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About This Item
Empirical Formula (Hill Notation):
C3H3NS
CAS Number:
Molecular Weight:
85.13
FEMA Number:
3615
Beilstein:
103852
EC Number:
Council of Europe no.:
11642
MDL number:
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
15.028
NACRES:
NA.21
Recommended Products
biological source
synthetic
Quality Level
grade
Halal
Kosher
Agency
meets purity specifications of JECFA
Assay
≥99%
refractive index
n20/D 1.538 (lit.)
bp
117-118 °C (lit.)
density
1.2 g/mL at 25 °C (lit.)
application(s)
flavors and fragrances
Documentation
see Safety & Documentation for available documents
food allergen
no known allergens
Organoleptic
nutty
SMILES string
c1cscn1
InChI
1S/C3H3NS/c1-2-5-3-4-1/h1-3H
InChI key
FZWLAAWBMGSTSO-UHFFFAOYSA-N
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Disclaimer
For R&D or non-EU Food use. Not for retail sale.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Flam. Liq. 2
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
71.6 °F - closed cup
Flash Point(C)
22 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Yukiko Kiniwa et al.
PloS one, 10(5), e0124094-e0124094 (2015-05-21)
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Mohammad Sayed Alam et al.
Chemical & pharmaceutical bulletin, 62(12), 1259-1268 (2014-12-03)
A novel series of 2-arylidenehydrazinyl-4-arylthiazole analogues (3a-p) was designed and synthesized in excellent yields using a rapid, simple, efficient methodology. Sixteen novel compounds were screened for in vitro antimicrobial activities against eleven bacteria, namely, Staphylococcus aureus, Listeria monocytogenes, Enterococcus faecalis
Eita Sasaki et al.
Nature, 510(7505), 427-431 (2014-05-13)
Sulphur is an essential element for life and is ubiquitous in living systems. Yet how the sulphur atom is incorporated into many sulphur-containing secondary metabolites is poorly understood. For bond formation between carbon and sulphur in primary metabolites, the major
Maria Hayashi et al.
Journal of nutritional science and vitaminology, 61(3), 270-274 (2015-08-01)
The biosynthetic pathways of the thiazole moiety of thiamin were studied in the archaeon Halobacterium salinarum. Thiamin is generated by the union of 4-amino-5-hydroxymethyl-2-methylpyrimidine (pyrimidine) and 5-(2-hydroxyethyl)-4-methylthiazole (thiazole). The biosynthesis of thiazole is different in facultative anaerobes, aerobes and eukaryotes.
Lisa Nezvitsky et al.
American journal of physiology. Renal physiology, 307(5), F634-F647 (2014-07-25)
The unfolded protein response and endoplasmic reticulum-associated degradation (ERAD) contribute to injury in renal glomerular diseases, including those mediated by complement C5b-9. In the present study, we address the role of protein-tyrosine phosphatase 1B (PTP1B) in complement-mediated glomerular injury and
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