-cyclodextrin

Conditions
ConditionsYield
at 75℃; for 72h;90.2%
In N,N-dimethyl-formamide at 50℃;30%

67217-55-4Relevant articles and documents

Influence of degree of substitution on the host-guest inclusion complex between ionic liquid substituted β-cyclodextrins with 2,4-dichlorophenol: An electrochemical, NMR and molecular docking studies

Rasdi, Fairuz Liyana Mohd,Rahim, Nurul Yani,Hasim, Fara Wahida,Prabu, Samikannu,Jumbri, Khairulazhar,Manan, Ninie Suhana Abdul,Mohamad, Sharifah

, (2019)

A mono- and di-substituted ionic liquid-β-cyclodextrin (β-CD-ILs) were synthesized and their host-guest inclusion complex with 2, 4-dichlorophenol (2,4-DCP) were evaluated by electrochemical study. First, both β-CD-ILs which is β-CD-1-BIMOTs and β-CD-2-BIMOTs were fabricated on carbon paste electrode (CPE) for determination of 2,4-DCP. The cyclic voltammetry results indicate that both β-CD-IL/CPEs exhibit higher oxidation peak current compared to native β-CD/CPE. Both complexes possess high sensitivity, stability and reproducibility. However, as the degree of substitution of ionic liquid (IL) increases, the selectivity of β-CD-IL towards 2,4-DCP decreases. Thus, it can be deduced that the degree of substitution of IL is influencing the host-guest inclusion complex of β-CD-ILs with 2,4-DCP.

Characterization and enhanced antioxidant activity of the cysteinyl β-cyclodextrin-baicalein inclusion complex

Kim, Hwanhee,Yiluo, Hu,Park, Seyeon,Lee, Jae Yung,Cho, Eunae,Jung, Seunho

, (2016)

Baicalein is a type of flavonoid isolated from the roots of a medicinal plant, Scutellaria baicalensis. Although it has attracted considerable attention due to its antiviral, anti-tumor, and anti-inflammatory activities, its limited aqueous solubility inhibits the clinical application of this flavonoid. The present study aimed to prepare and characterize a host-guest complex in an effort to improve the solubility and antioxidant activity of baicalein. The host molecule is a macrocyclic β-cyclodextrin (β-CD) functionalized with cysteine for a synergetic effect. The structure of the synthesized cysteinyl β-CD was analyzed using nuclear magnetic resonance (NMR) spectroscopy and mass spectrometry. The inclusion complex with baicalein was studied by UV-vis, NMR spectroscopy, scanning electron microscopy, and X-ray powder diffractometry. The formed cysteinyl β-CD/baicalein inclusion complex efficiently improved the solubility and antioxidant ability of baicalein. Therefore, we suggest that the present cysteinyl β-CD is a potential host molecule for inclusion complexation and for bioavailability augmentation.

Preparation of 2D molecularly imprinted materials based on mesoporous silicas via click reaction

Xu, Zhifeng,Deng, Peihong,Tang, Siping,Kuang, Daizhi,Zhang, Fuxing,Li, Junhua

, p. 8418 - 8426 (2014)

The two-dimensional (2D) molecular imprinting approach has attracted extensive research interest in recent years due to its potential advantages such as simple construction, fast template removal and rapid mass transfer. In this study, a new 2D imprinting

Pseudopolyanions based on poly(NIPAAM-co-β-cyclodextrin methacrylate) and ionic liquids

Amajjahe, Sadik,Choi, Soowhan,Munteanu, Maricica,Ritter, Helmut

, p. 3435 - 3437 (2008)

(Chemical Equation Presented) A fine host: Copolymers from methacrylated β-cyclodextrin and N-isopropylacrylamide form inclusion complexes with anions of ionic liquids (IL; see picture). Complex formation alters the solubility properties of the copolymer,

Biotinylated cyclooligosaccharides for paclitaxel solubilization

Cho, Eunae,Jung, Seunho

, (2018)

The poor water solubility of paclitaxel causes significant problems in producing cancer therapeutic formulations. Here, we aimed to solubilize paclitaxel using biocompatible cyclic carbohydrates. Generally recognized as safe, labeled β-cyclodextrin (β-CD), a cyclic α-1,4-glucan consisting of seven glucoses, was prepared, and bio-sourced cyclosophoraoses (CyS), which are unbranched cyclic β-1,2-glucans with 17–23 glucose units, were purified using various chromatographic methods from Rhizobium leguminosarum cultural broth. For effective targeting, CyS and β-CD were modified with a biotinyl moiety in a reaction of mono-6-amino CyS and mono-6-amino-β-CD with N-hydroxysuccinimide ester of biotinamidohexanoic acid. Interestingly, the aqueous solubility of paclitaxel was enhanced 10.3- and 3.7-fold in the presence of biotinyl CyS and biotinyl β-CD, respectively. These findings suggest that biotin-appended cyclooligosaccharides can be applied to improve the delivery of paclitaxel.

Fabrication of new generation of co-delivery systems based on graphene-g-cyclodextrin/chitosan nanofiber

Adeli, Mohsen,Rashidipour, Marzieh,Sattari, Shabnam,Soleimani, Khadijeh,Tehrani, Abbas Dadkhah

, p. 1126 - 1134 (2020)

Although many techniques have been devoted to promote therapeutic purposes of drug carrier systems, however, there are still many challenges in this area. Here, we designed co-loaded delivery systems, composed of curcumin loaded cyclodextrin-graphene oxid

Supramolecular poly(N-acryloylmorpholine)-b-poly(D,L-lactide) pseudo-block copolymer via host-guest interaction for drug delivery

Ramesh, Kalyan,Anugrah, Daru Seto Bagus,Lim, Kwon Taek

, p. 12 - 21 (2018)

In the present study, a pseudo-block copolymer was prepared from β-cyclodextrin terminated poly(N-acryloylmorpholine) (β-CD-PNAM) and adamantine-terminated linear poly(D,L-lactide) (AD-PDLLA), through host-guest interaction between β-CD and AD groups. Ini

Rational design for cooperative recognition of specific nucleobases using β-cyclodextrin-modified DNAs and fluorescent ligands on DNA and RNA scaffolds

Futamura, Akika,Uemura, Asuka,Imoto, Takeshi,Kitamura, Yusuke,Matsuura, Hirotaka,Wang, Chun-Xia,Ichihashi, Toshiki,Sato, Yusuke,Teramae, Norio,Nishizawa, Seiichi,Ihara, Toshihiro

, p. 10526 - 10535 (2013)

We propose a binary fluorimetric method for DNA and RNA analysis by the combined use of two probes rationally designed to work cooperatively. One probe is an oligonucleotide (ODN) conjugate bearing a β-cyclodextrin (β-CyD). The other probe is a small repo

Efficient synthesis of pure monotosylated beta-cyclodextrin and its dimers

Tripodo, Giuseppe,Wischke, Christian,Neffe, Axel T.,Lendlein, Andreas

, p. 59 - 63 (2013)

6-O-Monotosyl-β-cyclodextrin (mono-Ts-βCD) is one of the most important intermediates in the production of substituted βCD. So far, performing the monotosylation reaction and, in particular, the purification steps was challenging, relied on toxic solvents

Preparation and Stability Evaluation of Size-Controllable PDHCA-β-CD Nanoparticles as Drug Carrier

Chu, Hong,Zhao, Xue,Liu, Shirong,Ni, Zhongbin,Shi, Dongjian,Chen, Mingqing

, p. 1125 - 1132 (2017)

A novel biocompatible polymer was prepared by grafting the derivate of β-cyclodextrin (6-SH-β-CD) onto poly(3,4-dihydroxycinnamic acid) (PDHCA) via Michael addition. PDHCA-β-CD nanoparticles were prepared by the self-assembly of amphiphilic PDHCA-β-CD pol

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