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About This Item
Linear Formula:
CH3CH2CH2CH2SNa
CAS Number:
Molecular Weight:
112.17
PubChem Substance ID:
UNSPSC Code:
12352100
Beilstein/REAXYS Number:
3594199
MDL number:
Assay:
≥95.0% (RT)
Form:
powder
SMILES string
CCCCS[Na]
InChI
1S/C4H10S.Na/c1-2-3-4-5;/h5H,2-4H2,1H3;/q;+1/p-1
InChI key
VTLWRSNWWLIJTQ-UHFFFAOYSA-M
grade
technical
assay
≥95.0% (RT)
form
powder
Quality Level
Other Notes
Salts of alkanethiols are versatile intermediates for the synthesis of various thiol esters and thioethers. In contrast to the stenchy gaseous or liquid thiols, the salts are easy to handle solids.; Alkanethiolates are strong nucleophiles and thus efficient reagents for SN2 type dealkylations of hindered esters and lactones; Cleavage of aryl methyl ethers
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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P.A. Bartlett et al.
Tetrahedron Letters, 4459-4459 (1970)
G.I. Feutrill et al.
Tetrahedron Letters, 1327-1327 (1970)
L. Testaferri et al.
Synthesis, 751-751 (1983)
W.R. Vaughan et al.
The Journal of Organic Chemistry, 27, 739-739 (1962)
Grigor B Bantchev et al.
Journal of agricultural and food chemistry, 57(4), 1282-1290 (2009-01-27)
Butanethiol was used in ultraviolet-initiated thiol-ene reaction with canola and corn oils to produce sulfide-modified vegetable oils (SMVO). The crude SMVO product was successfully purified by solvent extraction, vacuum evaporation, and silica gel chromatography. The SMVO products were characterized by
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