Nitraminoacetic acid

Base Information

Chemical Name:Nitraminoacetic acid
CAS No.:10339-31-8
Molecular Formula:C2H4 N2 O4
Molecular Weight:120.065
Hs Code.:2922499990
DSSTox Substance ID:DTXSID00145809
Wikidata:Q83010456
Metabolomics Workbench ID:98043
Mol file:10339-31-8.mol

Synonyms:nitraminoacetate;nitraminoacetic acid

Suppliers and Price of Nitraminoacetic acid

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
2-(Nitroamino)aceticAcid
25mg
$ 350.00

Total 8 raw suppliers

Chemical Property of Nitraminoacetic acid

Chemical Property:

Vapor Pressure:8E-06mmHg at 25°C
Melting Point:106°C
Refractive Index:1.4264 (estimate)
Boiling Point:349.7°Cat760mmHg
Flash Point:165.3°C
PSA：95.15000
Density:1.543g/cm³
LogP:-0.23360
XLogP3:0.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:2
Exact Mass:120.01710661
Heavy Atom Count:8
Complexity:105

Purity/Quality:

98%,99%, ^*data from raw suppliers

2-(Nitroamino)aceticAcid ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C(C(=O)O)N[N+](=O)[O-]

Technology Process of Nitraminoacetic acid

There total 2 articles about Nitraminoacetic acid 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:

: 10339-31-8
carboxymethyl-N-nitroamine

Guidance literature:: With diethyl ether; ammonia; man zersetzt das Ammoniumsalz mit verd. Schwefelsaeure und verseift den Ester durch methylalkoholische Kalilauge unter Kuehlung;