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Thermo Scientific Chemicals
L-Lysine monohydrate, 97%
CAS: 39665-12-8 | C6H16N2O3 | 164.21 g/mol
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化學識別
CAS39665-12-8
IUPAC Name(2S)-2,6-diaminohexanoic acid hydrate
Molecular FormulaC6H16N2O3
InChI KeyHZRUTVAFDWTKGD-XZNNNFJINA-N
SMILESO.NCCCC[C@H](N)C(O)=O
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規格
規格表
規格表Assay (Non-aqueous acid-base Titration)≥96.0 to ≤104.0% (UK-sourced material)
Assay from Supplier's CofA≥96.0% (US-sourced material)
Water Content (Karl Fischer Titration)5.8-15.6% (0.5-1.5 waters, UK-sourced material)
Optical Rotation22.6 ± 0.5° (C = 2 in 6M HCl, UK-sourced material)
Appearance (Color)White to cream to pale yellow
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L-Lysine is an essential proteinogenic alfa amino acid used in various applications such as non-animal sourced supplement in cell culture media. It acts as a substrate of enzymes like L-lysine oxidase as well as a component of poly-lysine polymers. It is also involved in the studies of glycation mechanism.
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
L-Lysine is an essential proteinogenic alfa amino acid used in various applications such as non-animal sourced supplement in cell culture media. It acts as a substrate of enzymes like L-lysine oxidase as well as a component of poly-lysine polymers. It is also involved in the studies of glycation mechanism.
Solubility
Soluble in water and hydrochloric acid.
Notes
Hygroscopic. Air sensitive. Incompatible with strong oxidizing agents.
L-Lysine is an essential proteinogenic alfa amino acid used in various applications such as non-animal sourced supplement in cell culture media. It acts as a substrate of enzymes like L-lysine oxidase as well as a component of poly-lysine polymers. It is also involved in the studies of glycation mechanism.
Solubility
Soluble in water and hydrochloric acid.
Notes
Hygroscopic. Air sensitive. Incompatible with strong oxidizing agents.
RUO – Research Use Only
General References:
- Bashir, M. S.; Ali, S.; Shahzadi, S.; Shahid, M. Synthesis, characterization and biological activities of organotin(IV) complexes with l-lysine monohydrate. Russ. J. Gen. Chem. 2015, 85 (6), 1532-1537.
- Zuravka, I.; Roesmann, R.; Sosic, A.; Göttlich, R.; Gatto, B. Bis-3-chloropiperidines containing bridging lysine linkers: Influence of side chain structure on DNA alkylating activity. Bioorg. Med. Chem. 2015, 23 (6), 1241-1250.