Weight | 47.057 g/mol |
---|---|
Formula | CH5NO |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 1 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
O-METHYLHYDROXYLAMINE (61038-31-1, 67-62-9)
methoxyamine · methoxylamine · methoxyamine hydrochloride
Score:
#1489 in Physics
,
#1496 in Biochemistry
,
#4389 in Chemistry
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- A new approach to the study of the base-excision repair pathway using methoxyamine. (Journal of Biological Chemistry, 1985)
- Therapeutic impact of methoxyamine: blocking repair of abasic sites in the base excision repair pathway. (Current opinion in investigational drugs, 2004)
- Methoxyamine potentiates DNA single strand breaks and double strand breaks induced by temozolomide in colon cancer cells (Mutation Research-dna Repair, 2001)
- Modification of cytidine residues with a bisulfiteO-methylhydroxylamine mixture (Biochimica et Biophysica Acta, 1974)
- Reaction of apurinic/apyrimidinic sites with [14C]methoxyamine: A method for the quantitative assay of AP sites in DNA (Biochimica et Biophysica Acta, 1983)
- O-(2,3,4,5,6-pentafluorophenyl)methylhydroxylamine hydrochloride : a versatile reagent for the determination of carbonyl-containing compounds (Journal of Chromatography A, 1992)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - methoxyamine
- methoxylamine
- methoxyamine hydrochloride
-
SMILESCON
-
InChIKeyGMPKIPWJBDOURN-UHFFFAOYSA-N
- Pubchem - O-METHYLHYDROXYLAMINE
- Wikipedia - methoxyamine
Methoxyamine is the organic compound with the formula CH3ONH2. Also called O-methylhydroxylamine, it a colourless volatile liquid that is soluble in polar organic solvents and in water. It is a derivative of hydroxylamine with the hydroxyl hydrogen replaced by a methyl group.
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