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ChemicalBook--->CAS DataBase List--->81412-43-3

81412-43-3

81412-43-3 Structure

81412-43-3 Structure
IdentificationBack Directory
[Name]

TRIDEMORPH
[CAS]

81412-43-3
[Synonyms]

CALIXIN
bas2203f
tridemorf
Calixin(TM)
Tridemorphe
Tridemorf [czech]
tridemorph (bsi,iso)
Tridemorph (Mix of Isomers)
dimethyl-2,6tridecyl-4morpholine
Dimethyl-2,6 tridecyl-4 morpholine [french]
[EINECS(EC#)]

617-232-9
[Molecular Formula]

C19H39NO
[MDL Number]

MFCD00055522
[MOL File]

81412-43-3.mol
[Molecular Weight]

297.52
Chemical PropertiesBack Directory
[vapor pressure ]

1.2 x 10-2 Pa (20 °C)
[pka]

6.5
[Water Solubility ]

n = 10-12,11.7 mg l-1 (pH 7 at 20 °C)
[CAS DataBase Reference]

81412-43-3
[EPA Substance Registry System]

Tridemorph (81412-43-3)
Safety DataBack Directory
[HS Code ]

29349990
[Toxicity]

oth-mmo-omi 100 mmol/L NNGADV 5,69,80
Hazard InformationBack Directory
[Uses]

Tridemorph is a systemic fungicide which provides effective eradicant and protective control of powdery mildews, rusts and leaf blotch in cereals (especially caused by Evisyphe graminis) and in bananas.
[Definition]

ChEBI: 2,6-dimethyl-4-tridecylmorpholine is a member of the class of morpholines that is 2,6-dimethylmorpholine in which the hydrogen attached to the nitrogen is replaced by a tridecyl group. The configuration at positions 2 and 6 is unknown or unspecified. It has a role as an antifungal agrochemical. It is a member of morpholines and a tertiary amino compound.
[Safety Profile]

Moderately toxic by ingestion andskin contact. An experimental teratogen. Mutation datareported. When heated to decomposition it emits toxicfumes of NOx.
[Metabolic pathway]

Limited information is available to describe the degradation and metabolic fate of tridemorph. Hydroxylation of the tridecyl side-chain and the hydroxylation/oxidation of one of the methyl moieties in the morpholine ring were the primary metabolic reactions in animals (Scheme 1).
[Degradation]

Tridemorph (1) is stable to hydrolytic degradation (<50 °C). It degraded rapidly after being exposed to UV light with a half-life (DT50) of 16.5 hours (PM).
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