Beta-Alanine → HCID 86628860, compound

HRID 1846923Notes

Reaction equation

HRID 1846923 reaction equation
[N+:1]([O-:4])([OH:3])=[O:2].[NH2:5][CH2:6][CH2:7][C:8]([OH:10])=[O:9].[N+:11]([O-:14])([OH:13])=[O:12].[NH2:15][CH2:16][CH2:17][C:18]([OH:20])=[O:19]>O>[N+:1]([O-:4])([OH:3])=[O:2].[N+:11]([O-:14])([OH:13])=[O:12].[NH2:5][CH2:6][CH2:7][C:8]([OH:10])=[O:9].[N+:1]([O-:4])([OH:3])=[O:2].[N+:1]([O-:4])([OH:3])=[O:2].[N+:1]([O-:4])([OH:3])=[O:2].[NH2:15][CH2:16][CH2:17][C:18]([OH:20])=[O:19]

Participants

6

Procedure

Applicants have cost-effectively synthesized Beta Alanine Nitrate by combining nitric acid and Beta Alanine, mixing with water, and leaving to crystallize. Further nitratization can take place, yielding Beta Alanine Dinitrate or Beta Alanine Trinitrate. An alternative implementation comprises using Nitrous Acid (HNO2) instead of Nitric Acid (HNO3), thus yielding Beta Alanine Nitrite. Beta Alanine Nitrite has the same effects as Beta Alanine Nitrate, the only difference being that it requires one less step to yield Nitric Oxide (NO—). Mixed salts may also be used, such as in the non-limiting example of Beta Alanine Nitrate-Orotate.

Workup

  1. customleaving
  2. customto crystallize

Sources & evidence

ORD record
ord-e3803ae476a543bf8a0c47a52580b742
Source dataset
uspto-grants-2015_02
Patent number
US08952047B1

Reaction notes

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