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About This Item
Empirical Formula (Hill Notation):
C4H4N2O2S
CAS Number:
Molecular Weight:
144.15
EC Number:
207-985-8
UNSPSC Code:
12352200
PubChem Substance ID:
Beilstein/REAXYS Number:
120663
MDL number:
grade
purum
assay
≥98.0% (S)
drug control
regulated under CDSA - not available from Sigma-Aldrich Canada
ign. residue
≤0.1%
mp
245 °C (dec.) (lit.)
SMILES string
O=C1CC(=O)NC(=S)N1
InChI
1S/C4H4N2O2S/c7-2-1-3(8)6-4(9)5-2/h1H2,(H2,5,6,7,8,9)
InChI key
RVBUGGBMJDPOST-UHFFFAOYSA-N
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Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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The synthesis of melanins, which are the most common animal pigments, is influenced by glutathione (GSH), a key intracellular antioxidant. At high GSH levels, pheomelanin (the lightest melanin form) is produced, whereas production of eumelanin (the darkest melanin form) does
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Journal of agricultural and food chemistry, 60(38), 9589-9594 (2012-09-07)
The ability of the spectrophotometric thiobarbituric acid reactive substances (TBARS) test to determine malondialdehyde (MDA) in various food matrices was evaluated. MDA was extracted from the foods; the extract reacted with thiobarbituric acid (TBA); and the formed TBA-MDA adduct was
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