Tebuconazole(CAS#107534-96-3)
Chemical Property:
107534-96-3 – Names and Identifiers
107534-96-3 – Physico-chemical Properties
| Molecular Formula | C16H22ClN3O |
| Molar Mass | 307.82 |
| Density | 1.14g/cm3 |
| Melting Point | 102-105 ºC |
| Boling Point | 475.4°C at 760 mmHg |
| Flash Point | 241.3°C |
| Water Solubility | 32 MG/L AT 20 ºC |
| Solubility | At 20°C, water 32mg/L(pH 7), dichloromethane> 200g/L, hexane <0.1g/L, isopropanol, toluene 50~100g/L. |
| Vapor Presure | 7.6E-10mmHg at 25°C |
| Appearance | Colorless crystal |
| Color | White to almost white powder to crystal |
| Storage Condition | 2-8℃ |
| Refractive Index | 1.564 |
| MDL | MFCD00145350 |
| Physical and Chemical Properties | melting point 102.4°C water-soluble 32 mg/L at 20°C |
| Use | Triazole fungicides, highly effective fungicides for seed treatment or foliar spraying of important cash crops, can effectively control various rust diseases of cereal crops, etc. |
107534-96-3 – Risk and Safety
| Hazard Symbols | Xn – Harmful N – Dangerous for the environment  |
| Risk Codes | R22 – Harmful if swallowed R51/53 – Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment. R63 – Possible risk of harm to the unborn child |
| Safety Description | S2 – Keep out of the reach of children. S22 – Do not breathe dust. S36/37 – Wear suitable protective clothing and gloves. S61 – Avoid release to the environment. Refer to special instructions / safety data sheets. |
107534-96-3 – Reference
| Reference
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1. Xiao Suping, Zhong Rongrong, Gao Hui, et al. Rapid Determination of Eight Pesticide Residues in Different Dendrobium … |
107534-96-3 – Introduction Tebuconazole is an organic compound with the chemical name 5-hydroxymethyloxazolidin-4-one.
Tebuconazole is a white solid with good water solubility and thermal stability. It is an amphoteric substance and can form hydrochloride or hydroxide in water. Tebuconazole has two common enantiomers: levorotatory L-tebuconazole and dextrorotatory D-tebuconazole.
As a ketol antibiotic, it can inhibit the growth of various bacteria, such as Staphylococcus aureus and Escherichia coli.
Tebuconazole can be synthesized via a series of routes. One commonly used method is the reaction of acetoacetate with hydrazine to generate the ketol imine of tebuconazole, followed by acidic hydrolysis to obtain tebuconazole.
It may release toxic gases under high temperature. Keep away from fire sources and high-temperature environments. Contact with eyes and skin may cause irritation and allergic reactions; proper protective measures shall be taken. Waste shall be disposed of in accordance with local regulations.
