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703508

Sigma-Aldrich

Lithium aluminum hydride solution

greener alternative

2.3 M in 2-methyltetrahydrofuran

Sinónimos:

LAH, Lithium alanate, Lithium tetrahydroaluminate

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About This Item

Fórmula lineal:
LiAlH4
Número de CAS:
16853-85-3
Peso molecular:
37.95
Número MDL:
MFCD00011075
Código UNSPSC:
26111700
ID de la sustancia en PubChem:
329762044
NACRES:
NA.22

Formulario

liquid

Nivel de calidad

200

idoneidad de la reacción

reagent type: reductant

características de los productos alternativos más sostenibles

Safer Solvents and Auxiliaries
Use of Renewable Feedstocks
Inherently Safer Chemistry for Accident Prevention
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

concentración

10 % (w/w)
2.3 M in 2-methyltetrahydrofuran

densidad

0.883 g/mL at 25 °C

categoría alternativa más sostenible

, Aligned

temp. de almacenamiento

2-30°C

cadena SMILES

[Li+].[AlH4-]

InChI

1S/Al.Li.4H/q-1;+1;;;;

Clave InChI

OCZDCIYGECBNKL-UHFFFAOYSA-N

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Descripción general

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product, 2.3 M in 2-methyltetrahydrofuran aligns with Safer Solvents and Auxiliaries, Use of Renewable Feedstocks and Inherently Safer Chemistry for Accident Prevention. Click here for more information.

Aplicación

Powerful reducing agent in greener solvent, 2-methyltetrahydrofuran (2-MeTHF).

2-Methyltetrahydrofuran (2-MeTHF): A Biomass-Derived Solvent with Broad Application in Organic Chemistry
Reactant or reagent for:
  • The preparation of thermoplastic polyester polyamides from oleic acid
  • Lithium-polymer batteries
  • Hydrodefluorination of gem-difluoromethylene derivatives
  • Asymmetric aldol reactions
  • Synthesis of Li-Al-N-H composites with hydrogen absorption / desorption properties

LAH is a powerful reducing agent for many different reduction reactions such as that of ketones to alcohols

Palabra de señalización

Danger

Frases de peligro

H225,H260,H302,H314

Clasificaciones de peligro

Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1A - Water-react 1

Riesgos supl.

EUH019

Código de clase de almacenamiento

4.3 - Hazardous materials which set free flammable gases upon contact with water

Clase de riesgo para el agua (WGK)

WGK 2

Punto de inflamabilidad (°F)

10.4 °F - closed cup - Solvent

Punto de inflamabilidad (°C)

-12 °C - closed cup - Solvent

Equipo de protección personal

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificados de análisis (COA)

Lot/Batch Number
SHBR5153
SHBP5329
SHBP6864
SHBN4600
SHBM7107

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Si necesita una versión concreta, puede buscar un certificado específico por el número de lote.

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Haruki Sashida et al.
Chemical & pharmaceutical bulletin, 52(1), 57-62 (2004-01-08)
The reactions of the 2-benzoselenopyrylium (1A) and 2-benzotelluropyrylium cations (1B) with a variety of nucleophiles have been investigated. LiAlH(4), sodium alkoxide (NaOMe, NaOi-Pr and NaOt-Bu), diethylamine, n-butylamine and acetone reacted with 1 to give the 1H-isochromenes (2) and the corresponding
José M Concellón et al.
The Journal of organic chemistry, 71(17), 6420-6426 (2006-08-12)
The reaction of chiral (2R,1'S)- or (2S,1'S)-2-(1-aminoalkyl)epoxides, 1 or 2 with a variety of organolithium compounds to obtain the corresponding (alphaS,betaS)- or (alphaR,betaS)- beta-amino alcohols in enantiopure form is reported. In both cases, the opening of the oxirane ring at
Hao Yao et al.
Journal of electron microscopy, 60(6), 375-378 (2011-10-05)
A plastic bag method was developed to observe air-sensitive samples on microstructure and phase distribution without exposure to air during the holder transfer process into the transmission electron microscope (TEM). As an example, a type of lithium aluminum hydride (Li(3)AlH(6))
Takashi Ikegami et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 804(1), 197-201 (2004-04-20)
Bisphenol A (BPA) recognition materials were synthesized by a covalent imprinting technique using BPA-dimethacrylate or BPA-diacrylate as the template monomer. Binding sites in the polymers consisted of two hydroxyl groups that are generated by reducing the ester bonds of the
I-Chi Lee et al.
Organic & biomolecular chemistry, 9(22), 7655-7658 (2011-09-17)
Specific deuterated reference compounds were prepared to probe the stereoselectivity of the reductive ring opening of carbohydrate-based benzylidene-type acetals. AlD(3) revealed a retentive stereoselectivity probably through the rare S(N)i (internal nucleophilic substitution) mechanism. An S(N)1-like mechanism occurs in the acid-promoted
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