IMINOCTADINE TRIACETATE Property

vapor pressure 

<0.4 x 10^-3 Pa (23 °C)

storage temp. 

0-6°C

pka

>9, >13, >13 (strong base)

Water Solubility 

764,000 mg l^-1 (25 °C)

Safety

RIDADR 

2588

HazardClass 

6.1(a)

PackingGroup 

I

Hazard and Precautionary Statements (GHS)

IMINOCTADINE TRIACETATE Chemical Properties,Usage,Production

Uses

Iminoctadine triacetate is used as a seed treatment or spray for control of Septoriu nodorum, Tilletia caries, Fusarium spp. and Helminthosporium spp. in cereals. It is also used on citrus fruit and apples.

Definition

ChEBI: Iminoctadine acetate is a polymer.

Metabolic pathway

Iminoctadine is a strong base with two guanidino groups with pKa >13 and an amino group with pKa >9. It is ionised at all pH values typically encountered in the environment. Although the tri-cation is highly polar it will be strongly sorbed to soils by the ion exchange mechanism as well as by hydrophobic interactions of its alkyl chains. Amino compounds usually readily form unextractable residues in soils. For these reasons the fungicide is strongly sorbed to soils and there it has low biological availability to plants and animals and is protected from microbial degradation. The only major identified products of transformation were products of photooxidation and the deamidinated products detected in rats.

Degradation

Iminoctadine triacetate is stable in neutral and aqueous acidic media but unstable in alkaline conditions. There was no appreciable hydroysis of iminoctadine in buffer solutions at pH 5,7 and 9 after one month at 25 °C (PM). [¹⁴C-guanidine]Iminoctadinetr iacetate was coated onto glass plates and exposed to artificial (12 hours day^-1) or natural sunlight. Loss by volatilisation was negligible over 336 hours. Photodegradation was initially rapid (DT₅₀ 40 hours) but subsequently slowed (DT₅₀ 912 hours). One major and several minor photoproducts were detected after irradiation for 336 hours and in total represented 69% of the applied radioactivity of which the major product accounted for 31%. The major metabolite was converted into pyrimidine derivatives to aid analysis by IR, NMR and MS methods. The major photoproduct was tentatively identified as 4- or 6-methyl-5-oxo-9-azaheptadecane-1,17-diguanidine (2 or 3, Scheme 1) and it was formed by photo-oxidation and methylation of adjacent methylene groups. One of the intermediates in the formation of 2 or 3 was another unidentified photo-oxidation product of iminoctadine (Sato et al., 1985b).