| Identification | Back Directory | [Name]
TRICHLAMIDE | [CAS]
70193-21-4 | [Synonyms]
nk483
hataclean
TRICHLAMIDE
Salicylfungi amide
TRICHLAMIDE STANDARD
trichlamide (bsi, draft e-iso, draft f-iso)
N-(1-Butoxy-2,2,2-trichloroethyl)salicylamide
n-(l-butoxy-2,2,2-trichloroethyl)salicylamide
(rs)-n-(1-butoxy-2,2,2-trichloroethyl)salicylamide
n-(1-butoxy-2,2,2-trichloroethyl)-2-hydroxy-benzamid
n-(1-butoxy-2,2,2-trichloroethyl)-2-hydroxybenzamide
BenzaMide,N-(1-butoxy-2,2,2-trichloroethyl)-2-hydroxy- | [EINECS(EC#)]
215-958-7 | [Molecular Formula]
C13H16Cl3NO3 | [MDL Number]
MFCD00128927 | [MOL File]
70193-21-4.mol | [Molecular Weight]
340.63 |
| Chemical Properties | Back Directory | [Melting point ]
71～73℃71.0～73.0℃ | [Boiling point ]
169.5°C (rough estimate) | [density ]
1.4549 (rough estimate) | [refractive index ]
1.6200 (estimate) | [storage temp. ]
0-6°C |
| Hazard Information | Back Directory | [Uses]
Trichlamide is a fungicide used in crops and on produce. Pesticide. | [Definition]
ChEBI:Trichlamide is a member of salicylamides and a benzamide fungicide. | [Production Methods]
Trichlamide is commercially synthesised through a process that begins with the preparation of salicylamide, which is reacted with 1-butoxy-2,2,2-trichloroethyl chloride under basic conditions, typically using a non-aqueous solvent like dichloromethane and a base such as triethylamine. This nucleophilic substitution yields trichlamide, a compound characterised by its trichlorinated aliphatic side chain and phenolic benzamide core. The reaction is conducted under controlled temperature to ensure selectivity and minimise side reactions. | [Mechanism of action]
Inhibition of microsomal lipid peroxidation, non-systemic | [Pesticide Type]
Fungicide |
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