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DL-Ornithine monohydrochloride, 99%, Thermo Scientific Chemicals
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Catalog number A18173.18
also known as A18173-18
Price (USD)/ Each
155.00
-
Quantity:
50 g
Price (USD)/ Each
155.00
DL-Ornithine monohydrochloride, 99%, Thermo Scientific Chemicals
Catalog numberA18173.18
Price (USD)/ Each
155.00
-
Chemical Identifiers
CAS1069-31-4
IUPAC Namehydrogen 2,5-diaminopentanoic acid chloride
Molecular FormulaC5H13ClN2O2
InChI KeyGGTYBZJRPHEQDG-UHFFFAOYNA-N
SMILES[H+].[Cl-].NCCCC(N)C(O)=O
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Specifications
Specification Sheet
Specification SheetAppearance (Color)White
FormCrystals or powder or crystalline powder
Assay (Titration ex Chloride)≥98.5 to ≤101.5%
Erythro-3-hydroxy-DL-ornithine monohydrochloride is used as a reagent to synthesize DL-Capreomycidine, a guanidine (HCl)-containing amino acid that is a component of antituberculous peptides.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Erythro-3-hydroxy-DL-ornithine monohydrochloride is used as a reagent to synthesize DL-Capreomycidine, a guanidine (HCl)-containing amino acid that is a component of antituberculous peptides.
Solubility
Soluble in water.
Notes
Store away from oxidizing agents. Keep the container tightly closed and place it in a cool, dry and well ventilated condition.
Erythro-3-hydroxy-DL-ornithine monohydrochloride is used as a reagent to synthesize DL-Capreomycidine, a guanidine (HCl)-containing amino acid that is a component of antituberculous peptides.
Solubility
Soluble in water.
Notes
Store away from oxidizing agents. Keep the container tightly closed and place it in a cool, dry and well ventilated condition.
RUO – Research Use Only
General References:
- Manami Oya.; Tetsuya Kitaguchi.; Ramona Pais.; Frank Reimann.; Fiona Gribble.; Takashi Tsuboi. The G protein-coupled receptor family C group 6 subtype A (GPRC6A) receptor is involved in amino acid-induced glucagon-like peptide-1 secretion from GLUTag cells.J Biol Chem.2013,288(7), 4513-4521.
- DeMong, D. & Williams, R. The asymmetric synthesis of (2S,3R)-capreomycidine.Tetrahedron Lett.2001,42(21), 3529-3532.