Aniline nitrate

Base Information

• Chemical Name: Aniline nitrate
• CAS No.: 542-15-4
• Molecular Formula: C6H8N2O3
• Molecular Weight: 156.141
• Hs Code.: 2921419000
• European Community (EC) Number: 208-804-5
• UNII: 4C4E2X9L3U
• Wikidata: Q27259398
• ChEMBL ID: CHEMBL3392014
• Mol file: 542-15-4.mol

Synonyms:aniline;aniline aluminium salt;aniline dihydrofluoride;aniline diphosphate (1:1);aniline diphosphate (3:1);aniline diphosphate (4:1);aniline hydrobromide;aniline hydrochloride;aniline hydrochloride-(14)C-labeled cpd;aniline hydrochloride-(15)N-labeled cpd;aniline hydrofluoride;aniline hydrogen iodide;aniline monosulfate;aniline nitrate;aniline perchlorate;aniline phosphate (1:1);aniline phosphate (1:2);aniline phosphate (2:1);aniline phosphonate (1:1);aniline sulfate;aniline sulfate (2:1);aniline sulfate (2:1), (14)C-labeled cpd;aniline, (13)C-labeled cpd;aniline, (14)C-labeled cpd;aniline, 15N-labeled cpd;aniline, 2-(13)C-labeled cpd;aniline, 3-(13)C-labeled cpd;aniline, 3H-labeled cpd;aniline, 4-(13)C-labeled cpd;aniline, conjugate acid;aniline, ion(1+);aniline, magnesium (1:1) salt;aniline, monolithium salt;aniline, sodium salt

Chemical Property of Aniline nitrate

Chemical Property:

• Vapor Pressure: 0.733mmHg at 25°C
• Melting Point: 190°C (rough estimate)
• Refractive Index: ">
• Boiling Point: 184.4°Cat760mmHg
• Flash Point: 70°C
• PSA: 92.07000
• Density: g/cm³
• LogP: 2.02550
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 0
• Exact Mass: 156.05349212
• Heavy Atom Count: 11
• Complexity: 70.9

Purity/Quality:

98%min ^*data from raw suppliers

ANILINE NITRATE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)N.[N+](=O)(O)[O-]

Technology Process of Aniline nitrate

There total 9 articles about Aniline nitrate 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: 98.0%

aniline (62-53-3) → anilinium nitrate (542-15-4)

Guidance literature:

With nitric acid; In tert-butyl methyl ether; water; at 0 - 20 ℃; for 1h;

Reference yield:

chloroform (67-66-3,8013-54-5) + benzylidene phenylamine (538-51-2) → benzenediazonium nitrate (619-97-6) + 3-nitro-benzaldehyde (99-61-6) + anilinium nitrate (542-15-4) + benzaldehyde (100-52-7)

Guidance literature:

Prod_.5:p-Benzalamino-azobenzol;

Reference yield:

nitric acid (7697-37-2,78989-43-2) + aniline (62-53-3) → anilinium nitrate (542-15-4)

Guidance literature:

with dild. HNO3;

upstream raw materials:

tetrachloromethane

nitro acetate

aniline

ethyl nitrate

Downstream raw materials:

phenylguanidine nitrate

4-nitro-aniline

2-nitro-aniline

3-nitro-aniline