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HCID 3474584Erstellt: 26. Oktober 2026

Lithiumacetat

quilone · Lithiumacetat · ithium acetate · LITHIUM ACETATE · lithiumethanate · Lithiumethanoat · lithiumethanoate · LithiumAcetate>Acetic acid lithium

https://huagongshe.com/de/chemical/3474584

Molekülstruktur von Lithiumacetat

Identifikatoren & physikalische Daten

CAS No.546-89-4
SummenformelC2H3LiO2
Durchschnittliche Molmasse66 g/mol
Monoisotopische Masse66,02930889 g/mol
SMILESCC(=O)[O-].[Li+]
InChIKeyXIXADJRWDQXREU-UHFFFAOYSA-M
PubChem CID3474584
ChEBICHEBI:63045
EC No.208-914-3
DTXSIDDTXSID00883436
Lokaler NameLithiumacetat

Chemische & physikalische Eigenschaften

Polarare Oberfläche (TPSA)40,1
H-Brücken-Donoren0
H-Brücken-Akzeptoren2
Frei drehbare Bindungen0
Schwere Atome5
Formalladung0
Komplexität34,6
StoffklassenMetals -> Organic Acids, Metal Salts
Dichte1.28 @ 20°C1.3[at 20℃]
Schmelzpunkt280 °C283-285 °C (lit.)
Physical DescriptionOther SolidBecomes dihydrate at 56.5 deg C[Merck Index] White powderSoluble in water[MSDSonline]
Dampfdruck0Pa at 25℃
LagerbedingungenInert atmosphere,Room Temperature
LöslichkeitH2O: 5 M at 20 °C, clear, colorless40.8 g/100 mL (20 ºC)
AggregatzustandPowder or Crystals
FarbeWhite to yellow
Merck14,5521
StabilitätStable. Incompatible with strong oxidizing agents.
Hauptanwendungenbattery precursorscatalystsmaterial synthesis precursor
InChIInChI=1S/C2H4O2.Li/c1-2(3)4/h1H3,(H,3,4)/q+1/p-1
InChIKeyXIXADJRWDQXREU-UHFFFAOYSA-M
SMILESC([O-])(=O)C.[Li+]
LogP (Verteilungskoeffizient)0.09 at 25℃
CAS Datenbank546-89-4(CAS DataBase Reference)
EPA chemische InformationenLithium acetate (546-89-4)

Sicherheit & Vorschriften

GHS-EinstufungThis chemical does not meet GHS hazard criteria for 29.7% (102 of 343) of reports.WarningH302 (64.7%): Harmful if swallowed [Warning Acute toxicity, oral]P264, P264+P265, P270, P280, P301+P317, P305+P351+P338, P330, P337+P317, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 343 reports by companies from 8 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Regulatorische InformationenChemical: Acetic acid, lithium saltAcetic acid, lithium salt (1:1) is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Acetic acid, lithium salt (1:1) are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)Status: Active Update: 13-03-2019 https://echa.europa.eu/registration-dossier/-/registered-dossier/21532Acetic acid, lithium salt: Does not have an individual approval but may be used under an appropriate group standard
Weitere SicherheitsinformationenIMAP assessments - Acetic acid, lithium salt: Human health tier I assessment
GefahrenübersichtMay cause irritationAffects the central nervous system when used as a drug[MSDSonline] See Lithium.
Hazard Classes and CategoriesAcute Tox. 4 (64.7%)
Expositionsschutz und Persönliche Schutzausrüstung0.2 [mg/m3], inhalable fraction, as Li[German Research Foundation (DFG)]
Protective Action Criteria (PAC)3.2 [mg/m3]36 [mg/m3]210 [mg/m3]
Unerwünschte WirkungenNeurotoxin - Other CNS neurotoxin
Wassergefährdungsklasse (WGK)1
TSCA-Inventar-StatusTSCA listed
Zollcode29152990
RTECS-Nr.AI5450000
R-Sätze (R)36
GefahrensymboleXi
Sicherheitshinweise (S)23-24/25-39-26-22
Lagerklasse11 - Combustible Solids
GefahrenklasseAcute Tox. 4 OralEye Irrit. 2

Anwendungen & Verwendung

Beschreibung

Lithium acetate (CH3COOLi) is a salt of lithium and acetic acid.

Verwenden

Lithium acetate is used in the laboratory as buffer for gel electrophoresis of DNA and RNA. It has a lower electrical conductivity and can be run at higher speeds than can gels made from TAE buffer (5-30V/cm as compared to 5 - 10 V / cm). Lithium boric acid or sodium boric acid are usually preferable to lithium acetate or TAE when analyzing smaller fragments of DNA (less than 500 bp) due to the higher resolution of borate-based buffers in this size range as compared to acetate buffers. Lithium acetate is also used to permeabilize the cell wall of yeast for use in DNA transformation. It is believed that the beneficial effect of LiAc is caused by its chaotropic effect denaturing both DNA, RNA and proteins.