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Lanthanum(III) chloride bis(lithium chloride) complex solution_Molecular_structure_CAS_405204-22-0)
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Lanthanum(III) chloride bis(lithium chloride) complex solution

Catalog No. 703559 Name Sigma Aldrich
CAS Number 405204-22-0 Website http://www.sigmaaldrich.com
M. F. Cl5LaLi2 Telephone 1-800-521-8956
M. W. 330.0525 Fax
Purity Email
Storage Chembase ID: 141064

SYNONYMS

Title
氯化镧(III)双(氯化锂)络合物 溶液
IUPAC name
bis(chlorolithium); trichlorolanthanum
IUPAC Traditional name
lanthanum(III) chloride; bis(lithium chloride)
Synonyms
三氯化镧氯化锂络合物
Lanthanum trichloride lithium chloride complex

DATABASE IDS

CAS Number 405204-22-0

PROPERTIES

Concentration 0.6 M in THF
Concentration 16 % (w/w)
Linear Formula LaCl3 · 2LiCl
Density 1.05 g/mL at 25 °C
Flash Point 17 °C
Flash Point 62.6 °F
GHS Pictograms GHS02
GHS Pictograms GHS07
GHS Pictograms GHS09
GHS Signal Word Danger
GHS Hazard statements H225-H315-H319-H335-H400
European Hazard Symbols Flammable Flammable (F)
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment Eyeshields, Faceshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
GHS Precautionary statements P210-P261-P273-P305 + P351 + P338
RID/ADR UN 2056 3/PG 2
Risk Statements 11-19-36/37/38
Safety Statements 16-26
Supplemental Hazard Statements May form explosive peroxides.
Hazard Class 3
UN Number 2056
Packing Group 2
German water hazard class 3

DETAILS

Description (English)
Packaging
100 mL in Sure/Seal™
Legal Information
Product of Rockwood Lithium
Application
Selective 1,2-Additions with LaCl3
•2LiCl
• Mediates Grignard additions1
• Reagent for metal exchange reactions2
• Promoter for the addition of organometallic compounds to sterically hindered, enolizable or α,β-unsaturated ketones or imines3
Description (简体中文)
包装
100 mL in Sure/Seal™
Legal Information
Product of Rockwood Lithium
Application
Selective 1,2-Additions with LaCl3
•2LiCl
• Mediates Grignard additions1
• Reagent for metal exchange reactions2
• Promoter for the addition of organometallic compounds to sterically hindered, enolizable or α,β-unsaturated ketones or imines3

REFERENCES