Mercapto-β-cyclodextrin

Mercapto-β-cyclodextrin Suppliers list
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Products Intro: Product Name:mono(6-mercapto-6-deoxy)-beta-cyclodextrin
CAS:81644-55-5
Purity:98% Package:1KG;1USD
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Products Intro: Product Name:Mono-(6-Mercapto-6-deoxy)-β-Cyclodextrin
CAS:81644-55-5
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Products Intro: Product Name:Mono-(6-Mercapto-6-deoxy)-β-cyclodextrin
CAS:81644-55-5
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Products Intro: Product Name:Mercapto-β-cyclodextrin
CAS:81644-55-5
Purity:99.0% Min Package:1g;1.1USD Remarks:ISO 9001:2015 REACH Approved Manufacturer
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Products Intro: Product Name:Mono-(6-Mercapto-6-deoxy)-beta-Cyclodextrin
CAS:81644-55-5
Purity:98%min Package:1g;USD

Mercapto-β-cyclodextrin manufacturers

Mercapto-β-cyclodextrin Basic information
Product Name:Mercapto-β-cyclodextrin
Synonyms:Mercapto-β-cyclodextrin;Mercapto-beta-cyclodextrin;Mono-(6-Mercapto-6-deoxy)-beta--Cyclodextrin;6-Mercapto-6-deoxy-β-Cyclodextrin;Mono-(6-Mercapto-6-deoxy)-β-cyclodextrin;Mercapto-β-cyclodextrin ISO 9001:2015 REACH;6-Deoxy-6-mercapto-β-cyclodextrin;β-Cyclodextrin, 6A-thio-
CAS:81644-55-5
MF:C42H70O34S
MW:1151.05
EINECS:1312995-182-4
Product Categories:
Mol File:81644-55-5.mol
Mercapto-β-cyclodextrin Structure
Mercapto-β-cyclodextrin Chemical Properties
Boiling point 1534.4±60.0 °C(Predicted)
density 1.609±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka9.42±0.10(Predicted)
InChIKeyKBQFCFNGXZCYMC-JXMPPWEANA-N
Safety Information
MSDS Information
Mercapto-β-cyclodextrin Usage And Synthesis
Synthesis
Mono-6-O-(p-toluenesulfonyl)-beta-cyclodextrin

67217-55-4

Mercapto-β-cyclodextrin

81644-55-5

The general procedure for the synthesis of 6-mercapto-6-deoxy-β-cyclodextrin from mono-6-O-(p-toluenesulfonyl)-β-cyclodextrin is as follows: to a 50 mL round-bottomed flask equipped with a magnetic stirring bar and Schlenk fittings were added 1.00 g (0.776 mmol) of mono-6-O-(p-toluenesulfonyl)-β-cyclodextrin, 0.59 g (7.75 mmol) thiourea (purchased from Aldrich) and 7.8 mL of 0.1 N NaOH solution. The resulting mixture was heated and stirred at 80 °C for 6 h under nitrogen protection. Subsequently, 0.62 g (15.5 mmol) of sodium hydroxide was added and the reaction continued to be heated at 80 °C and under nitrogen atmosphere for 1 hour. After the reaction mixture was cooled to room temperature, the pH was adjusted to 4.0 with 10% HCl solution. the total volume of the reaction solution was adjusted to 20 mL, which was subsequently cooled in an ice bath, and 0.8 mL of tetrachloroethylene was added. The reaction mixture was stirred vigorously at 0 °C for 0.5 h. The precipitated solid was collected through a fine glass feed funnel. The resulting solid was vacuum dried overnight to yield 0.60 g (67% yield) of white amorphous solid product.

References[1] Chemistry - A European Journal, 2014, vol. 20, # 35, p. 10944 - 10952
[2] Patent: EP1133318, 2007, B1. Location in patent: Page/Page column 32-33
[3] Chinese Journal of Chemistry, 2017, vol. 35, # 7, p. 1125 - 1132
[4] Chemical Communications, 2011, vol. 47, # 45, p. 12388 - 12390
[5] Angewandte Chemie - International Edition, 2012, vol. 51, # 2, p. 450 - 454
Mercapto-β-cyclodextrin Preparation Products And Raw materials
Raw materialsMono-6-O-(p-toluenesulfonyl)-beta-cyclodextrin-->Sodium hydroxide-->Thiourea-->Hydrochloric acid
Tag:Mercapto-β-cyclodextrin(81644-55-5) Related Product Information
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