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

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

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.

Substituted imide derivatives

The present invention relates to novel substituted imide derivatives of the general formula (I) in which R1 represents optionally substituted cycloalkyl, R2 represents optionally substituted alkyl or optionally substituted cycloalkyl, R3 represents alkyl, alkoxy, alkylthio, amino, alkylamino or dialkylamino and R4 represents cyano or nitro, and to processes for their preparation and to their use for controlling animal pests and as herbicides.

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.

2-and 2,5-substituted phenylketoenols

PCT No. PCT/EP97/03973 Sec. 371 Date Jan. 28, 1999 Sec. 102(e) Date Jan. 28, 1999 PCT Filed Jul. 23, 1997 PCT Pub. No. WO98/05638 PCT Pub. Date Feb. 12, 1998The invention relates to novel phenyl-substituted cyclic ketoenols of the formula (I) in which Het represents one of the groups in which A, B, D, G, X and Z are each as defined in the description, to a plurality of processes and intermediates for their preparation, and to their use as pesticides.

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.

Microbicidal benzotriazoles

Novel benzotriazoles of the formula STR1 in which R, X1, X2, X3, X4 and Y have the meanings given in the description, and their acid addition salts and metal salt complexes, a process for the preparation of these substances and their use as microbicides in crop protection and in material protection.

Halogen alkenyl azolyl microbicides

Novel halogenoalkenyl-azolyl derivatives of the formula STR1 in which R1 represents optionally substituted alkyl, optionally substituted alkenyl, optionally substituted cycloalkyl, optionally substituted aryl or represents optionally substituted heteroaryl, R2 represents alkyl, halogenoalkyl, 1-hydroxyalkyl, 2-hydroxyalkyl, 1-hydroxyhalogenalkyl, 1-alkenyl or 2-alkenyl, X1 represents fluorine, chlorine, bromine or iodine, X2 represents fluorine, chlorine, bromine or iodine, and Y represents nitrogen or a CH group, and addition products thereof with acids or metal salts are very active as microbicides in plant protection and in the protection of materials.

Substituted biphenyl oxazolines

The invention relates to new substituted biphenyloxazolines of the formula (I) STR1 in which R1 represents C1 -C6 -halogenoalkylthio and R2 represents hydrogen, or R1 and R2 together with the carbon atoms to which they are bonded form a halogen-substituted 5- or 6-membered heterocyclic ring, X represents hydrogen, halogen, C1 -C6 -alkyl or C1 -C6 -alkoxy, and m represents 0, 1 or 2, to processes for their preparation, to new intermediates, and to the use of the substituted biphenyloxazolines for combating animal pests, with the exception of the compound of the formula STR2

Acylated 5-aminopyrazoles and the use thereof to combat animal parasites

The present invention relates to new acylated 5-aminopyrazoles of the formula (I) STR1 in which R1, R2, R3, R4 and R5 have the meaning given in the description, to processes for their preparation and to their use as pesticides.

Substituted tetrahydro-5-nitro-pyrimidines

The present invention relates to novel substituted in that one tetrahydro-5-nitro-pyrimidine of the formula (I), according to claim 1, STR1 in which n, R1, R2 have the meaning given in the description, to a process for its preparation and to its use for combating animal pests, especially insects, arachnids and nematodes, which are encountered in agricultural, in forestry, in the protection of stored products and of materials and, in the hygiene sector.