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CAS RN: 70374-39-9 | Product Number: L0239
Lornoxicam
Purity: >98.0%(HPLC)(N)
- 6-Chloro-4-hydroxy-2-methyl-N-(2-pyridyl)-2H-thieno[2,3-e][1,2]thiazine-3-carboxamide 1,1-Dioxide
Size | Unit Price | Hyderabad | Japan* | Quantity |
---|---|---|---|---|
1G |
₹12,400.00
|
Contact Us | 34 |
|
5G |
₹18,500.00
|
2 | 10 |
|
*Upon orders receipt, Hyderabad stocks will be dispatched on the same day.
*Items available in Japan warehouse will be dispatched in 10-12 working days.
*INR price is exclusive of domestic taxes applicable.
*TCI frequently reviews storage conditions to optimize them. Please note that the latest information on the storage temperature for the products is described on our website.
Product Number | L0239 |
Purity / Analysis Method | >98.0%(HPLC)(N) |
Molecular Formula / Molecular Weight | C__1__3H__1__0ClN__3O__4S__2 = 371.81 |
Physical State (20 deg.C) | Solid |
Storage Temperature | Frozen (-20°C) |
Condition to Avoid | Heat Sensitive |
CAS RN | 70374-39-9 |
Reaxys Registry Number | 1039965 |
PubChem Substance ID | 125308046 |
Merck Index (14) | 5582 |
MDL Number | MFCD00866163 |
Appearance | White to Yellow powder to crystal |
Purity(HPLC) | min. 98.0 area% |
Purity(with Total Nitrogen) | min. 98.0 % |
Melting Point | 230 °C(dec.) |
Solubility (soluble in) | Dimethylformamide |
Pictogram | |
Signal Word | Danger |
Hazard Statements | H300 : Fatal if swallowed. |
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. P301 + P310 + P330 : IF SWALLOWED: Immediately call a POISON CENTER/doctor. Rinse mouth. P405 : Store locked up. |
RTECS# | XJ9095000 |
UN Number | UN2811 |
Class | 6.1 |
Packing Group | II |
References
- Effects of Lornoxicam, piroxicam, and Meloxicam in a model of thermal hind paw hyperalgesia induced by formalin injection in rat tail
- The analgesic NSAID lornoxicam inhibits cyclooxygenase (COX)-1/-2, inducible nitric oxide synthase (iNOS), and the formation of interleukin (IL)-6 in vitro
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