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2,6-Diaminopimelic acid, 96%, Thermo Scientific Chemicals
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Catalog number B22391.06
Price (USD)/ Each
156.65
Online exclusive
174.00 Save 17.35 (10%)
-
Quantity:
5 g
Price (USD)/ Each
156.65
Online exclusive
174.00 Save 17.35 (10%)
2,6-Diaminopimelic acid, 96%, Thermo Scientific Chemicals
Catalog numberB22391.06
Price (USD)/ Each
156.65
Online exclusive
174.00 Save 17.35 (10%)
-
Chemical Identifiers
CAS583-93-7
IUPAC Name(2R,6S)-2,6-diazaniumylheptanedioate
Molecular FormulaC7H14N2O4
InChI KeyGMKMEZVLHJARHF-SYDPRGILSA-N
SMILES[NH3+][C@@H](CCC[C@@H]([NH3+])C([O-])=O)C([O-])=O
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Specifications
Specification Sheet
Specification SheetAppearance (Color)White to cream to pale brown
FormPowder and/or chunks
Assay (Non-aqueous acid-base Titration)≥95.0 to ≤105.0%
Identification (FTIR)Conforms
2,6-Diaminopimelic acid is used as a constituent of proteoglycans. It is used as a component of bacterial cell wall.
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
2,6-Diaminopimelic acid is used as a constituent of proteoglycans. It is used as a component of bacterial cell wall.
Solubility
Soluble in water, diluted acids and alkali.
Notes
Incompatible with strong oxidizing agents.
2,6-Diaminopimelic acid is used as a constituent of proteoglycans. It is used as a component of bacterial cell wall.
Solubility
Soluble in water, diluted acids and alkali.
Notes
Incompatible with strong oxidizing agents.
RUO – Research Use Only
General References:
- Hanson, R. L.; Johnston, R. M.; Goldberg, S. L.; Parker, W. L.; Goswami, A.Enzymatic Preparation of an R-Amino Acid Intermediate for a γ-Secretase Inhibitor. Org. Process Res. Dev. 2013, 17 (4), 693-700.
- Wyckoff, T. J.; Taylor, J. A.; Salama, N. R. Beyond growth: novel functions for bacterial cell wall hydrolases. Trends Microbiol. 2012, 20 (11), 540-547.
- Stegmann, E.; Frasch, H- J.; Kilian, R.; Pozzi, R. Self-resistance mechanisms of actinomycetes producing lipid II-targeting antibiotics. Int. J. Med. Microbiol. 2015, 305 (2), 190-195.