| Size | Price | Stock | Qty |
|---|---|---|---|
| 5g |
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| Other Sizes |
| Targets |
L-Alaninol does not have a specific biological target. Its primary function is as a chemical reagent and synthetic intermediate. As a chiral amino alcohol, it is used to introduce chirality into other molecules. Its in vitro and in vivo activity is not typically studied, as it is not intended for biological use.
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|---|---|
| ln Vitro |
Detailed in vitro biological activity data for L-Alaninol are not applicable, as it is a chemical reagent used primarily in organic synthesis. Its utility is demonstrated in the synthesis of various chiral compounds. Its purity and identity are confirmed using analytical techniques.
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| ln Vivo |
Detailed in vivo activity data for L-Alaninol are not applicable, as the compound is not intended for biological use. It is a research chemical used in synthetic organic chemistry.
|
| Enzyme Assay |
Non-cell-based assays for L-Alaninol are not applicable, as it is not a drug. Its identity and purity are assessed using standard analytical chemistry techniques, including HPLC, NMR, and mass spectrometry.
|
| Cell Assay |
Cellular assays for L-Alaninol are not applicable, as it is not a drug. It is not used in cell-based studies.
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| Animal Protocol |
In vivo animal models for L-Alaninol are not applicable, as it is not a drug. It is not used in animal studies.
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| ADME/Pharmacokinetics |
L-Alaninol has a molecular weight of 75.11 g/mol and a molecular formula of C₃H₉NO. Its CAS number is 2749-11-3. The compound is a colorless to pale yellow liquid. It is soluble in water and organic solvents. Purity is typically ≥98%. Storage conditions: room temperature, protected from moisture.
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| Toxicity/Toxicokinetics |
L-Alaninol is a chemical reagent with low toxicity. However, as a research chemical, standard laboratory safety precautions should be followed when handling it. It is for research use only and is not for human consumption.
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| Additional Infomation |
(S)-2-aminoprop-1-ol is a 2-aminoprop-1-ol with the S configuration. It is the conjugate base of (S)-2-aminoprop-1-ol (1+). It is the enantiomer of (R)-2-aminoprop-1-ol.
L-Alaninol is also known as (S)-2-Aminopropanol. It is a chiral amino alcohol used as a building block in organic synthesis, particularly for the preparation of chiral ligands and pharmaceuticals. Its CAS number is 2749-11-3. |
| Molecular Formula |
C3H9NO
|
|---|---|
| Molecular Weight |
75.111
|
| Exact Mass |
75.068
|
| CAS # |
2749-11-3
|
| Related CAS # |
L-Alaninol-d3;352438-84-7
|
| PubChem CID |
80307
|
| Appearance |
Colorless to light yellow liquid（Density：0.965 g/cm3）
|
| Density |
0.9±0.1 g/cm3
|
| Boiling Point |
174.5±0.0 °C at 760 mmHg
|
| Melting Point |
-2°C
|
| Flash Point |
83.9±0.0 °C
|
| Vapour Pressure |
0.4±0.7 mmHg at 25°C
|
| Index of Refraction |
1.440
|
| Source |
Originated from microorganisms
|
| LogP |
-0.96
|
| Hydrogen Bond Donor Count |
2
|
| Hydrogen Bond Acceptor Count |
2
|
| Rotatable Bond Count |
1
|
| Heavy Atom Count |
5
|
| Complexity |
22.9
|
| Defined Atom Stereocenter Count |
1
|
| SMILES |
O([H])C([H])([H])[C@]([H])(C([H])([H])[H])N([H])[H]
|
| InChi Key |
BKMMTJMQCTUHRP-VKHMYHEASA-N
|
| InChi Code |
InChI=1S/C3H9NO/c1-3(4)2-5/h3,5H,2,4H2,1H3/t3-/m0/s1
|
| Chemical Name |
(2S)-2-aminopropan-1-ol
|
| Synonyms |
L-Alaninol; 2-Aminopropanol
|
| HS Tariff Code |
2934.99.9001
|
| Storage |
Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month |
| Shipping Condition |
Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs)
|
| Solubility (In Vitro) |
DMSO: ~200 mg/mL (~2662.8 mM; with ultrasonication)
|
|---|---|
| Solubility (In Vivo) |
Solubility in Formulation 1: ≥ 5 mg/mL (66.57 mM) (saturation unknown) in 10% DMSO + 40% PEG300 + 5% Tween-80 + 45% Saline (add these co-solvents sequentially from left to right, and one by one), Clear solution.
For example, if 1 mL of working solution is to be prepared, you can add 100 μL of DMSO stock solution (50.0 mg/mL) to 400 μL of PEG300 and mix well; then add 50 μL of Tween-80 and mix well; finally add 450 μL of physiological saline and adjust the volume to 1 mL. Preparation of saline: Dissolve 0.9 g of sodium chloride in 100 mL ddH₂ O to obtain a clear solution. Solubility in Formulation 2: ≥ 5 mg/mL (66.57 mM) (saturation unknown) in 10% DMSO + 90% Corn Oil (add these co-solvents sequentially from left to right, and one by one), Clear solution. For example, if 1 mL of working solution is to be prepared, you can add 100 μL of DMSO stock solution (50.0 mg/mL) to 900 μL of corn oil and mix well. (Please use freshly prepared in vivo formulations for optimal results.) |
| Preparing Stock Solutions | 1 mg | 5 mg | 10 mg | |
| 1 mM | 13.3138 mL | 66.5690 mL | 133.1381 mL | |
| 5 mM | 2.6628 mL | 13.3138 mL | 26.6276 mL | |
| 10 mM | 1.3314 mL | 6.6569 mL | 13.3138 mL |
*Note: Please select an appropriate solvent for the preparation of stock solution based on your experiment needs. For most products, DMSO can be used for preparing stock solutions (e.g. 5 mM, 10 mM, or 20 mM concentration); some products with high aqueous solubility may be dissolved in water directly. Solubility information is available at the above Solubility Data section. Once the stock solution is prepared, aliquot it to routine usage volumes and store at -20°C or -80°C. Avoid repeated freeze and thaw cycles.
Calculation results
Working concentration： mg/mL；
Method for preparing DMSO stock solution： mg drug pre-dissolved in μL DMSO (stock solution concentration mg/mL). Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug.
Method for preparing in vivo formulation:：Take μL DMSO stock solution, next add μL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O，mix and clarify.
(1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
(2) Be sure to add the solvent(s) in order.
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