6-Tritylmercapto-hexanoic acid

6-Tritylmercapto-hexanoic acid Suppliers list
Company Name: ATK CHEMICAL COMPANY LIMITED
Tel: +undefined-21-51877795
Email: ivan@atkchemical.com
Products Intro: CAS:80441-55-0
Purity:98% Package:10MG;50MG;100MG,1G,5G,10G.100G
Company Name: GL Biochem (Shanghai) Ltd.
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Products Intro: Product Name:6-(Tritylthio)-hexanoic acid
CAS:80441-55-0
Purity:0.98 Package:50G,1Kg, 50Kg
Company Name: BOC Sciences
Tel: 16314854226; +16314854226
Email: inquiry@bocsci.com
Products Intro: Product Name:6-(Tritylthio)-hexanoic acid
CAS:80441-55-0
Purity:>= 98% (HPLC) Remarks:BOC Sciences also provides custom synthesis services for 6-(Tritylthio)-hexanoic acid.
Company Name: Jilin Chinese Academy of Sciences-yanshen Technology
Tel: +undefined18143011203
Email: info@chemextension.com
Products Intro: Product Name:6-(Tritylthio)hexanoic acid
CAS:80441-55-0
Purity:95%+ Package:1g;5g;10g;25g;50g;100g; Remarks:accept Custom Synthesis Services, support large packing
Company Name: J & K SCIENTIFIC LTD.  
Tel: 010-82848833 400-666-7788
Email: jkinfo@jkchemical.com
Products Intro: Product Name:6-(Tritylthio)hexanoic acid, 97%
CAS:80441-55-0
Purity:97% Package:1G
6-Tritylmercapto-hexanoic acid Basic information
Product Name:6-Tritylmercapto-hexanoic acid
Synonyms:6-Tritylsulfanyl-hexanoic acid;6-(Tritylthio)-hexanoic acid;6-Tritylmercapto-hexanoic acid;6-[(triphenylmethyl)sulfanyl]hexanoic acid;Hexanoic acid, 6-[(triphenylmethyl)thio]-;6-[(Triphenylmethyl)thio]hexanoic acid;Ethane,1-bromo-2-(6-methoxyethoxy)-
CAS:80441-55-0
MF:C25H26O2S
MW:390.54
EINECS:
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Mol File:80441-55-0.mol
6-Tritylmercapto-hexanoic acid Structure
6-Tritylmercapto-hexanoic acid Chemical Properties
Boiling point 536.7±38.0 °C(Predicted)
density 1.147±0.06 g/cm3(Predicted)
pka4.77±0.10(Predicted)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26
HS Code 29163990
MSDS Information
6-Tritylmercapto-hexanoic acid Usage And Synthesis
Description6-(Tritylthio)hexanoic acid is a linker with a Tst group and a terminal carboxylic acid. The Tst group can be deprotected under acidic conditions to obtain the free thiol which can be used for further conjugations. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond.
Chemical PropertiesWhite powder
6-Tritylmercapto-hexanoic acid Preparation Products And Raw materials
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