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Merck
모든 사진(4)

주요 문서

205281

Sigma-Aldrich

Lithium perchlorate

ACS reagent, ≥95.0%

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About This Item

Linear Formula:
LiClO4
CAS Number:
Molecular Weight:
106.39
EC Number:
MDL number:
UNSPSC 코드:
12352302
PubChem Substance ID:
NACRES:
NA.21
분석:
≥95.0%
Grade:
ACS reagent
양식:
powder, chunks or granules

Grade

ACS reagent

Quality Level

분석

≥95.0%

양식

powder, chunks or granules

반응 적합성

reagent type: oxidant

불순물

≤0.005% insolubles

pH

6.0-7.5 (25 °C, 5%)

mp

236 °C (lit.)

음이온 미량물

chloride (Cl-): ≤0.003%
sulfate (SO42-): ≤0.001%

양이온 미량물

Fe: ≤5 ppm
heavy metals: ≤5 ppm (by ICP-OES)

SMILES string

[Li+].[O-]Cl(=O)(=O)=O

InChI

1S/ClHO4.Li/c2-1(3,4)5;/h(H,2,3,4,5);/q;+1/p-1

InChI key

MHCFAGZWMAWTNR-UHFFFAOYSA-M

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일반 설명

Lithium perchlorate (LiClO4) is a colorless lithium salt. On the crystallization from its aqueous solution, it affords lithium perchlorate trihydrate (LiClO4.3H2O). It can be synthesized by reacting lithium chloride with perchloric acid.

애플리케이션

Lithium perchlorate (LiClO4) may be used as a catalyst in the synthesis of bis(indolyl)methanes.
Lithium perchlorate may be used to catalyze:
  • The acylation of hindered alcohols and phenols under solvent-free conditions.
  • 1,4-Conjugate addition of O-silylated ketene acetals to hindered αβ,-unsaturated carbonyl system.
  • The protection of amine groups as N-Boc derivatives via tert-butoxycarbonylation.
  • Synthesis of α-aminophosphonates under solvent free conditions.
When used as a co-catalyst, accelerates the Baylis-Hillman reaction, the coupling of α,β-unsaturated carbonyls with aldehydes.

픽토그램

Flame over circleCorrosionExclamation mark

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Ox. Sol. 2 - Skin Corr. 1A - STOT SE 3

표적 기관

Respiratory system

Storage Class Code

5.1A - Strongly oxidizing hazardous materials

WGK

WGK 1

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


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문서 라이브러리 방문

Lithium perchlorate catalyzed acetylation of alcohols under mild reaction conditions.
Nakae Y, et al.
Synlett, 2001(10), 1584-1586 (2001)
Lithium Perchlorate-Catalyzed Boc Protection of Amines and Amine Derivatives.
Heydari A and Hosseini SE.
Advanced Synthesis & Catalysis, 347(15), 1929-1932 (2005)
Lithium Perchlorate-Catalyzed Three-Component Coupling: A Facile and General Method for the Synthesis of a-Aminophosphonates under Solvent-Free Conditions.
Azizi N and Saidi MR.
European Journal of Organic Chemistry, 2003(23), 4630-4633 (2003)
Lithium perchlorate catalyzed conjugate addition of O-silylated ketene acetals to hindered a, ?-unsaturated carbonyl compounds at atmospheric pressure.
Grieco PA, et al.
Tetrahedron Letters, 32(36), 4665-4668 (1991)
Lithium perchlorate catalyzed reactions of indoles: An expeditious synthesis of bis (indolyl) methanes.
Yadav JS, et al.
Synthesis, 2001(5), 0783-0787 (2001)

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