| Company Name: |
TianJin Alta Scientific Co., Ltd.
|
| Tel: |
022-65378550-8551 |
| Email: |
contact@altascientific.com |
| Products Intro: |
Product Name:Fenoprop-isooctyl ester
CAS:32534-95-5
Purity:98% Package:10Mg 25Mg 100Mg
|
| Company Name: |
Alta Scientific Co., Ltd.
|
| Tel: |
022-6537-8550 15522853686 |
| Email: |
sales@altasci.com.cn |
| Products Intro: |
Product Name:Fenoprop-isooctyl ester
CAS:32534-95-5
Purity:99% Package:10mg;100mg;1g
|
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| | FENOPROP-ISOOCTYL ESTER Basic information |
| Product Name: | FENOPROP-ISOOCTYL ESTER | | Synonyms: | 2,4,5-trichlorophenoxypropionicacidester;FENOPROP-ISOOCTYL ESTER;2-(2,4,5-trichlorophenoxy)-propanoicaciisooctylester;2-(2,4,5-trichlorophenoxy)propionicacidisooctylester;2-(2,4,5-trichlorophenoxy)-propionicaciisooctylester;isooctyl 2-(2,4,5-trichlorophenoxy)propionate;6-methylheptyl 2-(2,4,5-trichlorophenoxy)propanoate;4-methylheptyl2-(2,4,5-trichlorophenoxy)propanoate | | CAS: | 32534-95-5 | | MF: | C17H23Cl3O3 | | MW: | 381.72172 | | EINECS: | 251-085-8 | | Product Categories: | | | Mol File: | 32534-95-5.mol |  |
| | FENOPROP-ISOOCTYL ESTER Chemical Properties |
| | FENOPROP-ISOOCTYL ESTER Usage And Synthesis |
| Production Methods | Fenoprop-isoctyl was produced through a classic “ester of an ester” route that mirrored other phenoxy herbicide derivatives of its era. Manufacturers began with technical-grade fenoprop, itself obtained by chlorinating and then etherifying the appropriate phenolic precursor to install the 2-propyl side chain. Once purified, this phenoxy acid was esterified with iso-octanol under controlled, typically acid-catalysed conditions, using heat and continuous water removal to drive the reaction forward while avoiding decomposition of the phenoxy structure. | | General Description | White solids. Primary hazard is to threat to the environment. Immediate steps should be taken to limit spread to the environment. Burn, though may be difficult to ignite. Used as herbicides and plant growth regulators. | | Air & Water Reactions | Slightly soluble in water. | | Reactivity Profile | Esters react with acids to liberate heat along with alcohols and acids. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Heat is also generated by the interaction of esters with caustic solutions. Flammable hydrogen is generated by mixing esters with alkali metals and hydrides. | | Health Hazard | INHALATION: Vapors or mists may be irritating to nose and throat. EYES: Mild irritation. SKIN: Irritation-slight to moderate. INGESTION: Weakness, lethargy, anorexia, diarrhea, spasticity, possible death due to ventricular fibrillation and subsequent cardiac arrest. | | Mechanism of action | Synthetic auxin affecting nucleic acid biosynthesis and cell elongation. Systemic, selective. | | Pesticide Type | Herbicide; Plant Growth Regulator |
| | FENOPROP-ISOOCTYL ESTER Preparation Products And Raw materials |
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