Molecular structure of 3,5,N,N-Tetramethylaniline, CAS Number: 4913-13-7
3,5,N,N-Tetramethylaniline (CAS 4913-13-7)
Alternate Names:
5-(Dimethylamino)-m-xylene; N,N-Dimethyl-sym.-xylidene
Application:
3,5,N,N-Tetramethylaniline is a derivitized aniline
CAS Number:
4913-13-7
Purity:
≥98%
Molecular Weight:
149.23
Molecular Formula:
(CH3)2C6H3N(CH3)2
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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SDS & Certificate of Analysis
3,5,N,N-Tetramethylaniline is an aniline derivative, which functions as a catalyst in the formation of glycol methacrylate, an embedding medium. Studies indicate that 3,5,N,N-Tetramethylaniline can act as a quencher, rapidly binding to 1,8-Dihydroxyanthraquinone (DHAQ) (sc-223124). Anilines are aromatic amines, which are useful in a wide variety of reactions such as oxidations into azobenzenes, electrophilic substitutions, and acid base reactions. As a result of the amino group, this organic compound functions as a weak base, which can react with carboxylic acids, forming amides.
3,5,N,N-Tetramethylaniline (CAS 4913-13-7) References
- Generalization of ionic partition diagrams to lipophilic compounds and to biphasic systems with variable phase volume ratios. | Gobry, V., et al. 2001. J Am Chem Soc. 123: 10684-90. PMID: 11674000
- Reactivity of aromatic amines with triplet 1,8-dihydroxyanthraquinone: a laser flash photolysis study. | Pan, Y., et al. 2007. Spectrochim Acta A Mol Biomol Spectrosc. 66: 63-7. PMID: 16815083
- Metal-Specific Biomaterial Accumulation in Human Peri-Implant Bone and Bone Marrow. | Schoon, J., et al. 2020. Adv Sci (Weinh). 7: 2000412. PMID: 33101844
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| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
3,5,N,N-Tetramethylaniline, 25 g | sc-252066 | 25 g | $105.00 |