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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 344622Generated: October 29, 2026

593-85-1 → HCID 131717018, compound

https://huagongshe.com/reaction/344622

Reaction equation

Participants

RoleNameHCIDCharge
Reactant593-85-1HCID 11789194—
ReactantHCID 178507071HCID 178507071—
SolventWaterHCID 962—
ProductHCID 131717018HCID 131717018—

Reaction Steps

The high nitrogen content solid is then added to form a uniform suspension. A catalyst such as dibutyltin dilaurate is also used. The solids ammonium 5-nitraminotetrazole and triaminoguanidinium 5-nitraminotetrazole, are synthesized by known methods. Aminoguanidinium 5,5'-bitetrazole is synthesized by dissolving 5,5'-bitetrazole (12.7g) and aminoguanidinium bicarbonate (12.5g) in boiling water (160 ml). The solution is filtered while hot and the filtrate rapidly chilled in an ice bath. The product is filtered off, washed twice with cold water and vacuum dried at 70° C., 25 mm to give a 91% (17.8g) yield of aminoguanidinium 5,5'-bitetrazole. The solid guanidinium 5,5'-bitetrazole is synthesized by adding a filtered solution of guanidinium bicarbonate (9.0g, 0.05 mole) in boiling water (75 ml) to a filtered boiling solution of 5,5'-bitetrazole (13.8g, 0.1 mole) in water (200 ml). The resulting solution is cooled rapidly in an ice-water bath. The white, crystalline product is removed by filtration, washed once with cold water and vacuum dried at 70° C., 25 mm to give a 95.6% (18.8g) yield of guanidinium 5,5'-bitetrazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05053086
Source datasetuspto-grants-1991_10
ORD IDord-f78ce770e53549a781cf9fcaba084ada
Source noteuspto-grants-1991_10