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CAS RN: 14222-60-7 | Product Number: P2302

Prothionamide


Purity: >98.0%(T)(HPLC)
Synonyms:
  • 2-Propylpyridine-4-carbothioamide
  • 2-Propylthioisonicotinamide
Product Documents:
5G
$47.00
4   2   ≥40 
25G
$152.00
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Product Number P2302
Purity / Analysis Method >98.0%(T)(HPLC)
Molecular Formula / Molecular Weight C__9H__1__2N__2S = 180.27 
Physical State (20 deg.C) Solid
Storage Temperature Room Temperature (Recommended in a cool and dark place, <15°C)
CAS RN 14222-60-7
Reaxys Registry Number 118164
PubChem Substance ID 253660961
Merck Index (14) 7891
MDL Number

MFCD00464119

Specifications
Appearance Light yellow to Yellow to Orange powder to crystal
Purity(HPLC) min. 98.0 area%
Purity(Nonaqueous Titration) min. 98.0 %
Melting point 141.0 to 145.0 °C
Properties (reference)
Melting Point 143 °C
Solubility in water Insoluble
Solubility (soluble in) Ethanol
GHS
Pictogram 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.
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.
P302 + P352 : IF ON SKIN: Wash with plenty of soap and water.
P332 + P313 : If skin irritation occurs: Get medical advice/ attention.
P362 : Take off contaminated clothing and wash before reuse.
P301 + P312 + P330 : IF SWALLOWED: Call a POISON CENTER/doctor if you feel unwell. Rinse mouth.
Related Laws:
RTECS# NS0650000
Transport Information:
HS Number 2933.39.9200
Application
Prothionamide: A Thioamide Anti-Tuberculosis Agent

Prothionamide and ethionamide [E0695] are thioamide anti-tuberculosis agents. They have activity against Mycobacterium tuberculosis, Mycobacterium leprae murium and Mycobacterium avium. The precise mechanisms of action remain unknown, but it has been reported that the thioamides are prodrugs that are oxidatively converted to their active forms by the flavin monooxygenase EtaA of Mycobacterium tuberculosis.

References


PubMed Literature


TCIMAIL
Product Documents (Note: Some products will not have analytical charts available.)
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