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W361518

Sigma-Aldrich

Thiazole

≥99%

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Synonym(s):
1,3-thiazole
Empirical Formula (Hill Notation):
C3H3NS
CAS Number:
Molecular Weight:
85.13
FEMA Number:
3615
Beilstein/REAXYS Number:
103852
EC Number:
Council of Europe no.:
11642
MDL number:
PubChem Substance ID:
Flavis number:
15.028
NACRES:
NA.21

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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1 of 4

This Item
W326704W334006W371602
Thiazole ≥99%

W361518

Thiazole

2,4-Dimethyl-5-acetylthiazole ≥97%

W326704

2,4-Dimethyl-5-acetylthiazole

2-Ethoxythiazole ≥99%, FG

W334006

2-Ethoxythiazole

4-Methylthiazole ≥98%, FG

W371602

4-Methylthiazole

organoleptic

nutty

organoleptic

musty; nutty; earthy

organoleptic

musty; vegetable; nutty

organoleptic

green; vegetable; nutty

biological source

synthetic

biological source

synthetic

biological source

synthetic

biological source

synthetic

food allergen

no known allergens

food allergen

no known allergens

food allergen

no known allergens

food allergen

no known allergens

assay

≥99%

assay

≥97%

assay

≥99%

assay

≥98%

agency

meets purity specifications of JECFA

agency

meets purity specifications of JECFA

agency

meets purity specifications of JECFA

agency

meets purity specifications of JECFA

Disclaimer

For R&D or non-EU Food use. Not for retail sale.

pictograms

FlameExclamation mark

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

71.6 °F - closed cup

flash_point_c

22 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Yukiko Kiniwa et al.
PloS one, 10(5), e0124094-e0124094 (2015-05-21)
Immunotherapy has emerged as a promising strategy for the treatment of metastatic melanoma. Clinical studies have demonstrated the feasibility of cancer immunotherapy using tumor antigens recognized by CD8(+) T cells. However, the overall immune responses induced by these antigens are
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
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
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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