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CAS RN: 55981-09-4 | Product Number: N1031
Nitazoxanide
Purity: >98.0%(T)(HPLC)
Synonyms:
- 2-(Acetyloxy)-N-(5-nitro-2-thiazolyl)benzamide
- NTZ
Product Documents:
Size | Unit Price | Same Day | 2-3 Business Days |
---|---|---|---|
200MG |
$29.00
|
Contact Us | 4 |
1G |
$95.00
|
2 | Contact Us |
5G |
$317.00
|
30 | Contact Us |
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to order our products. The above prices do not include freight cost, customs, and other charges to the destination.
* The storage conditions are subject to change without notice.
Supplemental Product Information:
This product is a sample for RUO (research use only). Do not use this product for any purpose other than testing and research.
Product Number | N1031 |
Purity / Analysis Method | >98.0%(T)(HPLC) |
Molecular Formula / Molecular Weight | C__1__2H__9N__3O__5S = 307.28 |
Physical State (20 deg.C) | Solid |
Storage Temperature | Refrigerated (0-10°C) |
Condition to Avoid | Heat Sensitive |
Packaging and Container | 1G-Glass Bottle with Plastic Insert (View image), 200MG-Glass Bottle with Plastic Insert (View image) |
CAS RN | 55981-09-4 |
Reaxys Registry Number | 1225475 |
PubChem Substance ID | 354333058 |
Merck Index (14) | 6567 |
MDL Number | MFCD00416599 |
Specifications
Appearance | White to Orange to Green powder to crystal |
Purity(HPLC) | min. 98.0 area% |
Purity(Neutralization titration) | min. 98.0 % |
Melting point | 198.0 to 202.0 °C |
Properties (reference)
Melting Point | 200 °C |
Maximum Absorption Wavelength | 416(Phosphate buffer sol.) nm |
GHS
Pictogram | |
Signal Word | Warning |
Hazard Statements | H302 : Harmful if swallowed. H315 : Causes skin irritation. H319 : Causes serious eye irritation. |
Precautionary Statements | P501 : Dispose of contents/ container to an approved waste disposal plant. P270 : Do not eat, drink or smoke when using this product. P264 : Wash skin thoroughly after handling. P280 : Wear protective gloves/ eye protection/ face protection. P302 + P352 : IF ON SKIN: Wash with plenty of water. P337 + P313 : If eye irritation persists: Get medical advice/ attention. P305 + P351 + P338 : IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. P362 + P364 : Take off contaminated clothing and wash it before reuse. P332 + P313 : If skin irritation occurs: Get medical advice/ attention. P301 + P312 + P330 : IF SWALLOWED: Call a POISON CENTER/doctor if you feel unwell. Rinse mouth. |
Related Laws:
RTECS# | VN7830000 |
Transport Information:
H.S.code* | 2934.10-000 |
Application
Nitazoxanide: A Thiazolide Antiprotozoal and Antiviral Agent
Nitazoxanide is originally developed as a thiazolide antiprotozoal agent that shows excellent in vitro activity against a variety of microorganisms, including a broad range of protozoa and helminths. Nitazoxanide is a prodrug, and following oral administration in animals, nitazoxanide is rapidly hydrolyzed to an active metabolite, tizoxanide [T3862] (desacetyl-nitazoxanide) by esterase. The antiprotozoal activity of tizoxanide is believed to be due to interference with the pyruvate:ferredoxin oxidoreductase (PFOR) enzyme-dependent electron transfer reaction which is essential to anaerobic energy metabolism. Recently, antiviral activity of nitazoxanide against a broad range of other RNA and DNA viruses such as hepatitis B virus, hepatitis C virus and influenza virus has been recognized in in vitro systems. Nitazoxanide is synergistic with neuraminidase inhibitors, and also inhibits the replication of a broad range of viruses. (The product is for research purpose only.)
References
- In vitro evaluation of activities of nitazoxanide and tizoxanide against anaerobes and aerobic organisms
- Efficacy of nitazoxanide against Cryptosporidium parvum in cell culture and in animal models
- Nitazoxanide: a new thiazolide antiparasitic agent (a review)
- Nitazoxanide a review of its use in the treatment of gastrointestinal infections
- Nitazoxanide, tizoxanide and other thiazolides are potent inhibitors of hepatitis B virus and hepatitis C virus replication
- Nitazoxanide: A first-in-class broad-spectrum antiviral agent (a review)
PubMed Literature
Articles/Brochures
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