3,5-Dichlorophenylhydrazine hydrochloride
95%
- Product Code: 80279
Alias:
3,5-Dichlorophenylhydrazine hydrochloride
CAS:
63352-99-8
| Molecular Weight: | 213.49 g./mol | Molecular Formula: | C₆H₆Cl₂N₂HCl |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00012938 | |
| Melting Point: | 208-210 °C (dec.)(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various agrochemicals and pharmaceuticals. It is particularly valuable in the synthesis of herbicides and fungicides, where it contributes to the development of active ingredients that protect crops from pests and diseases. Additionally, it plays a role in the preparation of dyes and pigments, aiding in the creation of colorants for industrial applications. Its reactivity with carbonyl compounds makes it useful in the formation of hydrazone derivatives, which are further utilized in chemical research and development.
Product Specification:
| Test | Specification |
|---|---|
| CARBON | 31.7-35.8 |
| Melting point | 208-210 |
| WATER BY KARL FISCHER | 0-0.5 |
| PURITYHPLC | 95-100 |
| PURITYTITRATION WITH AGNO3 | 94.5-105.5 |
| APPEARANCE | WHITE TO PALE YELLOW SOLID |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $14.57 |
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| 5.000 | 10-20 days | $23.10 |
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| 25.000 | 10-20 days | $82.87 |
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| 100.000 | 10-20 days | $260.17 |
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3,5-Dichlorophenylhydrazine hydrochloride
Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various agrochemicals and pharmaceuticals. It is particularly valuable in the synthesis of herbicides and fungicides, where it contributes to the development of active ingredients that protect crops from pests and diseases. Additionally, it plays a role in the preparation of dyes and pigments, aiding in the creation of colorants for industrial applications. Its reactivity with carbonyl compounds makes it useful in the formation of hydrazone derivatives, which are further utilized in chemical research and development.
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