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Manufacturer supply top purity L-Proline 147-85-3 with ISO standards We supply high quality L-Proline (CAS 147-85-3), in stock, factory directly supply to clients, lower prices, more competitiveness.
L-Proline is White crystalline powder, while it's Molecular Formula is C5H9NO2. L-Proline is an amino acid and precursor (with vitamin C) for collagen, the building block of the structure of tendons, ligaments, arteries, veins and muscles. It is important in wound healing.
The CAS number of L-Proline is 147-85-3.
More information of L-Proline 147-85-3 are:
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Synonyms |
L-Prolin;(S)-Pyrrolidine-2-carboxylic acid;L-Pyrrolidine-2-carboxylic acid;(-)-Proline (S)-2-Carboxypyrrolidine;CCCu;2-Pyrralidinecarboxylic acid, (S)-;2-Pyrrolidinecarboxylic acid, (S)-;(-)-2-Pyrrolidinecarboxylic acid;L-(-)-Proline;PRO;(2S)-2,3,4,5-tetrahydropyrrole-2-carboxylate;(S)-Proline;(-)-(S)-Proline;H-Pro-OH~(S)-Pyrrolidine-2-carboxylic acid; |
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CAS Number |
147-85-3 |
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Molecular Formula |
C5H9NO2 |
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Molecular Weight |
115.132 |
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Density |
1.186 g/cm3 |
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Melting Point |
228 °C (dec.)(lit.) |
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Boiling Point |
252.2 °C at 760 mmHg |
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Flash Point |
106.3 °C |
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HS CODE |
2922.49 |
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PSA |
49.33000 |
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LogP |
0.15180 |
|
Pka |
1.95, 10.64(at 25℃) |
L-Proline is a non-essential amino acid that serves as a crucial building block for proteins. It is unique among the twenty DNA-encoded amino acids, as it has a secondary amino group alpha to the carboxyl group. L-Proline plays a significant role in the formation of collagen, which is vital for the proper functioning of joints, tendons, and heart muscles. It is also recognized for its osmoprotectant properties and is used in various applications across different industries.
InChI:InChI=1/C5H9NO2/c7-5(8)4-2-1-3-6-4/h4,6H,1-3H2,(H,7,8)/t4-/m1/s1
Articles related to L-Proline:
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Article |
Source |
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Optical resolution, characterization, and X-ray crystal structures of diastereomeric salts of chiral amino acids with (S)-(-)-1-phenylethanesulfonic acid |
Yoshioka,Ohtsuki,Da-Te,Okamura,Senuma , p. 3012 - 3020 (1994) |
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The relative catalytic efficiency of β-lactamase catalyzed acyl and phosphyl transfer |
Slater, Martin J.,Laws, Andrew P.,Page, Michael I. , p. 77 - 95 (2001) |
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