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Safety Information

W361518

Sigma-Aldrich

Thiazole

≥99%

Synonym(s):

1,3-thiazole

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About This Item

Empirical Formula (Hill Notation):
C3H3NS
CAS Number:
288-47-1
Molecular Weight:
85.13
FEMA Number:
3615
Beilstein:
103852
EC Number:
206-021-3
Council of Europe no.:
11642
MDL number:
MFCD00005315
UNSPSC Code:
12164502
PubChem Substance ID:
24901810
Flavis number:
15.028
NACRES:
NA.21

biological source

synthetic

Quality Level

400

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.

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Danger

Hazard Statements

H225,H302

Hazard Classifications

Acute Tox. 4 Oral - Flam. Liq. 2

WGK

WGK 3

Flash Point(F)

closed cup

Flash Point(C)

closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

危险化学品

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
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
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.
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
Zhiyang Jia
OncoTargets and therapy, 8, 1561-1565 (2015-07-08)
The objective of the present investigation was to investigate the role of integrin-linked kinase (ILK) in the gemcitabine-resistant lung cancer cell line A549 and explore the underlying mechanism. Gemcitabine-resistant A549 (A549/GemR) cell line was established by pulse-exposed to moderate concentration
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