Identification | Back Directory | [Name]
1-Propanol, 2-methyl-2-(methylamino)- | [CAS]
27646-80-6 | [Synonyms]
NSC 147612 2-Methyl-2-methylaminopropan-1-ol 2-methyl-2-(methylamino)-1-Propanol 2-(METHYLAMINO)-2-METHYL-1-PROPANOL N-Methyl-2-amino-2-methyl-1-propanol 1-Propanol, 2-methyl-2-(methylamino)- 2-methyl-2-(methylamino)propan-1-ol HCl 2-Methyl-2-(methylamino)propan-1-ol (~85%) N-(2-Hydroxy-1,1-dimethylethyl)-N-methylamine | [Molecular Formula]
C5H13NO | [MDL Number]
MFCD12184529 | [MOL File]
27646-80-6.mol | [Molecular Weight]
103.16 |
Chemical Properties | Back Directory | [Boiling point ]
162℃ | [density ]
0.878 | [Fp ]
62℃ | [storage temp. ]
2-8°C(protect from light) | [solubility ]
Chloroform (Slightly), Methanol (Slightly) | [form ]
Colourless Semi-Solid | [pka]
15.90±0.10(Predicted) | [Appearance]
White to light brown Solid-liquid mixture |
Hazard Information | Back Directory | [Uses]
2-Methyl-2-(methylamino)propan-1-ol functions as an antimicrobial agent for metal-working lubricant oils. | [Synthesis]
General procedure for the synthesis of 2-methyl-2-methylamino-1-propanol from 2-(Boc-amino)-2-methyl-1-propanol: tert-butyl 1-hydroxy-2-methylpropan-2-ylcarbamate (67 g, 354 mmol) was slowly added dropwise under nitrogen protection and at 0 °C to a tetrahydrofuran (THF) solution (150 mL) of LiAlH4 ( 40.3 g, 1062 mmol) in a tetrahydrofuran (THF) solution (400 mL) under stirring. The reaction mixture was stirred at 90 °C overnight and then cooled, followed by quenching by sequential addition of water (40.5 mL), 15% aqueous NaOH solution (40.5 mL) and water (40.5 mL) at 0 °C. The mixture was continued to be stirred for 1 hour and then filtered through diatomaceous earth. The organic layer was dried with sodium sulfate and concentrated in vacuum to give 2-methyl-2-methylamino-1-propanol (28 g, 77% yield) without further purification.LC-MS (ESI) analysis: m/z 104 [M + H]+; retention time 0.24 min. | [Toxics Screening Level]
Due to a lack of available information, the ITSL is being set at the default value of 0.1 μg/m3 with annual averaging. | [References]
[1] Patent: WO2014/114694, 2014, A1. Location in patent: Page/Page column 27-28 [2] Journal of the American Chemical Society, 1991, vol. 113, # 23, p. 8879 - 8886 [3] Patent: WO2010/103312, 2010, A1. Location in patent: Page/Page column 10 [4] Patent: WO2016/12916, 2016, A1. Location in patent: Page/Page column 29; 31 |
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