Tridemorph 96%TC/86%OL/75%EC/3%DS-fungicide

Specifications

Tridemorph 96%TC/86%OL/75%EC/75%SL/3%DS
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Detailed Product Description

 

Tridemorph 96%TC(technical)

Tridemorph 96%TC/86%OL/75%EC/75%SL/3%DS

 

Common name

tridemorph (BSI, E-ISO);

 

IUPAC name

4-alkyl-2,6-dimethylmorpholine; for original definition, 2,6-dimethyl-4-tridecylmorpholine

Chemical Abstracts name

for original structure/main component, 2,6-dimethyl-4-tridecylmorpholine

 

CAS RN [81412-43-3] new definition; [24602-86-6] 4-tridecyl- component

Formulation types: EC.

Molecular formula: C19H39NO (approx.)

Molecular weight: 297.5 (approx.) 

Properties: Yellow, oily liquid, with a slight amine-like odour.

 

 

Toxicity:

Oral	Acute oral LD50 for rats 480 mg/kg.
Skin and eye	Acute percutaneous LD50 for rats >4000 mg/kg. Skin irritant; not an eye irritant (rabbits).
Inhalation	LC50 (4 h) for rats 4.5 mg/l air.
NOEL	(2 y) for rats 30 mg/kg diet (c. 1.8 mg/kg daily), for dogs 50 ppm diet.
ADI	0.016 mg/kg b.w.
Toxicity class	WHO (a.i.) II; EPA (formulation) III
EC hazard	R61| Xn; R20/22| Xi; R38| N; R50, R53 (for 4-tridecyl- component)

 

 

 

Applications:

Biochemistry	Ergosterol biosynthesis inhibitor, by inhibition of steroid reduction (sterol-D14-reductase) and isomerisation (D8 to D7-isomerase).
Mode of action	Systemic fungicide with eradicant action. Absorbed by the leaves and roots, giving some protective action.
Uses	Control of Erysiphe graminis in cereals, Mycosphaerella spp. in bananas, Corticium salmonicolor and Exobasidium vexans in tea, and Oidium heveae in hevea. Mixed with carbendazim to extend spectrum of cereal diseases controlled.
Phytotoxicity	Scorch may occur on some winter wheat varieties under certain climatic conditions.

 

 

 

Packing:

According to the customers' request