L-Alaninol-d3
Based on 1 Customer Validation
L-Alaninol-d3 ((S)-2-Amino-1-propanol-d3; (S)-2-Aminopropanol-d3; (S)-Alaninol-d3) is the deuterated-labeled L-Alaninol (HY-Y0837). L-Alaninol ((S)-2-Amino-1-propanol; (S)-2-Aminopropanol; (S)-Alaninol) is a chiral amino alcohol that serves as a precursor for Levofloxacin (HY-B0330) and Metolachlor (HY-B1871). L-Alaninol acts as the sole carbon source for Pseudomonas sp. strain KIE171, and it is a metabolite produced by the hydrolysis of γ-glutamyl-L-alaninol. L-Alaninol functions as a substrate for oxidative/deaminative degradation and undergoes enzymatic glutamylation via IpuC. It is used as a synthetic building block in the fields of agriculture, pharmaceuticals, and peptide chemistry, and also serves as a chiral auxiliary.
For research use only. We do not sell to patients.
- Purity: 98.0%
- CAS No.: 352438-84-7
- Formula: C3H6D3NO
- Molecular Weight:78.13
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Storage:Pure form -20°C, 3 years ; In solvent -80°C, 6 months , -20°C, 1 month
Biological Activity
1. This compound can be used as a tracer
2. This compound can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
Chemical Information
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CAS No. 352438-84-7
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Unlabeled Cas 2749-11-3
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Appearance Liquid (Density: 0.943±0.06 g/cm3)
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Molecular Weight 78.13
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Formula C3H6D3NO
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Color Colorless to light yellow
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SMILES
OC[C@@H](N)C([2H])([2H])[2H]
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Synonyms
(S)-2-Amino-1-propanol-d3; (S)-2-Aminopropanol-d3; (S)-Alaninol-d3
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Pure form -20°C 3 years In solvent -80°C 6 months -20°C 1 month
Purity & Documentation
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Data Sheet (268 KB)
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SDS (393 KB)
- English - EN (393 KB)
- Français - FR (393 KB)
- Deutsch - DE (393 KB)
- Norwegian - NO (393 KB)
- Español - ES (393 KB)
- Swedish - SV (393 KB)
- Italian - IT (393 KB)
- Korean - KR (393 KB)
- Portuguese - PT (393 KB)
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Handling Instructions (2659 KB)
References
[1]. Benninghaus L, et al. γ-Glutamylation of Isopropylamine by Fermentation. Chembiochem : a European journal of chemical biology. 2024 Jan 15;25(2):e202300608. [Content Brief]
[2]. de Azevedo Wäsch SI, et al. Transformation of isopropylamine to L-alaninol by Pseudomonas sp. strain KIE171 involves N-glutamylated intermediates. Applied and environmental microbiology. 2002 May;68(5):2368-75. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
- L-Alaninol-d3
- 352438-84-7
- (S)-2-Amino-1-propanol-d3
- (S)-2-Aminopropanol-d3
- (S)-Alaninol-d3
- Isotope-Labeled Compounds
- Biochemical Assay Reagents
- Drug Intermediate
- L-alanine
- isopropylamine
- γ-glutamylamide synthetase
- L-2-aminopropionaldehyde
- Pseudomonas sp. strain KIE171
- γ-glutamyl-L-alaninol
- propionaldehyde
- γ-glutamylamide hydrolase
- IpuC
- propionic acid
- Inhibitor
- inhibitor
- inhibit