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L-Proline, 99%, Thermo Scientific Chemicals
34.90€ - 421.00€
Chemical Identifiers
| CAS | 147-85-3 |
|---|---|
| Molecular Formula | C5H9NO2 |
| Molecular Weight (g/mol) | 115.13 |
| MDL Number | MFCD00064318 |
| InChI Key | ONIBWKKTOPOVIA-UHFFFAOYNA-N |
| Synonym | l-proline, proline, l---proline, s-pyrrolidine-2-carboxylic acid, 2-pyrrolidinecarboxylic acid, --proline, --s-proline, 2s-pyrrolidine-2-carboxylic acid, prolinum, h-pro-oh |
| PubChem CID | 145742 |
| ChEBI | CHEBI:17203 |
| IUPAC Name | (2S)-pyrrolidine-2-carboxylic acid |
| SMILES | OC(=O)C1CCCN1 |
| Product Code | Brand | Quantity | Price | Quantity & Availability | |||||
|---|---|---|---|---|---|---|---|---|---|
| Product Code | Brand | Quantity | Price | Quantity & Availability | |||||
|
11439512
|
Thermo Scientific Alfa Aesar
A10199.14 |
25 g |
34.90€
25g |
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|
11449512
|
Thermo Scientific Alfa Aesar
A10199.22 |
100 g |
111.00€
100g |
Please sign in to purchase this item. Need a web account? Register with us today! | |||||
|
11459512
|
Thermo Scientific Alfa Aesar
A10199.36 |
500 g |
421.00€
500g |
Please sign in to purchase this item. Need a web account? Register with us today! | |||||
Description
L-Proline is used as asymmetric catalysts in organic synthesis and asymmetric aldol cyclization. It is involved in the Michael addition of dimethyl malonate to alfa-beta-unsaturated aldehydes. It is a precursor of hydroxyproline in collagen. It is an active component of collagen and involved in the proper functioning of joints and tendons. It finds uses in pharmaceutical, biotechnological applications due to its osmoprotectant property. Further, it is used with ninhydrin in the chromatography.
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.
ApplicationsL-Proline is used as asymmetric catalysts in organic synthesis and asymmetric aldol cyclization. It is involved in the Michael addition of dimethyl malonate to alfa-beta-unsaturated aldehydes. It is a precursor of hydroxyproline in collagen. It is an active component of collagen and involved in the proper functioning of joints and tendons. It finds uses in pharmaceutical, biotechnological applications due to its osmoprotectant property. Further, it is used with ninhydrin in the chromatography.
Solubility
Soluble in water and ethanol. Insoluble in ether, butanol and isopropanol.
Notes
Hygroscopic. Incompatible with strong oxidizing agents.
Chemical Identifiers
| 147-85-3 | |
| 115.13 | |
| ONIBWKKTOPOVIA-UHFFFAOYNA-N | |
| 145742 | |
| (2S)-pyrrolidine-2-carboxylic acid |
| C5H9NO2 | |
| MFCD00064318 | |
| l-proline, proline, l---proline, s-pyrrolidine-2-carboxylic acid, 2-pyrrolidinecarboxylic acid, --proline, --s-proline, 2s-pyrrolidine-2-carboxylic acid, prolinum, h-pro-oh | |
| CHEBI:17203 | |
| OC(=O)C1CCCN1 |
Specifications
| ∽225°C (decomposition) | |
| C5H9NO2 | |
| 80810 | |
| Soluble in water and ethanol. Insoluble in ether,butanol and isopropanol. | |
| OC(=O)C1CCCN1 | |
| 115.13 | |
| CHEBI:17203 | |
| 1.36 | |
| L-Proline |
| 147-85-3 | |
| MFCD00064318 | |
| l-proline, proline, l---proline, s-pyrrolidine-2-carboxylic acid, 2-pyrrolidinecarboxylic acid, --proline, --s-proline, 2s-pyrrolidine-2-carboxylic acid, prolinum, h-pro-oh | |
| ONIBWKKTOPOVIA-UHFFFAOYNA-N | |
| (2S)-pyrrolidine-2-carboxylic acid | |
| 145742 | |
| 115.13 | |
| Hygroscopic |
Safety and Handling
missing translation for 'einecsNumber' : 205-702-2
missing translation for 'rtecsNumber' : TW3584000
missing translation for 'tsca' : Yes
Recommended Storage : Ambient temperatures
RUO – Research Use Only