CHEMICAL AND PHYSICAL PROPERTIES
| Boiling Point | BP: 139-141 °C at 18 mm Hg |
|---|---|
| Melting Point | Colorless, odorless crystals. MP: 44-45 °C. Solulbility at 25 °C (g/100 mL): water >70; dichloromethane >43; methanol >50. VP at 25 °C: 5X10-6 torr /Propamocarb hydrochloride/ |
| Flash Point | >100 °C (>212 °F) |
| Solubility | In water, 9.0X10+5 mg/L at 20 °C, pH 7.0 |
| Vapor Pressure | 5.48X10-2 mm Hg at 25 °C |
| LogP | log Kow = 1.12 |
| Henry's Law Constant | Henry's Law constant = 1.48X10-9 atm-cu m/mol at 25 °C (1.5X10-4 Pa-cu m/mol) |
| Stability/Shelf Life | Stable under recommended storage conditions. |
| Ionization Efficiency | Positive |
| Refractive Index | Index of refraction: 1.4490 at 20 °C/D |
| Dissociation Constants | 9.48 |
| Collision Cross Section | 144.69 Ų [M+H]+ |
| Kovats Retention Index | 1361.5 |
| Other Experimental Properties | Very soluble in water, ethanol, dichloroethane; sparingly soluble in toluene, hexane |
SAFETY INFORMATION
| Signal word | Warning |
|---|---|
| Pictogram(s) |
![]() Exclamation Mark Irritant GHS07 |
| GHS Hazard Statements |
H302:Acute toxicity,oral |
COMPUTED DESCRIPTORS
| Molecular Weight | 188.27 g/mol |
|---|---|
| XLogP3 | 1.2 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 7 |
| Exact Mass | 188.152477885 g/mol |
| Monoisotopic Mass | 188.152477885 g/mol |
| Topological Polar Surface Area | 41.6 Ų |
| Heavy Atom Count | 13 |
| Formal Charge | 0 |
| Complexity | 138 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently-Bonded Unit Count | 1 |
| Compound Is Canonicalized | Yes |
PRODUCT INTRODUCTION
description
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 and Pythium species. It has a role as a xenobiotic, an environmental contaminant and an antifungal agrochemical. It is a carbamate ester, a tertiary amino compound and a carbamate fungicide. It is functionally related to a propan-1-ol.

