449873
Lithium bromide
AnhydroBeads™, −10 mesh, ≥99.9% trace metals basis
동의어(들):
Lithium monobromide
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제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
LiBr
CAS 번호:
Molecular Weight:
86.85
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12352302
EC Number:
231-439-8
MDL number:
Assay:
≥99.9% trace metals basis
Grade:
synthesis grade
grade
synthesis grade
product line
AnhydroBeads™
assay
≥99.9% trace metals basis
reaction suitability
core: lithium
impurities
≤1000.0 ppm Trace Metal Analysis
particle size
−10 mesh
mp
550 °C (lit.)
application(s)
battery precursors
catalysts
material synthesis precursor
SMILES string
[Li+].[Br-]
InChI
1S/BrH.Li/h1H;/q;+1/p-1
InChI key
AMXOYNBUYSYVKV-UHFFFAOYSA-M
Legal Information
AnhydroBeads is a trademark of Sigma-Aldrich Co. LLC
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1
저장 등급
11 - Combustible Solids
wgk
WGK 2
flash_point_f
No data available
flash_point_c
No data available
문서
Solid-state lithium fast-ion conductors are crucial for safer, high-energy-density all-solid-state batteries, addressing conventional battery limitations.
Ngoc-Ly Hoang et al.
Journal of chromatography. A, 1205(1-2), 60-70 (2008-08-30)
The structure of starch molecules is relevant to nutrition and industrial applications. Size-exclusion chromatography (SEC, also known as GPC) of native starch generally suffers non-satisfactory repeatability and reproducibility of the dissolution and separation. This work combines two polar organic solvents:
Mohammad M Mojtahedi et al.
Organic letters, 9(15), 2791-2793 (2007-06-22)
A room temperature convenient disproportionation or reduction of aldehydes prompted by lithium bromide and triethylamine is described in a solvent-free environment. Distribution of the products to selectively direct the process toward Cannizzaro or Tishchenko reactions is controlled by the type
R Quaderer et al.
Organic letters, 3(20), 3181-3184 (2001-09-28)
[reaction: see text] The alkanesulfonamide "safety-catch" resin has proven useful for Fmoc-based synthesis of C-terminal peptide thioesters. We now report that the yield of isolated thioester can increase significantly when the cleavage reaction is carried out in 2 M LiBr/THF