Methoxyamine hydrochloride
25-30 wt. % aqueous solution
- Product Code: 122949
Alias:
Methoxyamine hydrochloride
O-methylhydroxylamine hydrochloride
CAS:
593-56-6
| Molecular Weight: | 83.52 g./mol | Molecular Formula: | CH₅NOHCl |
|---|---|---|---|
| EC Number: | 209-798-7 | MDL Number: | MFCD00012951 |
| Melting Point: | 151-154 °C(lit.) | Boiling Point: | 105-110°C |
| Density: | 1.1 g/mL at 25 °C | Storage Condition: | Room temperature, dry, sealed |
Product Description:
Methoxyamine hydrochloride is widely used in organic synthesis as a reagent for the protection of carbonyl groups. It reacts with aldehydes and ketones to form oxime derivatives, which are stable under various reaction conditions, allowing further transformations without affecting the carbonyl functionality. This property makes it valuable in the synthesis of complex molecules, including pharmaceuticals and natural products. Additionally, it is employed in the modification of nucleic acids, particularly in the preparation of oligonucleotides for research and therapeutic applications. Its ability to form stable adducts with DNA bases also makes it useful in studies related to DNA damage and repair mechanisms.
Product Specification:
| Test | Specification |
|---|---|
| Concentration | 25-30 |
| Infrared Spectrum | Conforms To Structure |
| Appearance | Colorless To Yellow Liquid |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | £7.46 |
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| 25.000 | 10-20 days | £11.08 |
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| 100.000 | 10-20 days | £24.88 |
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| 500.000 | 10-20 days | £96.35 |
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Methoxyamine hydrochloride
Methoxyamine hydrochloride is widely used in organic synthesis as a reagent for the protection of carbonyl groups. It reacts with aldehydes and ketones to form oxime derivatives, which are stable under various reaction conditions, allowing further transformations without affecting the carbonyl functionality. This property makes it valuable in the synthesis of complex molecules, including pharmaceuticals and natural products. Additionally, it is employed in the modification of nucleic acids, particularly in the preparation of oligonucleotides for research and therapeutic applications. Its ability to form stable adducts with DNA bases also makes it useful in studies related to DNA damage and repair mechanisms.
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