Tetrapropylammonium bromide

• CAS: 1941-30-6
• Catalog Number: ACM1941306-1
• Category: Other Products
• Molecular Weight: 266.27
• Molecular Formula: C12H28BrN
• Synonyms: Tetrapropylam
• IUPAC Name: Tetrapropylazanium;bromide
• Canonical SMILES: CCC[N+](CCC)(CCC)CCC.[Br-]
• InChI: InChI=1S/C12H28N.BrH/c1-5-9-13(10-6-2,11-7-3)12-8-4;/h5-12H2,1-4H3;1H/q+1;/p-1
• InChI Key: BGQMOFGZRJUORO-UHFFFAOYSA-M
• Melting Point: 266-272 °C
• Solubility: Soluble in water
• Appearance: Colorless or white crystal
• Storage: Store below +30 °C
• Complexity: 80.2
• Covalently-Bonded Unit Count: 2
• EC Number: 217-727-6
• Exact Mass: 265.14051
• H-Bond Acceptor: 1
• Heavy Atom Count: 14
• Monoisotopic Mass: 265.14051
• Physical Description: TETRAPROPYLAMMONIUM BROMIDE is a white to off-white crystalline solid. (NTP, 1992)
• Physical State: Colorless to white crystal
• Refractive Index: 1.526
• Rotatable Bond Count: 8
• Topological Polar Surface Area: 0 Ų
• UNII: 220T63791N

Synthetic Use

Upstream Synthesis Route 1

• 102-69-2
• 106-94-5

• 1941-30-6

Reference: [1] Journal of pharmaceutical sciences, 1966, vol. 55, # 4, p. 414 - 417
[2] Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases, 1989, vol. 85, # 9, p. 2669 - 2674
[3] Dalton Transactions, 2015, vol. 44, # 38, p. 16680 - 16683
[4] Australian Journal of Chemistry, 2018, vol. 71, # 6, p. 435 - 441

Upstream Synthesis Route 2

• 106-94-5

• 1941-30-6

Reference: [1] Patent: US4931593, 1990, A,

Upstream Synthesis Route 3

• 102-69-2
• 106-94-5

• 1941-30-6

Reference: [1]Journal of Pharmaceutical Sciences,1966,vol. 55,p. 414 - 417
[2]Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases,1989,vol. 85,p. 2669 - 2674
[3]Dalton Transactions,2015,vol. 44,p. 16680 - 16683
[4]Australian Journal of Chemistry,2018,vol. 71,p. 435 - 441

Downstream Synthesis Route 1

• 1941-30-6
• 110-83-8

• 5401-62-7
• 1521-51-3

Reference: [1] Journal of the American Chemical Society, 2011, vol. 133, # 6, p. 1832 - 1848

* For details of the synthesis route, please refer to the original source to ensure accuracy.