N-Benzylhydroxylamine hydrochloride
98%
- Product Code: 72893
Alias:
N-Benzyl Hydroxylamine Hydrochloride
CAS:
29601-98-7
| Molecular Weight: | 159.61 g./mol | Molecular Formula: | C₇H₉NOHCl |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00043377 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, sealed |
Product Description:
N-Benzylhydroxylamine hydrochloride is widely used in organic synthesis as a versatile reagent. It serves as a key intermediate in the preparation of various pharmaceuticals, particularly in the synthesis of antibiotics and antifungal agents. The compound is also employed in the development of chelating agents, which are useful in metal ion sequestration and detoxification processes. Additionally, it plays a role in the production of oximes, which are important in the manufacture of agrochemicals and as protective groups in peptide synthesis. Its application extends to research laboratories where it is utilized in the study of reaction mechanisms and the development of novel organic compounds.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 98 100% |
| Melting point | 100 115? |
| APPEARANCE | White crystalline powder |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿360.00 |
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| 5.000 | 10-20 days | ฿450.00 |
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| 25.000 | 10-20 days | ฿600.00 |
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| 100.000 | 10-20 days | ฿1,740.00 |
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| 500.000 | 10-20 days | ฿7,350.00 |
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N-Benzylhydroxylamine hydrochloride
N-Benzylhydroxylamine hydrochloride is widely used in organic synthesis as a versatile reagent. It serves as a key intermediate in the preparation of various pharmaceuticals, particularly in the synthesis of antibiotics and antifungal agents. The compound is also employed in the development of chelating agents, which are useful in metal ion sequestration and detoxification processes. Additionally, it plays a role in the production of oximes, which are important in the manufacture of agrochemicals and as protective groups in peptide synthesis. Its application extends to research laboratories where it is utilized in the study of reaction mechanisms and the development of novel organic compounds.
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