| Bioactivity | L-Hydroxyproline, one of the hydroxyproline (Hyp) isomers, is a useful chiral building block in the production of many pharmaceuticals. | ||||||||||||
| Invitro | L-Hydroxyproline (Trans-4-hydroxy-L-proline;Trans-Hyp) has been widely used in medicine, biochemistry, food, cosmetic and other aspects of industry. Additionally, L-Hydroxyproline has also been found in the composition of some secondary metabolites such as actinomycins and echinocandins. L-Hydroxyproline is manufactured industrially most by acid hydrolysis of mammalian collagen because of its rich amount in the collagen[1]. | ||||||||||||
| Name | L-Hydroxyproline,BioReagent, suitable for cell culture | ||||||||||||
| CAS | 51-35-4 | ||||||||||||
| Formula | C5H9NO3 | ||||||||||||
| Molar Mass | 131.13 | ||||||||||||
| Transport | Room temperature in continental US; may vary elsewhere. | ||||||||||||
| Storage |
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L-Hydroxyproline,BioReagent, suitable for cell culture
CAS: 51-35-4 F: C5H9NO3 W: 131.13
L-Hydroxyproline, one of the hydroxyproline (Hyp) isomers, is a useful chiral building block in the production of many p
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