Lithium Aluminum Hydride CAS 16853-85-3


Free Sample Lithium Aluminum Hydride CAS 16853-85-3
- Appearance:Powder
- Purity:99.8%
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Name: Lithium Aluminum Hydride
CAS: 16853-85-3
MOQ: 1KG
Directory Guidance on Lithium Aluminum Hydride
Chemical Structure
Basic Info:
Melting point | 125 °C (dec.)(lit.) |
Boiling point | 0°C |
bulk density | 400kg/m3 |
density | 0.97 g/mL at 20 °C |
Fp | 99 °F |
storage temp. | Store below +30°C. |
Product Introduction:
Lithium Aluminum Hydride (LiAlH₄) is an inorganic compound composed of lithium, aluminum and hydrogen elements, with a molecular formula of LiAlH₄ and a molecular weight of 37.95. It usually appears as a white or gray crystalline powder with strong hygroscopicity. After long-term storage, it may appear gray due to impurities or decomposition products. The compound will decompose at 125°C to produce lithium hydride (LiH), metallic aluminum (Al) and release hydrogen. Therefore, it must be strictly isolated from air and moisture during storage and use, and is usually operated under nitrogen or argon protection. The density of Lithium Aluminum Hydride is 0.917 g/cm³. It is easily soluble in ether solvents such as ether and tetrahydrofuran (THF), but it will react violently with protic solvents such as water and alcohols, and may even cause combustion or explosion, so it needs to be handled with caution.
The discovery of Lithium Aluminum Hydride can be traced back to the mid-20th century. In 1947, American chemists Schlesinger, Bond and Finholt successfully synthesized the substance for the first time by reacting lithium hydride with anhydrous aluminum chloride in ether. This method is called Schlesinger reaction. Since then, its synthesis process has been gradually optimized, such as using high-pressure synthesis method to directly react lithium, aluminum and hydrogen, or preparing from sodium aluminum hydride by double decomposition reaction. From the 1950s to the 1970s, with the rapid development of organic chemistry, it became a key reagent in laboratories and industries due to its excellent reducing ability. China began to study metal hydrides in the late 1950s and made important progress in the synthesis and application of Lithium Aluminum Hydride, especially in the military and civilian fields.
From the perspective of chemical properties, the core characteristic of Lithium Aluminum Hydride lies in its strong reducing ability. The four hydrogen atoms in its molecule can act as negative hydrogen ion (H⁻) donors, and can reduce a variety of functional groups (such as carbonyl, ester, amide, nitrile, etc.) to corresponding alcohols, amines or hydrocarbon compounds. For example, aldehydes and ketones are reduced to primary and secondary alcohols, esters can be completely reduced to two primary alcohols, and carboxylic acids are directly converted to primary alcohols. In addition, Lithium Aluminum Hydride can also participate in hydroalumination reactions, forming Al-C bond intermediates with olefins or alkynes, and further reacting with other reagents to form complex products. It is worth noting that its reduction selectivity can be adjusted by adding Lewis acids (such as AlCl₃), for example, converting α,β-unsaturated esters into allyl alcohols instead of fully saturated products.
Although Lithium Aluminum Hydride is highly chemically active, its danger cannot be ignored. It is highly flammable in both solid and solution states, and may cause violent exothermic reactions when in contact with water or moisture, producing hydrogen and causing explosion risks. Protective equipment must be strictly worn during operation and carried out in an inert gas environment. Do not use water or carbon dioxide when extinguishing a fire. Use dry graphite powder or a metal cover to isolate oxygen.
Nature and Specifications:
Item | Specification |
Product Name | Lithium Aluminum Hydride |
CAS No. | 16853-85-3 |
Appearance | Powder |
Shelf Life | 2 years |
Packing | As your requirements |
solubility | reacts with H2O, ethanol; seth, tetrahydrofuran |
form | tablets (~0.5 g each) |
Specific Gravity | 0.917 |
color | White to light gray |
Odor | Odorless solid |
Product service:
- Certificate Of Analysis (COA)
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- Route of synthesis (ROS)
- Method of Aanlysis (MOA)
- Nuclear Magnetic Resonance (NMR)
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Lithium Aluminum Hydride (LAH) has long been recognized for its use in organic synthesis, providing a versatile method to build complex molecular frameworks. Carbonyl compounds such as aldehydes, ketones, esters and carboxylic acids can be reduced to their respective alcohols via this technology, making it one of the key steps needed for drug intermediate synthesis, fragrance production and polymer materials production. Reduced amides and nitrile compounds can produce primary or secondary amines, while reduced amides produce primary or secondary amines; both reactions play a key role in synthesizing antidepressants, antibiotics, and anti-tumor drugs. Furthermore, Lithium Aluminum Hydride’s ring-opening reduction of epoxy compounds yields diol products used in polyether or surfactant production.
Lithium Aluminum Hydride has long been utilized by the pharmaceutical industry. Chemical reduction reactions are widely employed as an effective way of synthesizing active pharmaceutical ingredients, including chiral alcohols and amines, but can also serve as an antacid, neutralizing gastric acidity or producing compounds with anti-inflammatory or analgesic effects via reduction reactions. Lithium Aluminum Hydride excels at deprotection reactions, quickly creating molecules containing hydroxyl or amino groups to facilitate biological activities of drugs. Furthermore, this compound can selectively remove ester and amide protecting groups for multi-step synthesis to complete multi-step syntheses efficiently.
Lithium Aluminum Hydride has an exceptional place in energy and materials science, due to its high hydrogen content (about 10.6 weight percent). As one of several hydrogen storage materials with this characteristic, it releases hydrogen through thermal decomposition in a controlled fashion, making it suitable for fuel cells or hydrogen energy storage systems. Although its current cost may be high, its energy density and cycle stability far surpass traditional lead-acid batteries, especially when driving long distances such as electric ships. Furthermore, due to its conductive properties Lithium Aluminum Hydride makes useful addition to electronic materials, as an additive improving their performance such as improving polymeric performance conductivelyssium Aluminium Hydride can play a critical role.
Lithium Aluminum Hydride is often employed in the chemical industry to reduce halogenated hydrocarbons. Iodinated and bromoalkanes, for instance, can be converted using an SN2 mechanism which makes this process particularly efficient when dealing with primary halides. When applied to substrates containing oxygen functional groups (such as ortho acid derivatives) Lithium Aluminum Hydride can induce the formation of acetals which make this substance invaluable in fine chemical synthesis.
Lithium Aluminum Hydride has many uses; however, its limitations should also be kept in mind. Its strong reducing property can cause side reactions such as over-reduction or functional group interference, so to optimize reaction conditions or use sodium borohydride instead. Unreacted reagents need to be slowly quenched during post-treatment using either acetic acid or water to avoid violent exotherm.
The core competitiveness of Lithium Aluminum Hydride is first reflected in its irreplaceable reduction ability. Compared with other metal hydrides (such as sodium borohydride), its reduction range is wider and can act on highly stable functional groups such as carboxylic acids, esters, and amides, while sodium borohydride usually only reduces simple carbonyl compounds such as aldehydes and ketones.
Secondly, the controllability of the reaction of Lithium Aluminum Hydride is one of its technical advantages. Selective reduction can be achieved by adjusting the reaction conditions (such as temperature, solvent, additives). For example, the aluminum alkane (AlH₃) generated by mixing with aluminum trichloride has a weak reduction ability and can reduce α,β-unsaturated esters to allyl alcohol while retaining double bonds, avoiding excessive hydrogenation. This flexibility enables it to adapt to diverse synthesis needs in fine chemicals.
In industrial production, the large-scale preparation technology of Lithium Aluminum Hydride is becoming more and more mature. The yield of the early Schlesinger reaction has reached 86%, and the subsequent high-pressure synthesis method has further improved the efficiency. China has achieved industrial production since the 1990s, and has reduced costs through process innovation to promote its popularization in the military and civilian fields. The current commercialized Lithium Aluminum Hydride is supplied in the form of solid powder or ether solution, and the concentration is usually 0.5~1 mol/L, which is convenient for precise feeding and reaction control.
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chemicalbook-Lithium Aluminum Hydride
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