AI07065
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
5g | 96% | in stock | $10.00 | $7.00 | - + | |
10g | 96% | in stock | $19.00 | $13.00 | - + | |
25g | 96% | in stock | $29.00 | $20.00 | - + | |
100g | 96% | in stock | $92.00 | $65.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AI07065 |
Chemical Name: | DL-Ornithine HCl |
CAS Number: | 1069-31-4 |
Molecular Formula: | C5H13ClN2O2 |
Molecular Weight: | 168.62192000000002 |
MDL Number: | MFCD11544197 |
SMILES: | NC(C(=O)O)CCCN.Cl |
Complexity: | 95 |
Covalently-Bonded Unit Count: | 2 |
Heavy Atom Count: | 10 |
Hydrogen Bond Acceptor Count: | 4 |
Hydrogen Bond Donor Count: | 4 |
Rotatable Bond Count: | 4 |
Undefined Atom Stereocenter Count: | 1 |
DL-Ornithine hydrochloride, a key intermediate in various chemical syntheses, serves as a versatile building block in organic chemistry. Its unique structure and functional groups make it a valuable tool for the preparation of diverse compounds and materials.In chemical synthesis, DL-Ornithine hydrochloride is commonly utilized in the creation of pharmaceuticals, agrochemicals, and specialty chemicals. Its involvement in the synthesis of amino acids, peptides, and chiral compounds underscores its significance in the field. By participating in various reactions such as condensation, esterification, and hydrolysis, DL-Ornithine hydrochloride enables the formation of complex structures with high stereochemical purity.Moreover, DL-Ornithine hydrochloride plays a crucial role in the production of bioactive molecules, enzyme inhibitors, and drug candidates. Its compatibility with a wide range of reagents and reaction conditions makes it a preferred choice for chemists seeking efficient routes to target molecules. Whether used as a precursor, reagent, or chiral auxiliary, DL-Ornithine hydrochloride offers chemists a powerful tool to advance their synthetic endeavors and achieve desired chemical transformations.