310468
Cloruro de litio
ACS reagent, ≥99%
About This Item
Productos recomendados
grade
ACS reagent
Quality Level
assay
≥99%
form
crystalline powder
powder, crystals or granules
impurities
≤0.008 meq/g Titr. base
≤0.01% insolubles
loss
≤1.0% loss on drying
pH
6
mp
605 °C (lit.)
anion traces
sulfate (SO42-): ≤0.01%
cation traces
Ba: ≤0.003%
Ca: ≤0.01%
Fe: ≤0.001%
K: ≤0.01%
Na: ≤0.20%
heavy metals: ≤0.002% (by ICP)
SMILES string
[Li+].[Cl-]
InChI
1S/ClH.Li/h1H;/q;+1/p-1
InChI key
KWGKDLIKAYFUFQ-UHFFFAOYSA-M
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General description
Application
- A source of chloride anion for the conversion of alcohols to alkyl chloride under Mitsunobu conditions.
- An additive in the palladium-catalyzed coupling and carbonylative coupling reactions of organostannanes and vinyl triflates.
- A reagent for the cleavage of protecting groups under mild conditions. It readily converts acetals and ketals to the corresponding carbonyl compounds.
- A reagent in the dehydrohalogenation of α-halocarbonyl compounds to α,β-unsaturated carbonyls compound in the presence of DMF.
LiCl is also used with other reagents:
- LiCl:DIPEA (1:1 molar ratio) is used in Horner–Wadsworth–Emmons alkenation reaction.
- LiCl:Hexamethylphosphoric triamide is used in decarboxylative alkylation and chloride displacement reactions.
- LiCl is used as an additive in solid-phase peptide synthesis because it increases resin swelling and improves the efficiencies of complex coupling steps.
Features and Benefits
- Easy to handle
- Weak Lewis acid
- Highly soluble in water
Other Notes
Legal Information
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2
Storage Class
13 - Non Combustible Solids
wgk_germany
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
Certificados de análisis (COA)
Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»
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Artículos
Transformative reagents enable selective conversions within molecules containing sensitive functionalities under mild reactions.
Transformative reagents enable selective conversions within molecules containing sensitive functionalities under mild reactions.
Transformative reagents enable selective conversions within molecules containing sensitive functionalities under mild reactions.
Transformative reagents enable selective conversions within molecules containing sensitive functionalities under mild reactions.
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