| Identification | Back Directory | [Name]
DL-ALPHA-(METHYLAMINOMETHYL)BENZYL ALCOHOL | [CAS]
6589-55-5 | [Synonyms]
win5529-2
HALOSTACHINE
N-METHYLPHENYLETHANOLAMINE
2-METHYLAMINO-1-PHENYLETHANOL
2-(methylamino)-1-phenyl-ethano
alpha-(methylamino)benzylalcohol
α-(methylaminomethyl)benzyl alcohol
dl-à-(methylaminomethyl)benzyl alcohol
α-[(Methylamino)methyl]benzenemethanol
ALPHA-(METHYLAMINOMETHYL)BENZYL ALCOHOL
alpha-((methylamino)methyl)-benzylalcoho
DL-ALPHA-(METHYLAMINOMETHYL)BENZYL ALCOHOL
DL-ɑ-(Methylaminomethyl)benzyl alcohol, 99%
DL-^a-(Methylaminomethyl)benzyl alcohol, 99%
Halostachine~2-(Methylamino)-1-phenylethanol
2-(Methylamino)-1-phenylethanol alpha-(Methylaminomethyl)benzyl alcohol | [EINECS(EC#)]
229-525-5 | [Molecular Formula]
C9H13NO | [MDL Number]
MFCD00004506 | [MOL File]
6589-55-5.mol | [Molecular Weight]
151.21 |
| Chemical Properties | Back Directory | [Appearance]
white crystals | [Melting point ]
74-76 °C(lit.)
| [Boiling point ]
132-133 °C(Press: 15 Torr) | [density ]
1.02 g/cm3(Temp: 0 °C) | [storage temp. ]
2-8°C | [solubility ]
Chloroform (Slightly), Methanol (Slightly) | [form ]
Fine Crystalline Needles | [pka]
14.03±0.20(Predicted) | [color ]
White | [Stability:]
Stable. Incompatible with acids, acid chlorides, acid anhydrides, oxidizing agents. | [Merck ]
14,4601 | [BRN ]
1072841 | [InChI]
InChI=1S/C9H13NO/c1-10-7-9(11)8-5-3-2-4-6-8/h2-6,9-11H,7H2,1H3 | [InChIKey]
ZCTYHONEGJTYQV-UHFFFAOYSA-N | [SMILES]
C(C1C=CC=CC=1)(O)CNC |
| Hazard Information | Back Directory | [Chemical Properties]
white crystals | [Uses]
α-(Methylaminomethyl)benzyl alcohol was used in the synthesis of 1,4-disubstituted-2,3,4,5-tetrahydro-1H-3-benzazepines. It was also used as internal standard during determination of pseudoephedrine and phenylpropanolamine urine concentrations by HPLC. | [Definition]
ChEBI: N-methylphenylethanolamine is an alkaloid that is ethanolamine having the phenyl group at the 1-position and a methyl group attached to the nitrogen. It has been isolated from Halostachys caspica. It has a role as a human metabolite and a plant metabolite. It is an alkaloid and a member of phenylethanolamines. It is a conjugate base of a N-methylphenylethanolaminium. | [General Description]
α-(Methylaminomethyl)benzyl alcohol is a potential substrate for studies involving phenylethanolamine-N-methyltransferase. |
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