| Identification | More | [Name]
Propamocarb | [CAS]
24579-73-5 | [Synonyms]
PROPAMOCARB
PROPYL-3-(DIMETHYLAMINO)PROPYLCARBAMATE
(3-(dimethylamino)propyl)-carbamicacipropylester
nor-am39744
propamocarbe
sn39744
PROPAMOCARB PESTANAL (PROPYL 3-(DI METHY
Carbamic acid, 3-(dimethylamino)propyl-, propyl ester
propamocarb (ansi,bsi,iso)
NOR-AM
Tuco
N-[3-(Dimethylamino)propyl]carbamic acid propyl ester | [EINECS(EC#)]
247-125-9 | [Molecular Formula]
C9H20N2O2 | [MDL Number]
MFCD00078717 | [Molecular Weight]
188.27 | [MOL File]
24579-73-5.mol |
| Chemical Properties | Back Directory | [Appearance]
colourless liquid | [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) | [form ]
neat | [pka]
12.73±0.46(Predicted) | [color ]
Colourless | [Stability:]
Stable. Incompatible with strong oxidizing agents. | [Merck ]
13,7890 | [BRN ]
2080745 | [Henry's Law Constant]
2.1×103 mol/(m3Pa) at 25℃, Keshavarz et al. (2022) | [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]
24579-73-5(EPA Substance) |
| Hazard Information | Back Directory | [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 |
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| Company Name: |
J & K SCIENTIFIC LTD.
|
| Telephone: |
18210857532 18210857532 |
| Website: |
https://www.jkchemical.com |
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