Propamocarb structure
|
Common Name | Propamocarb | ||
|---|---|---|---|---|
| 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 |
|---|---|
| Synonym | More Synonyms |
| Description | Propamocarb is a systemic fungicide. Propamocarb is widely used to protect cucumbers, tomatoes and other plants from pathogens[1]. |
|---|---|
| Related Catalog | |
| References |
| Density | 1.0±0.1 g/cm3 |
|---|---|
| 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 |
| InChIKey | WZZLDXDUQPOXNW-UHFFFAOYSA-N |
| SMILES | CCCOC(=O)NCCCN(C)C |
| Storage condition | APPROX 4°C |
| Stability | Stable. Incompatible with strong oxidizing agents. |
CHEMICAL IDENTIFICATION
|
| Symbol |
GHS07 |
|---|---|
| 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 |
|---|---|
| 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 ... |
|
|
Microbial degradation of the carbamate pesticides desmedipham, phenmedipham, promecarb, and propamocarb.
Bull. Environ. Contam. Toxicol. 27(4) , 529-33, (1981)
|
|
|
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 |