Lithium aluminum hydride solution [16853-85-3]
Referencia sc-228414A
embalaje : 1L
Marca : Santa Cruz Biotechnology
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Lithium aluminum hydride solution (CAS 16853-85-3)
Application(s):
Lithium aluminum hydride solution is a reducing reagent
Numéro CAS:
16853-85-3
Masse Moléculaire:
37.95
Formule Moléculaire:
LiAlH4
Information supplémentaire:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
Pour la Recherche Uniquement. Non conforme pour le Diagnostic ou pour une Utilisation Thérapeutique.
Available in US only.
Available in US only.
* Consulter le Certificat d'Analyses pour les données spécifiques à un lot (incluant la teneur en eau).
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Description
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SDS & Certificat d’Analyses
Lithium aluminum hydride solution is a powerful reducing agent may be used in organic synthesis. It functions by donating hydride ions to various organic compounds, leading to the reduction of functional groups such as carbonyl, carboxylic acids, and esters. Lithium aluminum hydride′s mechanism of action involves the transfer of hydride ions to the electrophilic carbon of the targeted functional group, resulting in the formation of alcohols or hydrocarbons. The hydride ions from the solution act as nucleophiles, attacking the electrophilic carbon and initiating the reduction reaction. This process is highly effective in the synthesis of a wide range of organic compounds, making lithium aluminum hydride a useful tool in research and development applications. Its ability to selectively reduce specific functional groups without affecting others makes it useful in the production of various organic molecules.
Lithium aluminum hydride solution (CAS 16853-85-3) Références:
- Stereospecific reduction of phosphine oxides to phosphines by the use of a methylation reagent and lithium aluminum hydride. | Imamoto, T., et al. 2001. Org Lett. 3: 87-90. PMID: 11429879
- A theoretical study of the reaction of lithium aluminum hydride with formaldehyde and cyclohexanone. | Luibrand, RT., et al. 2001. J Org Chem. 66: 7254-62. PMID: 11681935
- Regeneration of lithium aluminum hydride. | Graetz, J., et al. 2008. J Am Chem Soc. 130: 17790-4. PMID: 19053465
- Reduction of venom alkaloids in Solenopsis richteriSolenopsis invicta hybrid: an attempt to identify new alkaloidal components. | Chen, L., et al. 2010. J Agric Food Chem. 58: 11534-42. PMID: 20964344
- Methylated polyamines as research tools. | Khomutov, AR., et al. 2011. Methods Mol Biol. 720: 449-61. PMID: 21318892
- Buckyball-, carbon nanotube-, graphite-, and graphene-enhanced dehydrogenation of lithium aluminum hydride. | Hsu, CP., et al. 2013. Chem Commun (Camb). 49: 8845-7. PMID: 23958824
- Investigation on the synthesis of 25-hydroxycholesterol. | Zhao, Q., et al. 2014. Steroids. 85: 1-5. PMID: 24582707
- Practical Synthesis of the Bicyclic Darunavir Side Chain: (3R,3aS,6aR)-Hexahydrofuro[2,3-b]furan-3-ol from Monopotassium Isocitrate. | Moore, GL., et al. 2017. Org Process Res Dev. 21: 98-106. PMID: 28539755
- Axially chiral hemiaminals from nonracemic alpha -amino acid derivatives (thiohydantoins): Synthesis and isomer identification. | Sarigul Ozbek, S. and Dogan, I. 2020. Chirality. 32: 1299-1310. PMID: 32770589
- Formaldehyde-free self-polymerization of lignin-derived monomers for synthesis of renewable phenolic resin. | Yang, W., et al. 2021. Int J Biol Macromol. 166: 1312-1319. PMID: 33161075
- Green synthesis of graphite from CO2 without graphitization process of amorphous carbon. | Liang, C., et al. 2021. Nat Commun. 12: 119. PMID: 33402678
- Nucleophilic transformations of azido-containing carbonyl compounds via protection of the azido group. | Aimi, T., et al. 2021. Chem Commun (Camb). 57: 6062-6065. PMID: 34036976
- A new zeolitic lithium aluminum imidazolate framework. | Jiang, G., et al. 2021. Dalton Trans. 50: 7933-7937. PMID: 34075989
- General Method to Increase Carboxylic Acid Content on Nanodiamonds. | Shenoy, G., et al. 2022. Molecules. 27: PMID: 35164002
- Inverse Electron-Demand Aza-Diels-Alder Reaction of alpha , beta -Unsaturated Thioesters with In Situ-Generated 1,2-Diaza-1,3-dienes for the Synthesis of 1,3,4-Thiadiazines. | Shen, LW., et al. 2022. J Org Chem. 87: 4232-4240. PMID: 35212520
Formulation :
2.0 M in THF
État Physique :
Liquid
Stockage :
Store at 4° C
Point d'Ébullition :
66° C
Densité :
0.906 g/cm3 at 25° C
Pour la Recherche Uniquement. Non conforme pour le Diagnostic ou pour une Utilisation Thérapeutique.
Available in US only.
Available in US only.
Transport :
Not available for sale outside of the United States.
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Lithium aluminum hydride solution | CAS 16853-85-3 SAMPLE Certificate of AnalysisCERTIFICAT D'ANALYSE
Numéro de catalogue
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SAMPLE Certificate of Analysis (COA)
Catalog Number:sc-228414
Lot Number:SAMPLE
Product Name:Lithium aluminum hydride solution
Molecular Formula:LiAlH4
Molecular Weight:37.95
Test | Specification | Results |
---|---|---|
Appearance | Clear to slightly hazy colorless liquid | Clear colorless liquid |
Hydrogen Evolution | 1.90 - 2.20 M | 2.11 M |
TEST CONDITIONS
Exp. Date: 8/15/2024
Informations pour la commande
Nom du produit | Ref. Catalogue | COND. | Prix HT | QTÉ | Favoris | |
Lithium aluminum hydride solution, 100 ml | sc-228414 | 100 ml | .00 | |||
Lithium aluminum hydride solution, 1 L | sc-228414A | 1 L | .00 |