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33978

Supelco

2-Acetamido-5-nitrothiazole

VETRANAL®, analytical standard

Synonym(s):

N-(5-Nitro-2-thiazolyl)acetamide

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About This Item

Empirical Formula (Hill Notation):
C5H5N3O3S
CAS Number:
140-40-9
Molecular Weight:
187.18
EC Number:
205-414-7
MDL number:
MFCD00022438
UNSPSC Code:
41116107
PubChem Substance ID:
329754718

grade

analytical standard

product line

VETRANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

forensics and toxicology
pharmaceutical (small molecule)

format

neat

SMILES string

CC(=O)Nc1ncc(s1)[N+]([O-])=O

InChI

1S/C5H5N3O3S/c1-3(9)7-5-6-2-4(12-5)8(10)11/h2H,1H3,(H,6,7,9)

InChI key

UJRRDDHEMZLWFI-UHFFFAOYSA-N

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

VETRANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302

Precautionary Statements

P264 - P270 - P301 + P312 - P501

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

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O A Beliaeva
Klinichna khirurhiia, (7)(7), 32-33 (1999-02-16)
The experience of treatment of 18 patients with intraabdominal abscess using the regional laparostomy conduction and introducing nitazol, immobilized on polymethylsiloxane, in the abscess cavity, was summarized.
J P Raynaud et al.
American journal of veterinary research, 42(1), 51-53 (1981-01-01)
A swine dysentery (SD) model that produces consistent, homogeneous, and severe SD was used in 2 experiments to compare the prophylactic effectiveness of 5 commercially available swine feed additive products. Under the conditions of these studies, carbadox and carbadox +
[The immunomodulating therapy of odontogenic phlegmons with complexes of antibacterial preparations and water-soluble polymers for medical use].
V N Tsarev et al.
Stomatologiia, Spec No, 88-88 (1996-01-01)
John J O'Shea et al.
Nature reviews. Rheumatology, 9(3), 173-182 (2013-02-20)
The molecular biology revolution coupled with the development of monoclonal antibody technology enabled remarkable progress in rheumatology therapy, comprising an array of highly effective biologic agents. With advances in understanding of the molecular nature of immune cell receptors came elucidation
N F Kalinichenko
Mikrobiolohichnyi zhurnal (Kiev, Ukraine : 1993), 60(1), 83-91 (1998-06-11)
The antibacterial activity of protistocide drug nitazole has been revealed for the first time in the 80's at the Laboratory of Clinical Microbiology of the Mechnikov Research Institute of Microbiology and Immunology. Unlike other imidazoles, such as metronidazole and tinidazole
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