L-Proline hydrochloride
- Name: L-Proline hydrochloride
- CAS: 7776-34-3
- Purity: 99%
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Description
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What is the L-Proline hydrochloride ?
L-Proline hydrochloride is , while it's Molecular Formula is C5H9NO2. HCl. Used in Pharmaceutical Industry:
L-Proline hydrochloride is used as a pharmaceutical ingredient for the production of drugs, contributing to the development of medications that target various health conditions.
Used in Cell Culture Media:
L-Proline hydrochloride is used as a supplement in cell culture media to support cell growth and maintenance, ensuring optimal conditions for research and development in biological and medical studies.
Used in Organic Synthesis:
L-Proline hydrochloride is used as a chiral auxiliary in organic chemistry reactions, facilitating the synthesis of enantiomerically pure compounds, which are crucial for the development of effective and safe pharmaceuticals.
Used in Peptide Synthesis:
L-Proline hydrochloride is used in the synthesis of peptides, playing a vital role in the creation of bioactive molecules with potential applications in medicine and biotechnology.What is the CAS number for L-Proline hydrochloride ?
The CAS number of L-Proline hydrochloride is 7776-34-3.
More information of L-Proline hydrochloride 7776-34-3 are:
Synonyms
L-Proline,hydrochloride (9CI);Proline, hydrochloride, L- (8CI);L-Prolinemonohydrochloride;Proline hydrochloride; CAS?Number
7776-34-3 Molecular Formula
C5H9NO2. HCl Molecular Weight
151.593 Melting Point
155 °C Boiling Point
252.2 °C at 760 mmHg Flash Point
106.3 °C PSA
49.33000 LogP
0.95380 What is L-Proline hydrochloride (7776-34-3) used for?
L-Proline hydrochloride is a chemical compound that is the hydrochloride salt form of L-proline, a non-essential amino acid. It is an important building block for many proteins and enzymes in the body, playing a key role in collagen formation, wound healing, and maintaining healthy skin and connective tissues. Additionally, it is used in the synthesis of peptides and as a chiral auxiliary in organic chemistry reactions.
InChI:InChI=1/C5H9NO2.ClH/c7-5(8)4-2-1-3-6-4;/h4,6H,1-3H2,(H,7,8);1H/t4-;/m0./s1
Articles related to L-Proline hydrochloride:
Article
Source
Diastereoselective hydrogenation of pyrazine derivatives: An alternative method of preparing piperazine-(2S)-carboxylic acid
Kukula, Pavel,Prins, Roel
, p. 404 - 411 (2002)
Room temperature depolymerization of lignin using a protic and metal based ionic liquid system: an efficient method of catalytic conversion and value addition
Mehta, Mohit J.,Kulshrestha, Akshay,Sharma, Shweta,Kumar, Arvind
, p. 1240 - 1247 (2021/02/26)
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