Date published: 2025-9-16

1-800-457-3801

SCBT Portrait Logo
Seach Input

Tetraheptylammonium chloride (CAS 10247-90-2)

0.0(0)
Write a reviewAsk a question

Application:
Tetraheptylammonium chloride is an ionic compound used in specialty chemical synthesis
CAS Number:
10247-90-2
Molecular Weight:
446.24
Molecular Formula:
C28H60ClN
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

Tetraheptylammonium chloride is an ionic compound used in specialty chemical synthesis. Tetraheptylammonium chloride is a quaternary ammonium compound employed as a phase transfer catalyst in organic synthesis. It assists in transferring ions or molecules between different immiscible phases. With its unique structure, it enhances various chemical reactions and improves yields. Tetraheptylammonium chloride finds applications in nucleophilic substitutions, oxidations, and polymerizations, aiding in reaction rates and solubility.


Tetraheptylammonium chloride (CAS 10247-90-2) References

  1. Efficient extraction of bile acid conjugates with tetraheptylammonium chloride, a liquid ion exchanger.  |  Hofmann, AF. 1967. J Lipid Res. 8: 55-8. PMID: 14564706
  2. Selectivity control in synergistic liquid-liquid anion exchange of univalent anions via structure-specific cooperativity between quaternary ammonium cations and anion receptors.  |  Borman, CJ., et al. 2012. Anal Chem. 84: 8214-21. PMID: 22931168
  3. Construction of a p-nitrophenolate-sensitive membrane electrode and its application to an enzyme assay.  |  Katsu, T., et al. 1987. Chem Pharm Bull (Tokyo). 35: 3922-4. PMID: 3435986
  4. Metabolic disposition of cephalothin and deacetylcephalothin in children and adults: comparison of high-performance liquid chromatographic and microbial assay procedures.  |  Rolewicz, TF., et al. 1977. Clin Pharmacol Ther. 22: 928-35. PMID: 411623
  5. Ion-pair extraction and high-speed liquid chromatography of cephalothin and deacetylcephalothin in human serum and urine.  |  Cooper, MJ., et al. 1973. Drug Metab Dispos. 1: 659-62. PMID: 4149703
  6. Liquid ion exchangers for chromatography of steroidal glucosiduronic acids and other polar compounds.  |  Mattox, VR., et al. 1972. J Chromatogr. 66: 337-46. PMID: 5019968
  7. Extraction of steroidal glucosideronic acids from aqueous solutions by anionic liquid ion-exchangers.  |  Mattox, VR., et al. 1972. Biochem J. 126: 533-43. PMID: 5075264
  8. Recovery of steroidal glucosiduronic acids from organic solvents containing anionic liquid ion-exchangers.  |  Mattox, VR., et al. 1972. Biochem J. 126: 545-52. PMID: 5075265
  9. Use of anionic liquid ion exchangers in the chromatography of steroidal glucosiduronic acids.  |  Mattox, VR., et al. 1970. J Chromatogr. 48: 123-4. PMID: 5459019
  10. The isolation and further characterization of the bilirubin tetrapyrroles in bile-containing human duodenal juice and dog gall-bladder bile.  |  Gordon, ER., et al. 1977. Biochem J. 167: 1-8. PMID: 588243
  11. Mechanism and subcellular site of bilirubin diglucuronide formation in rat liver.  |  Gordon, ER., et al. 1984. J Biol Chem. 259: 5500-6. PMID: 6715357
  12. Extraction of platinum and palladium with bis (2, 4, 4-trimethylpentyl)-phosphinodithioic acid.  |  Saito, K., & Freiser, H. (1989). Analytical sciences,. 5(5),: 583-586.
  13. Hydrophobic deep eutectic solvents as water-immiscible extractants.  |  van Osch, D. J., Zubeir, L. F., van den Bruinhorst, A., Rocha, M. A., & Kroon, M. C. (. 2015). Green Chemistry,. 17(9),: 4518-4521.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Tetraheptylammonium chloride, 1 g

sc-229415
1 g
$87.00

Tetraheptylammonium chloride, 5 g

sc-229415A
5 g
$413.00