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2-(Butylamino)ethanethiol

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2-(Butylamino)ethanethiol Basic information
Product Name:2-(Butylamino)ethanethiol
Synonyms:2-n-Butylaminoethanethiol;2-(butylamino)-ethanethio;Ethanethiol, 2-(butylamino)-;(butylamino)ethanethiol;N-Butylcysteamine;2-(Butylamino)ethanetiol;2-N-butylaminoethylthiol;2-(Butylamino)ethanethiol
CAS:5842-00-2
MF:C6H15NS
MW:133.26
EINECS:227-431-9
Product Categories:Organic Building Blocks;Sulfur Compounds;Thiols/Mercaptans;Building Blocks;Chemical Synthesis;Organic Building Blocks;Sulfur Compounds
Mol File:5842-00-2.mol
2-(Butylamino)ethanethiol Structure
2-(Butylamino)ethanethiol Chemical Properties
Boiling point 112-115 °C10 mm Hg(lit.)
density 0.901 g/mL at 25 °C(lit.)
refractive index n20/D 1.4711(lit.)
Fp 163 °F
pka8.91±0.10(Predicted)
form liquid
InChI1S/C6H15NS/c1-2-3-4-7-5-6-8/h7-8H,2-6H2,1H3
InChIKeyOUMFAUYLXGTBCX-UHFFFAOYSA-N
SMILESCCCCNCCS
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36/37/39
RIDADR UN 3334
WGK Germany 3
RTECS KJ0339000
Storage Class10 - Combustible liquids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
Skin Sens. 1
STOT SE 3
MSDS Information
ProviderLanguage
SigmaAldrich English
2-(Butylamino)ethanethiol Usage And Synthesis
Uses
  • Photocatalytic oxidation of VX simulant 2-(butylamino)ethanethiol.: This paper investigates the photocatalytic oxidation of 2-(Butylamino)ethanethiol, a simulant for the nerve agent VX. The findings indicate that photocatalytic processes can effectively degrade sulfur-containing compounds, suggesting applications in decontamination and hazardous material management. This research provides insights into the environmental remediation of toxic chemical agents (Vorontsov et al., 2004).
2-(Butylamino)ethanethiol Preparation Products And Raw materials
Tag:2-(Butylamino)ethanethiol(5842-00-2) Related Product Information
CHES Sodium taurocholate Taurodeoxycholic acid sodium salt Ethanethiol Taurocholic acid 2-(Butylamino)ethanethiol Taurochenodeoxycholic acid sodium salt Taurolithocholic acid sodium salt 3alpha-Hydroxy-5beta-cholan-24-oic acid N-[2-sulfoethyl]amide 3-sulfate disodium salt Sodium taurodehydrocholate 2-Propylthiazolidine S-Methylglutathione Phenythilone Thiazolidine, 2-butyl- AKOS BBS-00005153 GLUTATHIONE REDUCED, IMMOBILIZED ON AGAROSE CL-4B 2-n-Decylaminoethanethiol BILIRUBIN CONJUGATE, DITAURATE, DISODIUM SALT