5-Amino-1H-tetrazole potassium salt

Base Information

• Chemical Name: 5-Amino-1H-tetrazole potassium salt
• CAS No.: 136369-04-5
• Deprecated CAS: 1314913-67-1
• Molecular Formula: CH₂N₅*K
• Molecular Weight: 123.159
• European Community (EC) Number: 681-644-5
• DSSTox Substance ID: DTXSID601019341
• Mol file: 136369-04-5.mol

Synonyms:5-AMINO-1H-TETRAZOLE POTASSIUM SALT;136369-04-5;potassium;1,2,3-triaza-4-azanidacyclopenta-2,5-dien-5-amine;MFCD04038086;5-Aminotetrazole potassium salt;Potassium 5-aminotetrazol-1-ide;DTXSID601019341;AKOS006242580;5-Amino-1(H)-tetrazole potassium salt

Chemical Property of 5-Amino-1H-tetrazole potassium salt

Chemical Property:

• Vapor Pressure: 0Pa at 20℃
• PSA: 69.62000
• Density: 1.837 at 19.5℃
• LogP: -0.85110
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 0
• Exact Mass: 122.99472657
• Heavy Atom Count: 7
• Complexity: 47.3

Purity/Quality:

99.9% ^*data from raw suppliers

5-Amino-1H-tetrazolePotassiumSalt ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xn
• Hazard Codes: Xn
• Statements: 20/21/22-36/37/38
• Safety Statements: 26-36

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1(=NN=N[N-]1)N.[K+]
• Uses: 5-Amino-1H-tetrazole potassium salt is a useful intermediate in the synthesis of alkylated aminotetrazoles and their derivatives and can also be used as coloring agents in modern pyrotechnics, due to their high nitrogen content.

Technology Process of 5-Amino-1H-tetrazole potassium salt

There total 2 articles about 5-Amino-1H-tetrazole potassium salt which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 92.0%

5-aminotetrazole (4418-61-5) → 5-aminotetrazole potassium salt (136369-04-5)

Guidance literature:

With potassium hydroxide; In water; at 50 ℃;

DOI:10.1002/zaac.200900521

Reference yield: 78.0%

5-amino-2H-tetrazole (4418-61-5) → 5-aminotetrazole potassium salt (136369-04-5)

Guidance literature:

With potassium hydroxide; In water; Reflux;

DOI:10.1002/ejoc.200901175

Reference yield: 76.0%

salicylaldehyde (90-02-8) + 5-aminotetrazole potassium salt (136369-04-5) → potassium N-salicylidene 5-aminotetrazolate

Guidance literature:

In methanol; Reflux;

DOI:10.1002/ejoc.200901175

upstream raw materials:

5-aminotetrazole

5-amino-2H-tetrazole

Downstream raw materials:

1,5-diaminotetrazole

2,5-diaminotetrazole

Refernces

• 1、 Robert, Francois,Naik, Anil D.,Hidara, Florence,Tinant, Bernard,Robiette, Raphael,Wouters, Johan,Garcia, Yann. "Engineering solid-state molecular switches: N-salicylidene N-heterocycle derivatives". experimental part. p. 621 - 637. Retrieved 2010/03/26.