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(+/-)-2-Amino-1-propanol, 98%
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(+/-)-2-Amino-1-propanol, 98%
(+/-)-2-Amino-1-propanol, 98%
(+/-)-2-Amino-1-propanol, 98%
Thermo Scientific Chemicals

(+/-)-2-Amino-1-propanol, 98%

CAS: 6168-72-5 | C3H9NO | 75.11 g/mol
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Catalog number L03608.14
also known as L03608-14
Price (EUR)
173,00
Each
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Quantity:
25 g
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Price (EUR)
173,00
Each
Add to cart
Chemical Identifiers
CAS6168-72-5
IUPAC Name2-aminopropan-1-ol
Molecular FormulaC3H9NO
InChI KeyBKMMTJMQCTUHRP-UHFFFAOYNA-N
SMILESCC(N)CO
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear colorless to yellow
FormLiquid or viscous liquid
Refractive Index1.4485-1.4525 @ 20°C
Assay (GC)≥95.0%
DL-Alaninol has been used in the synthesis of N6-α-(I-hydroxypropyl) lysine, diastereomers of DL-β-amino alcohols, enantiopure and racemic samples of 2-methyl-N-tosylaziridine, (±)-3-(5-dimethylcarbamoyl-pent-1-enyl)-N-(2-hydroxy-1-methyl-ethyl)benzamide.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
DL-Alaninol has been used in the synthesis of N6-α-(I-hydroxypropyl) lysine, diastereomers of DL-β-amino alcohols, enantiopure and racemic samples of 2-methyl-N-tosylaziridine, (±)-3-(5-dimethylcarbamoyl-pent-1-enyl)-N-(2-hydroxy-1-methyl-ethyl)benzamide.

Solubility
Fully miscible in water.

Notes
Air sensitive & hygroscopic. Store under inert gas. Store away from oxidizing agents, air, water/ moisture.
RUO – Research Use Only

General References:

  1. J M Ingram; W A Wood. The role of lysine residues in the activity of 2-keto-3-deoxy-6-phosphogluconate aldolase. Journal of Biological Chemistry. 1965, 240, (11), 4146-4151.
  2. Ravi Bhushan; Rajender Kumar; Ravi Bhushan; Rajender Kumar. Reversed-phase high performance liquid chromatographic separation of diastereomers of beta-amino alcohols and microwave assisted synthesis of Marfey's reagent, its chiral variants and diastereomers. Journal of chromatography. A. 2009, 1216, (12), 2592-2596.