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Flammability 2 Must be moderately heated or exposed to relatively high ambient temperatures before ignition can occur.
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Lithium aluminum hydride LiAlH 4 is an effective reducing agent that can be used in chemical synthesis to buy lithium aluminum hydride esters, carboxylic acids, acyl chlorides, aldehydes, epoxides, and ketones into the corresponding alcohols. Lithium aluminum hydride LAH, as well as other aluminum and boron hydrides lose their activity due to interaction with moist, oxygen and CO 2 even under good storing conditions. Discarding of such deteriorated reagents is neither economical or safe nor environmentally sound. We are one of largest marine chemical manufacturing company in Asia.
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The growth is attributed to the increased use of LAH in the automotive industry and the surging buy lithium aluminum hydride for fuel cells. Competitive landscape highlights only certain players Complete list available upon request. It is widely utilized for the reduction of carboxylic acids and esters for their primary alcohols.
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Reducing agent for pharmaceuticals, perfumes and fine organic chemicals; source of hydrogen, propellant, and catalyst in polymerizationsLithium aluminum hydride is used as a reducing agent in various synthetic organic chemistry reactions. It reacts with sodium chloride to prepare sodium hydride. It acts as a potential hydrogen storage medium, which could be used for future fuel cell-powered vehicles. It is mainly used in the preparation of other tetrahydridoaluminumates like sodium aluminum hydride, potassium aluminum hydride and magnesium alanate.
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It is a strong reducing agent used in organic chemistry. LAH is sensitive to water, and reacts vigorously to release hydrogen. LAH is a strong reducing agent, it will buy lithium aluminum hydride esters, carboxylic acids, acyl chlorides, aldehydes, and ketones into the corresponding alcohols. Similarly, it converts amide, azide, imine, nitrile, nitro and oxime compounds into amines. LAH is most commonly used for the reduction of esters and carboxylic acids to primary alcohols.
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Lithium aluminum hydride is much too powerful a reducing agent to stop the reduction of acyl halides at the aldehyde stage and further reduction to alcohol is the usual result. From: Comprehensive Organic Synthesis, Smalley, in Comprehensive Heterocyclic Chemistry, Keay, in Comprehensive Organic Synthesis, Lithium aluminum hydride LAH reacts with pyridines and their analogs in aprotic solvents to give dihydro- and tetrahydro-pyridines.
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Lithium aluminium hydride Cat. Attention: For buy lithium aluminum hydride use only. Not for human or veterinary use. It is an important reagent in organic synthesis and a versatile reducing agent used in many laboratory experiments. LAH is a white, crystalline solid with a pungent odor.
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Standard Search Advanced Search. Mechanism of lithium aluminum hydride reduction of ketones.
- The anhydride may be prepared by reacting lithium hydride with aluminum chloride.
- Lithium hydride is a simple neutral heteropolar diatomic molecule.
- It was discovered by Finholt, Bond and Schlesinger in
- Lithium aluminum hydride LiAlH 4 is a strong reducing agent with a particular utility for carboxylic acid derivatives.
- LiAlH 4 is a very common, strong reducing agent, which reduces a vast number of different functional groups.
- Long accused of being a latecomer to the electric vehicle game, Toyota has been busy lately telling the world how it's going to reinvent the way it produces cars in order to become an EV powerhouse.
- In a fume hood, a researcher used 5 grams of LAH to conduct a reduction reaction of a synthetic compound dissolved in mL of tetrahydrofuran THF.
CSI: Your trusted distributor of high quality chemical raw materials and laboratory equipment. This solution is a strong, versatile, and powerful reducing agent that can reduce a variety of functional groups in organic chemistry.
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