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L-HYDROXYPROLINE | ||
PRODUCT IDENTIFICATION |
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CAS NO. | 51-35-4 |
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EINECS NO. | 200-091-9 | |
FORMULA | C5H9NO3 | |
MOL WT. | 131.13 | |
H.S. CODE |
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TOXICITY |
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SYNONYMS | 4-hydroxy-L-proline; 4-hydroxyproline; | |
(2S,4S)-4-hydroxyproline; (4S)-4-hydroxy-L-proline; Hydroxyproline; L-4-hydroxyproline; trans-4-Hydroxy-L-Proline; trans-4-hydroxyproline; L-4-hidroxiprolina; (2S,4R)-(-)- 4-hydroxy-2-pyrrolidinecarboxylic acid; (2S,4R)-4-Hydroxypyrrolidine- 2-carboxylic acid; | ||
SMILES |
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CLASSIFICATION |
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PHYSICAL AND CHEMICAL PROPERTIES |
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PHYSICAL STATE | white crystalline powder | |
MELTING POINT | 274 - 275 C 9Decomposes) | |
BOILING POINT | ||
SPECIFIC GRAVITY | ||
SOLUBILITY IN WATER | 355 g/l at 20 C | |
pH | ||
VAPOR DENSITY | ||
AUTOIGNITION |
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NFPA RATINGS |
Health: 1 Flammability: 0 Reactivity: 0 | |
REFRACTIVE INDEX |
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FLASH POINT |
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STABILITY | Stable under ordinary conditions. | |
GENERAL DESCRIPTION AND APPLICATIONS |
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Hydroxyproline, a hydroxylated form of the imino acid proline, is a major component of collagen which is located in the extracellular matrix of connective tissues to contribute to tissue integrity and mechanical properties of ligament strength and skin flexibility. The major form is 4-hydroxyproline, but 3-hydroxy form is also present. The human body makes proline which is converted to hydroxyproline in the presence of vitamin C. L-Hydroxyproline can be used in the synthesis of mycology medicals (anti-fungals) and chiral ligands (enantioselective ethylation of aldehydes) | ||
SALES SPECIFICATION | ||
APPEARANCE |
white crystalline powder | |
ASSAY |
97.0 - 101.0% |
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SPECIFIC ROTATION |
-74.0° ~ -77.0° |
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Cl |
0.02% max |
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NH4 |
0.02% max |
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SO4 |
0.02% max |
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Fe |
10ppm mqx |
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HEAVY METALS |
10ppm max |
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As |
1ppm max |
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LOSS ON DRYING |
0.2% max |
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RESIDUE ON IGNITION |
0.1% max |
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pH |
5.0 - 6.5 |
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TRANSPORTATION | ||
PACKING | | |
HAZARD CLASS | Not regulated | |
UN NO. | ||
OTHER INFORMATION | ||
Hazard Symbols: , Risk Phrases: , Safety Phrases: 24/25 | ||
PRICE INFORMATION |
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