| Identification | Back Directory | [Name]
ISOPROPALIN | [CAS]
33820-53-0 | [Synonyms]
EL-179
Paarlan
PAARLAN(R)
ISOPROPALIN
isopropaline
Isopropalin 0
ISOPROPALIN STANDARD
ISOPROPALIN, 1GM, NEAT
Isopropalin 1g [33820-53-0]
ISOPROPALIN ISO 9001：2015 REACH
isopropalin (bsi,iso,ansi,wssa)
2,6-dinitro-n,n-dipropyl-cumidin
2,6-dinitro-n,n-dipropylcumidine
(DG) Isopropalin 1g [33820-53-0]
Isopropalin @100 μg/mL in Methanol
Isopropalin@1000 μg/mL in Methanol
Cumidine, 2,6-dinitro-N,N-dipropyl-
2,6-DINITRO-N,N-DI-N-PROPYL CUMIDINE
ISOPROPALIN PESTANAL (4-ISOPROPYL- 2,6-D
Isopropalin Solution in Methanol, 1000μg/mL
2,6-dinitro-n,n-dipropyl-4-isopropylaniline
2,6-dinitro-n,n-dipropyl-p-isopropyl-anilin
4-ISO-PROPYL-2,6-DINITRO-N,N-DIPROPYLANILINE
2,6-dinitro-4-propan-2-yl-N,N-dipropylaniline
2,6-DINITRO-N,N-DIROPYL-PARA-ISOPROPYLANILINE
4-Isopropyl-2,6-dinitro-N,N-dipropylbenzenamine
N-(4-Isopropyl-2,6-dinitrophenyl)-N,N-dipropylamine
4-(1-methylethyl)-2,6-dinitro-n,n-dipropyl-benzenamin
4-(1-methylethyl)-2,6-dinitro-n,n-dipropylbenzenamine
Benzenamine, 4-(1-methylethyl)-2,6-dinitro-N,N-dipropyl- | [EINECS(EC#)]
251-690-7 | [Molecular Formula]
C15H23N3O4 | [MDL Number]
MFCD00055306 | [MOL File]
33820-53-0.mol | [Molecular Weight]
309.36 |
| Chemical Properties | Back Directory | [Boiling point ]
449.64°C (rough estimate) | [density ]
1.1220 (rough estimate) | [refractive index ]
1.5600 (estimate) | [Fp ]
40 °C | [storage temp. ]
0-6°C | [form ]
Liquid | [pka]
1.27±0.50(Predicted) | [Water Solubility ]
0.1mg/L(25 ºC) | [BRN ]
2762577 | [Henry's Law Constant]
1.9×10-1 mol/(m3Pa) at 25℃, Mackay et al. (2006) | [InChI]
1S/C15H23N3O4/c1-5-7-16(8-6-2)15-13(17(19)20)9-12(11(3)4)10-14(15)18(21)22/h9-11H,5-8H2,1-4H3 | [InChIKey]
NEKOXWSIMFDGMA-UHFFFAOYSA-N | [SMILES]
CCCN(CCC)c1c(cc(cc1[N+]([O-])=O)C(C)C)[N+]([O-])=O | [EPA Substance Registry System]
Isopropalin (33820-53-0) |
| Hazard Information | Back Directory | [Uses]
Herbicide. | [Definition]
ChEBI: Isopropalin is a C-nitro compound. | [Production Methods]
The industrial production of isopropalin begins with the nitration of an aromatic ring, typically a substituted aniline, to introduce nitro groups at the 2 and 6 positions. This step is followed by alkylation to add an isopropyl group at the 4-position, enhancing the herbicide’s lipophilicity and soil-binding properties. The nitro groups are then reduced to amines, which are subsequently dialkylated using propyl halides to form the final compound, which is subsequently purified through solvent extraction and crystallisation to ensure high chemical purity. | [Mechanism of action]
Selective. Inhibition of microtubular assembly | [Pesticide Type]
Herbicide |
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