- Propamocarb
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- $1000.00
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2026-08-19
- CAS:24579-73-5
- Min. Order: 1kg
- Purity: 99%
- Supply Ability: 5000
- Propamocarb
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- $17430.00
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2026-07-01
- CAS:24579-73-5
- Min. Order: 1Tons
- Purity: 99.99
- Supply Ability: 200Tons
- Propamocarb
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-
2024-12-24
- CAS:24579-73-5
- Min. Order: 1g
- Purity: 99.99%
- Supply Ability: 20 tons
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| | Propamocarb Basic information |
| | Propamocarb Chemical Properties |
| Boiling point | bp18mm 139-141° | | density | 0.957±0.06 g/cm3(Predicted) | | refractive index | n20D 1.4490 | | Fp | >100 °C | | storage temp. | APPROX 4°C | | solubility | Chloroform (Slightly), Methanol (Slightly) | | pka | 12.73±0.46(Predicted) | | color | Colourless | | Merck | 13,7890 | | BRN | 2080745 | | Henry's Law Constant | 2.1×103 mol/(m3Pa) at 25℃, Keshavarz et al. (2022) | | Stability: | Stable. Incompatible with strong oxidizing agents. | | Major Application | agriculture
environmental | | InChI | 1S/C9H20N2O2/c1-4-8-13-9(12)10-6-5-7-11(2)3/h4-8H2,1-3H3,(H,10,12) | | InChIKey | WZZLDXDUQPOXNW-UHFFFAOYSA-N | | SMILES | CCCOC(=O)NCCCN(C)C | | LogP | 1.120 | | CAS DataBase Reference | 24579-73-5(CAS DataBase Reference) | | NIST Chemistry Reference | Propamocarb(24579-73-5) | | EPA Substance Registry System | Propamocarb (24579-73-5) |
| Hazard Codes | Xn | | Risk Statements | 22 | | WGK Germany | 2 | | RTECS | EZ8857000 | | HS Code | 29241990 | | Storage Class | 10 - Combustible liquids | | Hazard Classifications | Acute Tox. 4 Oral | | Hazardous Substances Data | 24579-73-5(Hazardous Substances Data) |
| | Propamocarb Usage And Synthesis |
| Chemical Properties | Propamocarb is colourless liquid | | Uses | Carbamate fungicide used in the agriculture industry | | Definition | Propamocarb is a carbamate ester that is the propyl ester of 3-(dimethylamino)propylcarbamic acid. It is a systemic fungicide, used (normally as the hydrochloride salt) for the control of soil, root and leaf diseases caused by oomycetes, particularly Phytophthora /ital> and Pythium species. | | Production Methods | Propamocarb is commercially synthesised by a process involves a nucleophilic substitution reaction where the amine group of DMAPA attacks the electrophilic carbon of the chloroformate, yielding propamocarb. The resulting compound is normally formulated as a hydrochloride salt (propamocarb-HCl) to enhance water solubility and stability | | Mechanism of action | Systemic, with protective action absorbed by roots and leaves and translocated. Lipid synthesis inhibitor. | | Pesticide Type | Fungicide |
| | Propamocarb Preparation Products And Raw materials |
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