4-Hydrazinobenzoic acid
98%
- Product Code: 80423
Alias:
p-Carboxylphenylhydrazine; 4-hydrazinobenzoic acid, p-hydrazinobenzoic acid
CAS:
619-67-0
| Molecular Weight: | 152.15 g./mol | Molecular Formula: | C₇H₈N₂O₂ |
|---|---|---|---|
| EC Number: | 210-609-5 | MDL Number: | MFCD00007581 |
| Melting Point: | 218 °C (dec.)(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
Used as a key intermediate in the synthesis of various pharmaceuticals, particularly in the production of drugs targeting cardiovascular diseases and cancer. It plays a role in the development of hydrazide derivatives, which are explored for their antimicrobial and anti-inflammatory properties. Additionally, it is utilized in organic synthesis for the preparation of dyes and pigments, contributing to the coloration of textiles and materials. Its hydrazine group makes it valuable in chemical reactions such as condensation and coupling processes, enabling the creation of complex organic compounds.
Product Specification:
| Test | Specification |
|---|---|
| PURITY HPLC | 98 100% |
| Melting point | 205 219? |
| APPEARANCE | FAINT YELLOW TO BEIGE POWDER,CRYSTALS AND/OR CHUNKS |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿320.00 |
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| 25.000 | 10-20 days | ฿890.00 |
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| 100.000 | 10-20 days | ฿3,190.00 |
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| 500.000 | 10-20 days | ฿13,880.00 |
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4-Hydrazinobenzoic acid
Used as a key intermediate in the synthesis of various pharmaceuticals, particularly in the production of drugs targeting cardiovascular diseases and cancer. It plays a role in the development of hydrazide derivatives, which are explored for their antimicrobial and anti-inflammatory properties. Additionally, it is utilized in organic synthesis for the preparation of dyes and pigments, contributing to the coloration of textiles and materials. Its hydrazine group makes it valuable in chemical reactions such as condensation and coupling processes, enabling the creation of complex organic compounds.
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