Molecular structure of N-Isopropyl-N-methyl-tert-butylamine, CAS Number: 85523-00-8
N-Isopropyl-N-methyl-tert-butylamine (CAS 85523-00-8)
CAS Number:
85523-00-8
Purity:
≥98%
Molecular Weight:
129.24
Molecular Formula:
(CH3)3CN(CH3)CH(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
N-Isopropyl-N-methyl-tert-butylamine is an organic compound falling within the amine class. It plays a significant role as a reagent in the synthesis of diverse compounds. Additionally, it′s considered a weak base and has the capability to create complexes with metal ions.
N-Isopropyl-N-methyl-tert-butylamine (CAS 85523-00-8) References
- Asymmetric synthesis of primary amines via the spiroborate-catalyzed borane reduction of oxime ethers. | Huang, X., et al. 2007. Org Lett. 9: 1793-5. PMID: 17397177
- Towards a second generation of ionic liquid matrices (ILMs) for MALDI-MS of peptides, proteins, and carbohydrates. | Crank, JA. and Armstrong, DW. 2009. J Am Soc Mass Spectrom. 20: 1790-800. PMID: 19665903
- Recent advances in the synthesis of ammonium-based rotaxanes. | Thibeault, D. and Morin, JF. 2010. Molecules. 15: 3709-30. PMID: 20657509
- Retention Index Prediction Using Quantitative Structure-Retention Relationships for Improving Structure Identification in Nontargeted Metabolomics. | Wen, Y., et al. 2018. Anal Chem. 90: 9434-9440. PMID: 29952550
- Structure-Activity Relationship of para-Carborane Selective Estrogen Receptor β Agonists. | Sedlák, D., et al. 2021. J Med Chem. 64: 9330-9353. PMID: 34181409
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| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
N-Isopropyl-N-methyl-tert-butylamine, 5 ml | sc-236052 | 5 ml | $56.00 |