Skip to Content
Merck
CN

33978

2-Acetamido-5-nitrothiazole

VETRANAL®, analytical standard

Synonym(s):

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

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

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

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

InChI key

UJRRDDHEMZLWFI-UHFFFAOYSA-N

InChI

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

SMILES string

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

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

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

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our Documents section.

If you need assistance, please contact Customer Support

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

S V Tarasenko et al.
Stomatologiia, 79(2), 17-19 (2000-05-17)
Combined drugs with a hydrophilic base, nitacide and hyposol-n, were used in combined therapy of acute purulent inflammations of the maxillofacial area. Time course of clinical parameters and changes in microflora were studied in patients administered different local treatments with
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
[Search for contact spermatocidal agents].
L N Kopteva
Akusherstvo i ginekologiia, (2)(2), 67-70 (1992-02-01)
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.
L A Blatun et al.
Antibiotiki i khimioterapiia = Antibiotics and chemoterapy [sic], 43(12), 20-24 (1999-03-18)
Nitazole, a drug from the nitrotiazole group, was shown to be active in vitro against bacteroides, peptococci, peptostreptococci, clostridia, staphylococci, colibacilli and streptococci. By its activity and antibacterial spectrum nitazole had some advantages over metronidazole, a drug from the nitroimidazole
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service