24579-73-5

Basic information

• Product Name: Propamocarb
• 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
• CAS NO: 24579-73-5
• Molecular Formula: C₉H₂₀N₂O₂
• Molecular Weight: 188.27
• EINECS: 247-125-9
• Product Categories: FUNGICIDE;Alpha sort;CarbamatesPesticides&Metabolites;Fungicides;N-PAlphabetic;P;Pesticides;PON - PT;Agro-Products;Amines;NULL
• Mol File: 24579-73-5.mol
• Article Data: 10

Chemical Properties

• Boiling Point: bp18mm 139-141°
• Flash Point: >100 °C
• Appearance: colourless liquid
• Density: 0.957 g/cm³
• Vapor Pressure: 0.015mmHg at 25°C
• Refractive Index: n20D 1.4490
• Storage Temp.: APPROX 4°C
• Solubility: Chloroform (Slightly), Methanol (Slightly)
• PKA: 12.73±0.46(Predicted)
• Stability: Stable. Incompatible with strong oxidizing agents.
• Merck: 13,7890
• BRN: 2080745
• CAS DataBase Reference: Propamocarb(CAS DataBase Reference)
• NIST Chemistry Reference: Propamocarb(24579-73-5)
• EPA Substance Registry System: Propamocarb(24579-73-5)

Safety Data

• Hazard Codes: Xn
• Statements: 22
• WGK Germany: 2
• RTECS: EZ8857000
• Hazardous Substances Data: 24579-73-5(Hazardous Substances Data)

Usage

Description

Propamocarb, a carbamate ester and the propyl ester of 3-(dimethylamino)propylcarbamic acid, is a systemic fungicide. It is characterized by its colorless liquid form and is primarily used in the agriculture industry for the control of various soil, root, and leaf diseases.

Uses

Used in Agriculture Industry:
Propamocarb is used as a carbamate fungicide for the control of soil, root, and leaf diseases caused by oomycetes, particularly targeting Phytophthora and Pythium species. Its application helps in protecting crops from these harmful pathogens, ensuring a healthy growth and yield.

InChI:InChI=1/C9H20N2O2/c1-9(2,3)13-8(12)10-6-7-11(4)5/h6-7H2,1-5H3,(H,10,12)

Upstream product

• 71-23-8 propan-1-ol 
• 201230-82-2 carbon monoxide 
• 109-55-7 1-amino-3-(dimethylamino)propane 

Downstream Products

• 25606-41-1 propamocarb hydrochloride 

Relevant articles and documents

IMPROVED PROCESS FOR THE PREPARATION OF CARBAMATES

A process for the preparation of N-(dialkylaminoalkyl)-carbamic acid esters, in particular (propyl N-[3-(dimethylamino)propyl] carbamate) comprising an oxidative carbonylation reaction of a compound of general structure (II) wherein each of R1 and R2, equal to or different from each other, are independently selected from an alkyl group having 1 to 10 carbon atoms, which is optionally substituted by at least one halogen atom, an aryl group or an aralkyl group; R3 is selected from an alkyl group having 1 to 36 carbon atoms, which is optionally substituted by at least one halogen atom, an aryl group or an aralkyl group; each of R', R and R4, equal to or different from each other, are independently selected from H, an alkyl group having 1 to 10 carbon atoms, which is optionally substituted by at least one halogen atom, an aryl group or an aralkyl group; and n is an integer in the range from 1 to 8, with a hydroxyl compound of general formula (III), R3-OH (III) and in the presence of a catalyst system.

Pyrazolyl benzyl ether derivatives containing a fluoromethoxyimino group and use thereof as pesticides

The invention relates to novel pyrazolyl benzyl ethers, to a plurality of processes for their preparation and to their use for controlling harmful organisms.

Iminoacetic acid amides and their use as pest control agents

PCT No. PCT/EP96/04345 Sec. 371 Date Apr. 15, 1998 Sec. 102(e) Date Apr. 15, 1998 PCT Filed Oct. 7, 1996 PCT Pub. No. WO97/14673 PCT Pub. Date Apr. 24, 1997Iminoacetamides of the formula (I) in which A represents a single bond or optionally substituted alkylene, Q represents oxygen or sulphur, R1 represents respectively optionally substituted cycloalkyl, cycloalkenyl, aryl or heterocyclyl, R2 represents respectively optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkenyl, aryl or heterocyclyl, R3 represents hydrogen or respectively optionally substituted alkyl, alkenyl, alkinyl or cycloalkyl, R4 represents respectively optionally substituted cycloalkyl, cycloalkenyl, aryl or heterocyclcyl a process for their preparation, pesticidal compositions containing them, and their use for controlling pests.