BICINE, 99%
Thermo Scientific Chemicals

BICINE, 99%

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1000 g
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Catalog number A14957.0B
also known as A14957-0B
Price (USD)/ Each
393.65
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437.00 
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Quantity:
1000 g
Request bulk or custom format
Price (USD)/ Each
393.65
Online exclusive
437.00 
Save 43.35 (10%)
Add to cart
BICINE, 99%
Catalog numberA14957.0B
Price (USD)/ Each
393.65
Online exclusive
437.00 
Save 43.35 (10%)
-
Add to cart
Chemical Identifiers
CAS150-25-4
IUPAC Namesodium 2-[bis(2-hydroxyethyl)amino]acetate
Molecular FormulaC6H12NNaO4
InChI KeyMFBDBXAVPLFMNJ-UHFFFAOYSA-M
SMILES[Na+].OCCN(CCO)CC([O-])=O
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SpecificationsSpecification SheetSpecification Sheet
FormCrystalline powder
Assay (Non-aqueous acid-base Titration)≥98.5 to ≤101.5%
Identification (FTIR)Conforms
Appearance (Color)White
Bicine is widely utilized as a buffering agent for low temperature work. It is used in kinetic study of a quaternary transition-state analogue complex of creatine kinase reaction. It is employed in the thin layer ion exchange chromatography method for protein resolution. It is employed in serum guanase determination by the preparation of stable substrate solution.

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
Bicine is widely utilized as a buffering agent for low temperature work. It is used in kinetic study of a quaternary transition-state analogue complex of creatine kinase reaction. It is employed in the thin layer ion exchange chromatography method for protein resolution. It is employed in serum guanase determination by the preparation of stable substrate solution.

Solubility
Soluble in water.

Notes
Store in cool place. Incompatible with strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Biological buffer, pK a = 8.35 at 20 ° : Biochemistry, 5, 467 (1966).
  2. Cowan, E. A.; Oldham, C. D.; May, S. W. Identification of a thioselenurane intermediate in the reaction between phenylaminoalkyl selenoxides and glutathione. Arch. Biochem. Biophys. 2011, 506 (2), 201-207.
  3. Tainaka, K.; Kubota, S. I.; Suyama, T. Q.; Susaki, E. A.; Perrin, D.; Tadenuma, M. U.; Ukai, H.; Ueda, H. R. Whole-Body Imaging with Single-Cell Resolution by Tissue Decolorization. Cell 2014, 159 (4), 911-924.