Methyllithium

HCID 2724049CAS 917-54-4

Grundinformationen

Standard-SMILES
[CH3-].[Li+]
InChIKey
DVSDBMFJEQPWNO-UHFFFAOYSA-N
Summenformel
CH3Li
Durchschnittliche Molmasse
22 g/mol

Überblick

Methyllithium is an alkyllithium compound and a one-carbon compound.

Namen und Bezeichner

Bevorzugter Name
Methyllithium
IUPAC
lithium carbanide
Lokaler Name
Methyllithium
Englischer Name
Methyllithium
Summenformel
CH3Li
Molmasse
21.98

Namen und Synonyme

Methyllithium917-54-4Lithium, methyl-lithium;carbanideLithium methideMethyl lithiumMeLiCH3LimethllithiummethyllithummethyllitiumMFCD00008253
Weitere Namen anzeigen
LITHIUM METHANIDEMethyllithium lithium bromide complex solutionMethyllithium solutionLowhalide1-2MinEthermethyl-lithiuMethy-LithiumLITHIUM METHYL
Methyl-lithiumEINECS 213-026-4EC 213-026-4SCHEMBL4929Methyllithium 1.6m in etherSCHEMBL5422193SCHEMBL9381060DTXSID7061273

Datenbank-Bezeichner

CAS
917-54-4
PubChem CID
2724049
DTXSID
DTXSID7061273
ChEBI
CHEBI:51486
Nikkaji
J1.231I

Eigenschaften

Berechnete Struktureigenschaften

Polarare Oberfläche (TPSA)
0 Ų
H-Brücken-Donoren
0
H-Brücken-Akzeptoren
1
Frei drehbare Bindungen
0
Schwere Atome
2

Physikochemische Eigenschaften

Schmelzpunkt
70 · 70-71℃
Siedepunkt
88 ℃ · 88℃
Dichte
0.85 g/mL · 0.85 g/mL at 20 °C
Dampfdichte
3 · 3 (vs air)
Flammpunkt
5 °F · 5 °F
storage temp.
2 · 2-8°C

Sicherheit und Regulatorisches

Sicherheitsdaten

F
10
wgk
2
tsca
TSCA listed
ridadr
UN 3399 4.3/PG 1
hs_code
29319090
risk_code
12-15-17-22-34-66-67-65-51/53-11-36/37/38-36/38-19-40-36/37-37-14/15

Chemie und Industrie

Anwendungen · 1 Eintrag

VerwendenThere are no significant industrial uses of methyllithium, but it is widely used in the laboratory in Grignard type reactions. Methyllithium is an organolithium reagent mainly used for deprotonation and as a source of methyl anion. It is a strong base and a strong nucleophile.

Darstellung · 1 Eintrag

synthetischeMethyllithium is produced industrially by the reaction of methyl chloride or methyl bromide with lithium metal dispersion in diethyl ether. The reaction with methyl chloride yields a solution of methyllithium and a precipitate of lithium chloride which may be readily separated. When methyl bromide is used, the lithium bromide byproduct remains in solution and complexes with the methyllithium. This reduces the reactivity of the methyllithium and, in certain cases, affects its usefulness. On the other hand, the less reactive complex is more stable in diethyl ether. Methyllithium produced from methyl chloride contains only about 0.3 % lithium chloride in a 5 % solution in diethyl ether. It is more reactive than the lithium bromide complex, but decomposes at the rate of 1 % of the contained methyllithium per year (that is 5.00 % solution goes to 4.95 %) at room temperature. The decomposition by ether cleavage results in methane and ethylene formation which increases the pressure in the container on long storage. Methyllithium can be prepared easily in tetrahydrofuran but it has a half-life of only about 2 days at room temperature due to solvent cleavage.

Anbieter50 Anbieter

国药集团化学试剂有限公司86-21-63210123 · [email protected]
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梯希爱(上海)化成工业发展有限公司021-67121386 · [email protected]
山东旭晨化工科技有限公司0533-15715337262 15715337262 · [email protected]
Shandong chuangyingchemical Co., Ltd.18853181302 · [email protected]

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