Date published: 2025-9-26

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Tripentylamine (CAS 621-77-2)

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Alternate Names:
Triamylamine, mixed isomers
CAS Number:
621-77-2
Purity:
≥97%
Molecular Weight:
227.43
Molecular Formula:
C15H33N
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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Tripentylamine functions as a tertiary amine in experimental applications. It acts as a base, readily accepting protons to form a positively charged ammonium ion. This allows it to participate in various reactions, including the formation of salts and the synthesis of organic compounds. At the molecular level, tripentylamine interacts with other molecules by donating its lone pair of electrons, facilitating the formation of new chemical bonds. This mechanism of action enables it to play a functional role in the modification of organic molecules and the production of specific chemical derivatives. In experimental applications, tripentylamine′s ability to act as a base and participate in chemical reactions may be useful for studying organic synthesis and chemical transformations. Its mechanism of action at the molecular level allows for the manipulation of chemical structures and the creation of novel compounds.


Tripentylamine (CAS 621-77-2) References

  1. Benzoxazine/Triphenylamine-Based Dendrimers Prepared through Facile One-Pot Mannich Condensations.  |  Lin, RC., et al. 2017. Macromol Rapid Commun. 38: PMID: 28671748
  2. A Spherically Shielded Triphenylamine and Its Persistent Radical Cation.  |  Schaub, TA., et al. 2020. Chemistry. 26: 3264-3269. PMID: 31970834
  3. Luminescent triphenylamine-based metal-organic frameworks: recent advances in nitroaromatics detection.  |  Shi, ZQ., et al. 2020. Dalton Trans. 49: 12929-12939. PMID: 32902551
  4. Novel Photoinitiators Based on Benzophenone-Triphenylamine Hybrid Structure for LED Photopolymerization.  |  Liu, S., et al. 2020. Macromol Rapid Commun. 41: e2000460. PMID: 32959447
  5. Theoretical Investigation on Photophysical Properties of Triphenylamine and Coumarin Dyes.  |  Li, X., et al. 2020. Materials (Basel). 13: PMID: 33137902
  6. Triphenylamine/4,4'-Dimethoxytriphenylamine-Functionalized Thieno[3,2-b]thiophene Fluorophores with a High Quantum Efficiency: Synthesis and Photophysical Properties.  |  Isci, R., et al. 2021. J Phys Chem B. 125: 13309-13319. PMID: 34807616
  7. Cucurbituril hosts as promoters of aggregation induced emission of triphenylamine derivatives.  |  Delgado-Pinar, E., et al. 2022. Phys Chem Chem Phys. 24: 2403-2411. PMID: 35019912
  8. Cellular Detection of a Mitochondria Targeted Brominated Vinyl Triphenylamine Optical Probe (TP-Br) by X-Ray Fluorescence Microscopy.  |  Nagarajan, S., et al. 2022. Chemistry. 28: e202104424. PMID: 35076130
  9. A π-extended triphenylamine based dopant-free hole-transporting material for perovskite solar cells via heteroatom substitution.  |  Hao, M., et al. 2022. Phys Chem Chem Phys. 24: 4635-4643. PMID: 35133365
  10. One-pot synthesis of conjugated triphenylamine macrocycles and their complexation with fullerenes.  |  Lu, YB., et al. 2021. RSC Adv. 11: 33431-33437. PMID: 35497513
  11. Triphenylamine, Carbazole or Tetraphenylethylene-Functionalized Benzothiadiazole Derivatives: Aggregation-Induced Emission (AIE), Solvatochromic and Different Mechanoresponsive Fluorescence Characteristics.  |  Yang, Y., et al. 2022. Molecules. 27: PMID: 35897916
  12. Synthesis of innovative triphenylamine-functionalized organic photosensitizers outperformed the benchmark dye N719 for high-efficiency dye-sensitized solar cells.  |  Badawy, SA., et al. 2022. Sci Rep. 12: 12885. PMID: 35902707
  13. Synthesis of Novel Triphenylamine-Based Organic Dyes with Dual Anchors for Efficient Dye-Sensitized Solar Cells.  |  Mahmoud, SE., et al. 2022. Nanoscale Res Lett. 17: 71. PMID: 35927533
  14. Spectroscopic and Physicochemical Investigations of Azomethines with Triphenylamine Core towards Optoelectronics.  |  Amin, MF., et al. 2022. Materials (Basel). 15: PMID: 36295266

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Tripentylamine, 25 ml

sc-237357
25 ml
$56.00

Tripentylamine, 250 ml

sc-237357A
250 ml
$153.00

Tripentylamine, 2 L

sc-237357B
2 L
$1132.00