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CAS No.: | 70193-21-4 |
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Name: | TRICHLAMIDE |
Article Data: | 7 |
Molecular Structure: | |
Formula: | C13H16 Cl3 N O3 |
Molecular Weight: | 340.634 |
Synonyms: | Hataclean;N-(1-Butoxy-2,2,2-trichloroethyl)-2-hydroxybenzamide;N-(1-Butoxy-2,2,2-trichloroethyl)salicylamide; NK 483; Trichlamide; WL 105305 |
Density: | 1.353 g/cm3 |
Melting Point: | 71~73℃71.0~73.0℃ |
Boiling Point: | 457.4 °C at 760 mmHg |
Flash Point: | 230.4 °C |
Safety: | Moderately toxic by intraperitoneal route. Low toxicity by ingestion and skin contact. Experimental reproductive effects. When heated to decomposition it emits toxic vapors of NOx and Cl−. |
PSA: | 58.56000 |
LogP: | 4.02590 |
IUPAC Name: N-(1-butoxy-2,2,2-trichloroethyl)-2-hydroxybenzamide
Synonyms of N-(l-butoxy-2,2,2-trichloroethyl) salicylamide (CAS NO.70193-21-4): Trichlamide [ISO] ; (RS)-N-(1-Butoxy-2,2,2-trichloroethyl)salicylamide ; BRN 2882884 ; Hataclean ; N-(1-Butoxy-2,2,2-trichloroethyl)-2-hydroxybenzamide ; NK 483 ; Trichlamide ; WL 105305 ; Benzamide, N-(1-butoxy-2,2,2-trichloroethyl)-2-hydroxy- ;
CAS NO: 70193-21-4
Molecular Formula of N-(l-butoxy-2,2,2-trichloroethyl) salicylamide (CAS NO.70193-21-4): C13H16Cl3NO3
Molecular Weight: 340.63
H bond acceptors: 4
H bond donors: 2
Freely Rotating Bonds: 7
Polar Surface Area: 38.77 Å2
Index of Refraction: 1.557
Molar Refractivity: 81.13 cm3
Molar Volume: 251.6 cm3
Surface Tension: 47.8 dyne/cm
Density: 1.353 g/cm3
Flash Point: 230.4 °C
Enthalpy of Vaporization: 74.5 kJ/mol
Boiling Point: 457.4 °C at 760 mmHg
Vapour Pressure: 5.52E-09 mmHg at 25°C
Molecular Structure:
N-(l-butoxy-2,2,2-trichloroethyl) salicylamide (CAS NO.70193-21-4) can make pesticides.
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
mouse | LD50 | intraperitoneal | 1590mg/kg (1590mg/kg) | Japan Pesticide Information. Vol. (56), Pg. 12, 1990. | |
mouse | LD50 | oral | > 5gm/kg (5000mg/kg) | Nippon Noyaku Gakkaishi. Journal of the Pesticide Science Society of Japan. Vol. 13, Pg. 395, 1988. | |
mouse | LD50 | skin | > 5gm/kg (5000mg/kg) | Nippon Noyaku Gakkaishi. Journal of the Pesticide Science Society of Japan. Vol. 13, Pg. 395, 1988. | |
mouse | LD50 | subcutaneous | > 5gm/kg (5000mg/kg) | Nippon Noyaku Gakkaishi. Journal of the Pesticide Science Society of Japan. Vol. 13, Pg. 395, 1988. | |
rat | LD50 | intraperitoneal | 1140mg/kg (1140mg/kg) | Nippon Noyaku Gakkaishi. Journal of the Pesticide Science Society of Japan. Vol. 13, Pg. 395, 1988. | |
rat | LD50 | oral | 7590mg/kg (7590mg/kg) | Nippon Noyaku Gakkaishi. Journal of the Pesticide Science Society of Japan. Vol. 13, Pg. 395, 1988. | |
rat | LD50 | skin | > 5gm/kg (5000mg/kg) | Nippon Noyaku Gakkaishi. Journal of the Pesticide Science Society of Japan. Vol. 13, Pg. 395, 1988. | |
rat | LD50 | subcutaneous | > 5gm/kg (5000mg/kg) | Japan Pesticide Information. Vol. (56), Pg. 12, 1990. |
Moderately toxic by intraperitoneal route. Low toxicity by ingestion and skin contact. Experimental reproductive effects. When heated to decomposition it emits toxic vapors of NOx and Cl−.