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Merck
CN

71334

Sodium 1-butanethiolate

technical, ≥95.0% (RT)

Synonym(s):

1-Butanethiol sodium salt

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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
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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

pictograms

Corrosion

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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