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2-Amino-2-methyl-1,3-propanediol (CAS 115-69-5)

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Alternate Names:
Ammediol
Application:
2-Amino-2-methyl-1,3-propanediol is a buffer and spacer in isotachophoresis of proteins
CAS Number:
115-69-5
Purity:
≥99%
Molecular Weight:
105.14
Molecular Formula:
C4H11NO2
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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2-Amino-2-methyl-1,3-propanediol is a multifunctional organic compound employed extensively across a range of scientific disciplines, primarily due to its unique chemical structure featuring both amino and hydroxyl groups. This configuration allows it to act as an effective buffer and intermediate in various chemical syntheses. In research, it is particularly valued for its role in the synthesis of pharmaceuticals, polymers, and surfactants, where its ability to introduce hydrophilic groups is critical. Its buffering capacity is utilized in biochemical studies to maintain pH stability in experimental assays, crucial for accurate enzymatic and protein interaction studies. Additionally, this compound serves as a building block in the production of corrosion inhibitors, which are essential in materials science for enhancing the durability and lifespan of metals under harsh conditions. In polymer chemistry, 2-amino-2-methyl-1,3-propanediol is used to modify polymer structures, thereby improving their hydrophilicity and biocompatibility, which is particularly useful in the development of hydrogels and other polymer-based materials used in research settings. This versatility makes it a vital tool in advancing the understanding of both organic synthesis and material properties, fostering significant contributions to fundamental research.


2-Amino-2-methyl-1,3-propanediol (CAS 115-69-5) References

  1. Preparation and characterisation of a range of diclofenac salts.  |  O'Connor, KM. and Corrigan, OI. 2001. Int J Pharm. 226: 163-79. PMID: 11532579
  2. Dirhodium(II)-catalyzed C-H amination reaction of (S)-3-(tert-butyldimethylsilyloxy)-2-methylpropyl carbamate: a facile preparation of optically active monoprotected 2-amino-2-methyl-1,3-propanediol.  |  Yakura, T., et al. 2007. Chem Pharm Bull (Tokyo). 55: 1385-9. PMID: 17827768
  3. DFT simulations and vibrational spectra of 2-amino-2-methyl-1,3-propanediol.  |  Renuga Devi, TS., et al. 2014. Spectrochim Acta A Mol Biomol Spectrosc. 133: 214-22. PMID: 24945862
  4. A [Ce21] keplerate.  |  Canaj, AB., et al. 2017. Dalton Trans. 46: 7677-7680. PMID: 28590003
  5. Inorganic Approach to Stabilizing Nanoscale Toroidicity in a Tetraicosanuclear Fe18Dy6 Single Molecule Magnet.  |  Kaemmerer, H., et al. 2020. J Am Chem Soc. 142: 14838-14842. PMID: 32786752
  6. The Influence of Selected Factors on the Aqueous Cryptotanshinone Solubility.  |  Kobryń, J., et al. 2021. Pharmaceutics. 13: PMID: 34209049
  7. Chemotactic responses of Brugia pahangi infective third-stage larvae to tris(hydroxymethyl)aminomethane-related compounds and amino acids.  |  Mitsui, Y., et al. 2021. J Helminthol. 95: e72. PMID: 34879884
  8. CO2 Capture and Release in Amine Solutions: To What Extent Can Molecular Simulations Help Understand the Trends?  |  Ma, C., et al. 2023. Molecules. 28: PMID: 37764223
  9. Taming heat with tiny pressure.  |  Zhang, K., et al. 2024. Innovation (Camb). 5: 100577. PMID: 38379786

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2-Amino-2-methyl-1,3-propanediol, 25 g

sc-256057
25 g
$49.00