- Naftalofos
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- $30.00
-
2025-04-15
- CAS:1491-41-4
- Min. Order: 1kg
- Purity: 99%
- Supply Ability: 5000kg/week
- Naftalofos
-
- $1.00
-
2019-07-06
- CAS:1491-41-4
- Min. Order: 1KG
- Purity: 99%
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| | Naftalofos Basic information |
| Product Name: | Naftalofos | | Synonyms: | e9002;ent25,567;Phosphoric acid, 1,3-dioxo-1H-benz[de]isoquinolin-2(3H)-yl diethyl ester;phosphoric acid (1,3-dioxo-2-benzo[de]isoquinolinyl) diethyl ester;Phosphoric acid, N-hydroxynaphthalimide O,O-diethyl ester;maretin;n-hydroxy-naphthalimiddiethylphosphate;n-hydroxynaphthylimidediethylphosphate | | CAS: | 1491-41-4 | | MF: | C16H16NO6P | | MW: | 349.28 | | EINECS: | 216-078-6 | | Product Categories: | | | Mol File: | 1491-41-4.mol |  |
| | Naftalofos Chemical Properties |
| Melting point | 174-179° | | storage temp. | 0-6°C | | solubility | DMSO (Slightly), Ethyl Acetate (Slightly) | | form | solid | | Boiling point | 487.3±28.0 °C(Predicted) | | density | 1.41±0.1 g/cm3(Predicted) | | CAS DataBase Reference | 1491-41-4(CAS DataBase Reference) | | EPA Substance Registry System | Naftalofos (1491-41-4) |
| Hazard Codes | T | | Risk Statements | 24/25 | | Safety Statements | 36/37-45 | | RIDADR | 2783 | | WGK Germany | 3 | | RTECS | QK5775000 | | HazardClass | 6.1(b) | | PackingGroup | III | | Toxicity | chicken,LD50,oral,43300ug/kg (43.3mg/kg),PERIPHERAL NERVE AND SENSATION: FLACCID PARALYSIS WITHOUT ANESTHESIA (USUALLY NEUROMUSCULAR BLOCKAGE)BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLDBEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY),Toxicology and Applied Pharmacology. Vol. 11, Pg. 49, 1967. |
| | Naftalofos Usage And Synthesis |
| Uses | Anthelmintic(veterinary). | | Definition | ChEBI: Naftalofos is an organic heterotricyclic compound. It has a role as an anthelminthic drug. | | Brand name | Maretin (Bayer Animal Health). | | Synthesis | Naftalofos is synthesised through a multi-step chemical process that
begins with the preparation of O-ethyl phenylphosphonothioic acid, which
serves as the phosphorus-containing core. This intermediate is then
reacted with 2-naphthol, a hydroxylated aromatic compound, via
esterification, forming the characteristic O-naphthyl linkage. After the
coupling step, the crude product undergoes purification to isolate. |
| | Naftalofos Preparation Products And Raw materials |
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