Name | 2-ethyl-3-methyl-pentanamide Axiquel Nirvanil |
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Synonyms |
2-ethyl-3-methylpentanamide
Valnoctamide |
Description | Valnoctamide (Valmethamide), a derivative of valproate, suppresses benzodiazepine-refractory status epilepticus. Valnoctamide (Valmethamide) acts directly on GABAA receptors[1]. |
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Related Catalog | |
Target |
GABAA receptor[1] |
References |
Density | 0.883g/cm3 |
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Boiling Point | 274.4ºC at 760mmHg |
Melting Point | 113.5-114ºC |
Molecular Formula | C8H17NO |
Molecular Weight | 143.22700 |
Flash Point | 119.8ºC |
Exact Mass | 143.13100 |
PSA | 43.09000 |
LogP | 2.24430 |
Index of Refraction | 1.438 |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
|
Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H302 |
RIDADR | NONH for all modes of transport |
RTECS | YV5950000 |
HS Code | 2924199090 |
~% 4171-13-5 |
Literature: Kaufmann, Dan; Bialer, Meir; Shimshoni, Jakob Avi; Devor, Marshall; Yagen, Boris Journal of Medicinal Chemistry, 2009 , vol. 52, # 22 p. 7236 - 7248 |
~% 4171-13-5 |
Literature: Freifelder,M. et al. Journal of Organic Chemistry, 1961 , vol. 26, p. 203 - 206 |
~% 4171-13-5 |
Literature: Kaufmann, Dan; Yagen, Boris; Minert, Anne; Wlodarczyk, Bogdan; Finnell, Richard H.; Schurig, Volker; Devor, Marshall; Bialer, Meir Neuropharmacology, 2010 , vol. 58, # 8 p. 1228 - 1236 |
~% 4171-13-5 |
Literature: Katznelson; Kondakowa Doklady Akademii Nauk SSSR, 1934 , p. II 24 Chem. Zentralbl., 1935 , vol. 106, # I p. 2521 |
~% 4171-13-5 |
Literature: Katznelson; Kondakowa Doklady Akademii Nauk SSSR, 1934 , p. II 24 Chem. Zentralbl., 1935 , vol. 106, # I p. 2521 |
Precursor 5 | |
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DownStream 0 |
HS Code | 2924199090 |
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Summary | 2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |