- TRIDEMORPH
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- $0.00 / 25KG
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2023-06-20
- CAS:81412-43-3
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 50000KG/month
- TRIDEMORPH
-
- $10.00 / 1KG
-
2021-08-25
- CAS:81412-43-3
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 10 mt
- TRIDEMORPH
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- $15.00 / 1KG
-
2021-08-12
- CAS:81412-43-3
- Min. Order: 1KG
- Purity: 99%+ HPLC
- Supply Ability: Monthly supply of 1 ton
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| | TRIDEMORPH Basic information |
| Product Name: | TRIDEMORPH | | Synonyms: | bas2203f;dimethyl-2,6tridecyl-4morpholine;tridemorf;tridemorph (bsi,iso);Dimethyl-2,6 tridecyl-4 morpholine [french];Tridemorf [czech];Tridemorphe;Tridemorph (Mix of Isomers) | | CAS: | 81412-43-3 | | MF: | C19H39NO | | MW: | 297.52 | | EINECS: | 617-232-9 | | Product Categories: | | | Mol File: | 81412-43-3.mol |  |
| | TRIDEMORPH Chemical Properties |
| 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) |
| HS Code | 29349990 | | Toxicity | oth-mmo-omi 100 mmol/L NNGADV 5,69,80 |
| | TRIDEMORPH Usage And Synthesis |
| 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). |
| | TRIDEMORPH Preparation Products And Raw materials |
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