Propamocarb structure
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Common Name | Propamocarb | ||
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CAS Number | 24579-73-5 | Molecular Weight | 188.267 | |
Density | 1.0±0.1 g/cm3 | Boiling Point | 264.0±42.0 °C at 760 mmHg | |
Molecular Formula | C9H20N2O2 | Melting Point | 45-55ºC | |
MSDS | Chinese USA | Flash Point | 113.4±27.9 °C | |
Symbol |
GHS07 |
Signal Word | Warning |
Use of PropamocarbPropamocarb is a systemic fungicide. Propamocarb is widely used to protect cucumbers, tomatoes and other plants from pathogens[1]. |
Name | propamocarb |
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Synonym | More Synonyms |
Description | Propamocarb is a systemic fungicide. Propamocarb is widely used to protect cucumbers, tomatoes and other plants from pathogens[1]. |
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Related Catalog | |
References |
Density | 1.0±0.1 g/cm3 |
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Boiling Point | 264.0±42.0 °C at 760 mmHg |
Melting Point | 45-55ºC |
Molecular Formula | C9H20N2O2 |
Molecular Weight | 188.267 |
Flash Point | 113.4±27.9 °C |
Exact Mass | 188.152481 |
PSA | 41.57000 |
LogP | 1.80 |
Vapour Pressure | 0.0±1.2 mmHg at 25°C |
Index of Refraction | 1.456 |
Storage condition | APPROX 4°C |
Stability | Stable. Incompatible with strong oxidizing agents. |
CHEMICAL IDENTIFICATION
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Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H302 |
Personal Protective Equipment | Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter |
Hazard Codes | Xn:Harmful; |
Risk Phrases | R22 |
RIDADR | NONH for all modes of transport |
RTECS | EZ8857000 |
HS Code | 2924199014 |
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% |
The influence of fungicides on the growth of Trichoderma asperellum.
Meded. Rijksuniv. Gent. Fak. Landbouwkd. Toegep. Biol. Wet. 67(2) , 291-8, (2002) Numbers of strains of Trichoderma asperellum are known as biological control agents of certain root pathogens of tomato (Lycopersicon esculentum). The restricted use of fungicides is sometimes useful ... |
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Microbial degradation of the carbamate pesticides desmedipham, phenmedipham, promecarb, and propamocarb.
Bull. Environ. Contam. Toxicol. 27(4) , 529-33, (1981)
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Effect of pesticides on estrogen receptor transactivation in vitro: a comparison of stable transfected MVLN and transient transfected MCF-7 cells.
Mol. Cell. Endocrinol. 244(1-2) , 20-30, (2005) The estrogenic potential of four pesticides (endosulfan, prochloraz, tolchlofos-methyl and propamocarb) was compared in parallel with 17beta-estradiol (E2) by reporter constructs in transient transfec... |
Propamocarb free base |
Banol turf fungicide |
Plantacur |
Plantacur E |
Tuco |
Propyl hydrogen [3-(dimethylamino)propyl]carbonimidate |
Propamocarb |
MFCD00078717 |
NOR-AM |
Propyl [3-(dimethylamino)propyl]carbamate |
Propyl (3-(dimethylamino)propyl)carbamate |
Methanol, 1-[[3-(dimethylamino)propyl]imino]-1-propoxy-, (E)- |
propyl N-[3-(dimethylamino)propyl]carbamate |
Carbamic acid, N-[3-(dimethylamino)propyl]-, propyl ester |
propyl 3-(dimethylamino)propylcarbamate |