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Lithium amide

Base Information Edit
  • Chemical Name:Lithium amide
  • CAS No.:7782-89-0
  • Deprecated CAS:12135-17-0,1808075-59-3,2691865-42-4
  • Molecular Formula:LiNH2
  • Molecular Weight:22.96
  • Hs Code.:2836.91
  • European Community (EC) Number:231-968-4
  • UN Number:3134,1412
  • UNII:7393OMU9LK
  • DSSTox Substance ID:DTXSID7064815
  • Nikkaji Number:J71.254J
  • Wikipedia:Lithium_amide
  • Wikidata:Q2565173
  • Mol file:7782-89-0.mol
Lithium amide

Synonyms:LITHIUM AMIDE;7782-89-0;Lithamide;lithium;azanide;Lithium amide (Li(NH2));UNII-7393OMU9LK;7393OMU9LK;HSDB 649;EINECS 231-968-4;Lithiumamide;lithium azanide;MFCD00011093;H2LiN;LiNH2;H2-Li-N;LITHIUM AMIDE [MI];LITHIUM AMIDE [HSDB];Amida de litio (li (nh2));Lithium amide, powder, 95%;DTXSID7064815;NA1412;UN1412;Lithium amide, hydrogen-storage grade;AKOS030228593;FT-0627889;Q2565173

Suppliers and Price of Lithium amide
Supply Marketing:Edit
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
  • Usbiological
  • Lithium amide
  • 25g
  • $ 456.00
  • Strem Chemicals
  • Lithium amide, 95%
  • 50g
  • $ 45.00
  • Strem Chemicals
  • Lithium amide, 95%
  • 250g
  • $ 181.00
  • Sigma-Aldrich
  • Lithium amide hydrogen-storage grade
  • 10g
  • $ 78.90
  • Sigma-Aldrich
  • Lithium amide powder, 95%
  • 100g
  • $ 63.00
  • Sigma-Aldrich
  • Lithium amide powder, 95%
  • 5g
  • $ 36.80
  • Sigma-Aldrich
  • Lithium amide powder, 95%
  • 500g
  • $ 214.00
  • Chem-Impex
  • Lithium amide, 95% ≥95%
  • 100KG
  • $ 16889.60
  • Chem-Impex
  • Lithium amide, 95% 95%
  • 25KG
  • $ 7616.01
  • American Custom Chemicals Corporation
  • LITHIUM AMIDE 95.00%
  • 100G
  • $ 2515.93
Total 40 raw suppliers
Chemical Property of Lithium amide Edit
Chemical Property:
  • Appearance/Colour:White crystals 
  • Melting Point:373 °C 
  • Refractive Index:1.178g/mL 
  • Boiling Point:430 °C 
  • PSA:26.02000 
  • Density:1.178 g/mL at 25 °C(lit.) 
  • LogP:0.10970 
  • Storage Temp.:water-free area 
  • Sensitive.:Air & Moisture Sensitive 
  • Solubility.:Slightly soluble in ethanol and liquid ammonia. Insoluble in anh 
  • Water Solubility.:reacts 
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:0
  • Exact Mass:23.03472750
  • Heavy Atom Count:2
  • Complexity:2
  • Transport DOT Label:Dangerous When Wet Poison
Purity/Quality:

99.9% *data from raw suppliers

Lithium amide *data from reagent suppliers

Safty Information:
  • Pictogram(s): FlammableF,Corrosive
  • Hazard Codes:F,C 
  • Statements: 14/15-29-34-20/21/22-15-14-11 
  • Safety Statements: 26-36/37/39-43-45-7/8-43B-16-3/7/9 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Chemical Classes:Other Classes -> Bases
  • Canonical SMILES:[Li+].[NH2-]
  • Physical properties Colorless needles; tetragonal structure; density 1.178 g/cm3 at 17.5°C; melts around 375°C; starts to decompose at 320°C; decomposes at 400°C; soluble in cold water; decomposes in hot water; slightly soluble in ethanol and liquid ammonia; insoluble in benzene and ether.
  • Uses Lithium amide is used in the preparation of active pharmaceutical ingredients and antioxidants. It acts as a catalyst for polymers, as nucleophiles and as strong bases. It serves as a reagent in the synthesis of antiinflamatory and preoresolving protectin D1, chemotype dipeptidyl peptidase IV inhibitors and sterically congested triarylamines. It finds application in dyes displaying large stokes shifts. In addition to this, it is used as a reagent for cross-coupling of aryl chlorides and amine. Reagent for synthesis of: Antiinflamatory and preoresolving protectin D11 Chemotype dipeptidyl peptidase IV inhibitors2 Sterically congested triarylamines3 Dyes displaying large Stokes shifts4 GM1 ganglioside derivatives5Reagent for cross-coupling of aryl chlorides and amines6 In Claisen condensations, alkylation of nitriles and ketones, synthesis of ethynyl Compounds, acetylenic carbinols.
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