Tri-n-hexylamine, 96%
Tri-n-hexylamine, 96%
Tri-n-hexylamine, 96%
Tri-n-hexylamine, 96%
Thermo Scientific Chemicals

Tri-n-hexylamine, 96%

CAS: 102-86-3 | C18H39N | 269.517 g/mol
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250 g
Catalog number B23716.30
also known as B23716-30
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Quantity:
250 g
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Price (USD)
286.65
Online Exclusive
318.00
Save 31.35 (10%)
Each
Add to cart
Chemical Identifiers
CAS102-86-3
SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear colorless to pale yellow
FormLiquid
Assay (GC)≥95.0%
Refractive Index1.4390-1.4440 @20?C
Tri-n-hexylamine is used as an extractant during isolation and purification of succinic acid from an escherichia coli fermentation broth in pharmaceutical industry. It is also used as an internal standard in screening of human hair specimens for designer drugs by ion mobility spectrometry. Further, it is involved in the synthesis of zinc oxide nanorods. In addition to this, it is used in the preparation of infrared luminescence nanohybrid films.

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
Tri-n-hexylamine is used as an extractant during isolation and purification of succinic acid from an escherichia coli fermentation broth in pharmaceutical industry. It is also used as an internal standard in screening of human hair specimens for designer drugs by ion mobility spectrometry. Further, it is involved in the synthesis of zinc oxide nanorods. In addition to this, it is used in the preparation of infrared luminescence nanohybrid films.

Solubility
Slightly miscible with water.

Notes
Incompatible with strong oxidizing agents, acids, acid chloridres, acid anhydrides and chloroformates.
RUO – Research Use Only

General References:

  1. Ansari, S. A.; Mohapatra, P. K.; Mazan, V.; Billard, I. Extraction of actinides by tertiary amines in room temperature ionic liquids: evidence for anion exchange as a major process at high acidity and impact of acid nature. RSC Adv. 2015, 5 (45), 35821-35829.
  2. Ma, D.; Li, B.; Liu, K.; Zhang, X.; Zou, W.; Yang, Y.; Li, G.; Shi, Z.; Feng, S. Bifunctional MOF heterogeneous catalysts based on the synergy of dual functional sites for efficient conversion of CO2 under mild and co-catalyst free conditions. J. Mater. Chem. A 2015, 3 (46), 23136-23142.