| Identification | Back Directory | [Name]
NITROTHAL-ISOPROPYL | [CAS]
10552-74-6 | [Synonyms]
KUMULAN
PALLINAL
Nirothale
BAS-30000
Nitrothal-isop
Einecs 234-139-5
Nitrothal-isopropy
NITROTHAL-ISOPROPYL
Nitrothale-isopropyl
Nitrothal-isopropyl Standard
Nitrothale-isopropyl [french]
nitrothal-isopropyl (bsi,iso)
DIISOPROPYL 5-NITROISOPHTHALATE
NITROTHAL-ISOPROPYL PESTANAL
5-nitro-isophthalicacidiisopropylester
NITROTHAL-ISOPROPYL (DIISOPROPYL 5-NITR&
Nitrothal-isopropyl 100 μg/mL in Methanol
Nitrothal-isopropyl@1000 μg/mL in Methanol
Isophthalic acid, 5-nitro-, diisopropyl ester
bis(1-methylethyl)5-nitro-1,3-benzenedicarboxylate
Nitrothal-isopropyl,Diisopropyl-5-nitroisophthalat
3-benzenedicarboxylicacid,5-nitro-bis(1-methylethyl)ester
1,3-Benzenedicarboxylic acid, 5-nitro-, bis(1-methylethyl) ester
1,3-Benzenedicarboxylic acid, 5-nitro-, 1,3-bis(1-methylethyl) ester | [EINECS(EC#)]
234-139-5 | [Molecular Formula]
C14H17NO6 | [MDL Number]
MFCD00055456 | [MOL File]
10552-74-6.mol | [Molecular Weight]
295.29 |
| Chemical Properties | Back Directory | [Melting point ]
65℃ | [Boiling point ]
397.9±22.0 °C(Predicted) | [density ]
1.210±0.06 g/cm3(Predicted) | [Fp ]
100 °C | [storage temp. ]
0-6°C | [form ]
neat | [Henry's Law Constant]
5.7×102 mol/(m3Pa) at 25℃, Ebert et al. (2023) | [Major Application]
agriculture
environmental | [InChI]
1S/C14H17NO6/c1-8(2)20-13(16)10-5-11(14(17)21-9(3)4)7-12(6-10)15(18)19/h5-9H,1-4H3 | [InChIKey]
VJAWBEFMCIINFU-UHFFFAOYSA-N | [SMILES]
CC(C)OC(=O)c1cc(cc(c1)[N+]([O-])=O)C(=O)OC(C)C |
| Hazard Information | Back Directory | [Uses]
Nitrothal-isopropyl is a pesticide. | [Definition]
ChEBI: Nitrothal-isopropyl is a nitrobenzoic acid, an isopropyl ester and a diester. | [Production Methods]
Nitrothal-isopropyl is commercially synthesised through esterification of 5-nitroisophthalic acid with isopropanol. The production process begins with the nitration of isophthalic acid to yield 5-nitroisophthalic acid, which is then purified and reacted with isopropanol in the presence of an acid catalyst, typically sulphuric acid or p-toluenesulfonic acid, to form the diisopropyl ester. This esterification is carried out under reflux conditions to ensure complete conversion and high yield. | [Mechanism of action]
Non-systemic with contact action. Inhibits fungal growth but exact mode of action is unclear | [Pesticide Type]
Fungicide |
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