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A propos de cet article
Formule linéaire :
Li
Numéro CAS:
Poids moléculaire :
6.94
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12141803
EC Number:
231-102-5
MDL number:
Service technique
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99.9% trace metals basis
form
rod
reaction suitability
core: lithium, reagent type: reductant
resistivity
9.446 μΩ-cm, 20°C
diam.
12.7 mm
bp
1342 °C (lit.)
mp
180 °C (lit.)
density
0.534 g/mL at 25 °C (lit.)
application(s)
battery manufacturing
SMILES string
[Li]
InChI
1S/Li
InChI key
WHXSMMKQMYFTQS-UHFFFAOYSA-N
General description
Our high-purity lithium rod with a diameter of 12.7 mm is a cylindrical piece of metal made of lithium, a highly reactive, silvery-white metal. Lithium is one of the lightest and most electropositive metals, making it highly reactive. Lithium is a good conductor of electricity and heat, has a low melting point (180 °C), and is soft and ductile.
Application
Lithiummetal is widely used to fabricate anode material for rechargeable batteries dueto its low negative electrochemical potential and high theoretical specificcapacity.
signalword
Danger
hcodes
supp_hazards
Classe de stockage
4.3 - Hazardous materials which set free flammable gases upon contact with water
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Hazard Classifications
Skin Corr. 1B - Water-react. 1
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The number of chromosome sets contained within the nucleus of eukaryotic organisms is a fundamental yet evolutionarily poorly characterized genetic variable of life. Here, we mapped the impact of ploidy on the mitotic fitness of baker's yeast and its never
Dongyun Chen et al.
Nanoscale, 5(17), 7890-7896 (2013-07-16)
Two-dimensional nanosheets can leverage on their open architecture to support facile insertion and removal of Li(+) as lithium-ion battery electrode materials. In this study, two two-dimensional nanosheets with complementary functions, namely nitrogen-doped graphene and few-layer WS2, were integrated via a
Sureshbabu Guduguntla et al.
The Journal of organic chemistry, 78(17), 8274-8280 (2013-08-22)
An efficient one-pot synthesis of optically active β-alkyl-substituted alcohols through a tandem copper-catalyzed asymmetric allylic alkylation (AAA) with organolithium reagents and reductive ozonolysis is presented. Furthermore, hydroboration-oxidation following the Cu-catalyzed AAA leads to the corresponding homochiral γ-alkyl-substituted alcohols.

