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Aluminum Chloride

Q: What are the common industrial and laboratory applications of Aluminum Chloride?

Aluminum chloride has a wide range of applications, including: - As a catalyst in organic synthesis reactions - As a dehydrating agent - In the production of other aluminum compounds - In water treatment processes - In textile dyeing and finishing - In antiperspirant and deodorant formulations - As a starting material for the synthesis of other aluminum salts

Aluminum chloride is an inorganic compound with the chemical formula AlCl3.
It is a white, crystalline solid that is soluble in water and organic solvents.
Aluminum chloride has a wide range of industrial and laboratory applications, including as a catalyst in organic synthesis, a dehydrating agent, and a component in antiperspirants.
It is also used in water treatment, textile dyeing, and the production of other aluminum compounds.
Researchers studying aluminum chloride can leverage AI-driven platforms like PubCompare.ai to easily locate the most accurate and reproducible experimental protocols from scientific literature, preprints, and patents.
This can help streamline the research process, improve experimental accuracy and efficacy, and identify the best products for your aluminum chloroide studies.

Most cited protocols related to «Aluminum Chloride»

Quantification of Flavonoids in Plants

The aluminum chloride colorimetric method was used for the determination of the total flavonoid content of the sample [21 –24 ]. For total flavonoid determination, quercetin was used to make the standard calibration curve. Stock quercetin solution was prepared by dissolving 5.0 mg quercetin in 1.0 mL methanol, then the standard solutions of quercetin were prepared by serial dilutions using methanol (5–200 μg/mL). An amount of 0.6 mL diluted standard quercetin solutions or extracts was separately mixed with 0.6 mL of 2% aluminum chloride. After mixing, the solution was incubated for 60 min at room temperature. The absorbance of the reaction mixtures was measured against blank at 420 nm wavelength with a Varian UV-Vis spectrophotometer (Cary 50 Bio UV-Vis Spectrophotometer, Varian). The concentration of total flavonoid content in the test samples was calculated from the calibration plot (Y = 0.0162x + 0.0044, R² = 0.999) and expressed as mg quercetin equivalent (QE)/g of dried plant material. All the determinations were carried out in triplicate.

Chandra S., Khan S., Avula B., Lata H., Yang M.H., ElSohly M.A, & Khan I.A. (2014). Assessment of Total Phenolic and Flavonoid Content, Antioxidant Properties, and Yield of Aeroponically and Conventionally Grown Leafy Vegetables and Fruit Crops: A Comparative Study. Evidence-based Complementary and Alternative Medicine : eCAM, 2014, 253875.

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Publication 2014

Aluminum Chloride Colorimetry Flavonoids Methanol Plants Quercetin Technique, Dilution

Determination of Total Flavonoids

Total flavonoid content was determined following a method by Park et al (2008) [28 (link)]. In a 10 ml test tube, 0.3 ml of extracts, 3.4 ml of 30% methanol, 0.15 ml of NaNO₂ (0.5 M) and 0.15 ml of AlCl₃.6H₂O (0.3 M) were mixed. After 5 min, 1 ml of NaOH (1 M) was added. The solution was mixed well and the absorbance was measured against the reagent blank at 506 nm. The standard curve for total flavonoids was made using rutin standard solution (0 to 100 mg/l) under the same procedure as earlier described. The total flavonoids were expressed as milligrams of rutin equivalents per g of dried fraction.

Saeed N., Khan M.R, & Shabbir M. (2012). Antioxidant activity, total phenolic and total flavonoid contents of whole plant extracts Torilis leptophylla L. BMC Complementary and Alternative Medicine, 12, 221.

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Publication 2012

Aluminum Chloride Flavonoids Methanol Rutin

Flavonoid Content Quantification Method

The flavonoid contents of individual extracts were measured as per the Dowd method [46 (link)]. An aliquot of 1 mL of extract solution (25–200 µg/mL) or quercetin (25–200 µg/mL) were mixed with 0.2 mL of 10% (w/v) AlCl₃ solution in methanol, 0.2 mL (1 M) potassium acetate and 5.6 mL distilled water. The mixture was incubated for 30 min at room temperature followed with the measurement of absorbance at 415 nm against the blank. The outcome data were expressed as mg/g of quercetin equivalents in milligrams per gram (mg QE/g) of dry extract.

Aryal S., Baniya M.K., Danekhu K., Kunwar P., Gurung R, & Koirala N. (2019). Total Phenolic Content, Flavonoid Content and Antioxidant Potential of Wild Vegetables from Western Nepal. Plants, 8(4), 96.

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Publication 2019

Aluminum Chloride Flavonoids Methanol Potassium Acetate Quercetin

Quantifying Flavonoids in L. aromatica

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Publication 2013

Aluminum Chloride Colorimetry Flavonoids Methanol Potassium Acetate Quercetin

Comprehensive Phytochemical Analysis of Extract

The total phenolic content was determined by employing the methods given in the literature (Slinkard and Singleton, 1977 (link)) with some modification. Sample solution (1 mg/mL; 0.25 mL) was mixed with diluted Folin–Ciocalteu reagent (1 mL, 1:9, v/v) and shaken vigorously. After 3 min, Na₂CO₃ solution (0.75 mL, 1%) was added and the sample absorbance was read at 760 nm after a 2 h incubation at room temperature. The total phenolic content was expressed as milligrams of gallic acid equivalents (mg GAE/g extract) (Vlase et al., 2014 ).
The total flavonoids content was determined using AlCl₃ method (Zengin et al., 2014 (link)). Briefly, sample solution (1 mg/mL; 1 mL) was mixed with the same volume of aluminum trichloride (2%) in methanol. Similarly, a blank was prepared by adding sample solution (1 mL) to methanol (1 mL) without AlCl₃. The sample and blank absorbances were read at 415 nm after a 10 min incubation at room temperature. The absorbance of the blank was subtracted from that of the sample. Rutin was used as a reference standard and the total flavonoid content was expressed as milligrams of rutin equivalents (mg RE/g extract) (Mocan et al., 2015 (link)).
The total saponins content of the extract was determined by the vanillin-sulfuric acid method (Aktumsek et al., 2013 (link)). Sample solution (1 mg/mL; 0.25 mL) was mixed with vanillin (0.25 mL, 8%) and sulfuric acid (2 mL, 72%). The mixture was incubated for 10 min at 60°C. Then the mixture was cooled for another 15 min, followed by the sample absorbance measurement at 538 nm. The total saponin content was expressed as milligrams of quillaja equivalents (mg QAE/g extract).
The total triterpenoids content of the extracts was determined according to Zhang et al. (2010) (link) method with some modifications. Briefly, sample solution (1 mg/mL; 500 μL) was mixed with the vanillin–glacial acetic acid (5%, w/v, 0.5 mL) and 1 mL of perchloric acid. The mixture was incubated at 60°C for 10 min, cooled in an ice water bath for 15 min and then 5 mL glacial acetic acid was added and mixed well. After 6 min, the absorbance was read at 538 nm. Oleanolic acid was used as a reference standard and the content of total triterpenoids was expressed as oleanolic acid equivalents (mg OAE/g extract) through a calibration curve with oleanolic acid.
HPLC-PDA analyses were performed on a Waters liquid chromatograph equipped with a model 600 solvent pump and a 2996 photodiode array detector, and Empower v.2 Software (Waters Spa, Milford, MA, United States) was used for acquisition of data. A C18 reversed-phase packing column (Prodigy ODS (3), 4.6 × 150 mm, 5 μm; Phemomenex, Torrance, CA, United States) was used for the separation and the column was thermostated at 30 ± 1°C using a Jetstream2 Plus column oven. The injection volume was 20 μL. The mobile phase was directly on-line degassed by using Biotech DEGASi, mod. Compact (LabService, Anzola dell’Emilia, Italy). Gradient elution was performed using the mobile phase water-acetonitrile (93:7, v/v, 3% acetic acid) (Zengin et al., 2016 (link)). The UV/Vis acquisition wavelength was set in the range of 200–500 nm. The quantitative analyses were achieved at maximum wavelength for each compound.

Uysal S., Zengin G., Locatelli M., Bahadori M.B., Mocan A., Bellagamba G., De Luca E., Mollica A, & Aktumsek A. (2017). Cytotoxic and Enzyme Inhibitory Potential of Two Potentilla species (P. speciosa L. and P. reptans Willd.) and Their Chemical Composition. Frontiers in Pharmacology, 8, 290.

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Publication 2017

Acetic Acid acetonitrile Aluminum Chloride Bath Flavonoids folin Gallic Acid High-Performance Liquid Chromatographies Ice Liquid Chromatography Methanol Oleanolic Acid Perchloric Acid Prodigy Quillaja Rutin Saponin Saponins Solvents sulfuric acid Triterpenes vanillin

Most recents protocols related to «Aluminum Chloride»

Synthesis and Surface Modification of Hydrotalcite Particles

Not available on PMC !

Example 1

In a 2 L stainless steel container, 730 g of aluminum hydroxide powder (commercially available from KANTO CHEMICAL CO., INC., Cica special grade) were added into 1110 mL of 48% sodium hydroxide solution (commercially available from KANTO CHEMICAL CO., INC., Cica special grade), and they were stirred at 124° C. for 1 hour to give a sodium aluminate solution (First Step).

After the sodium aluminate solution was cooled to 80° C., ion exchange water was added into the sodium aluminate solution to achieve a total amount of 1500 mL.

After 96 mL of the sodium aluminate solution were separated into a 1 L stainless steel container, pure water was added into the solution to achieve a total amount of 730 mL (concentration of the sodium aluminate solution: 0.8 mol/L). The solution was stirred with keeping a temperature thereof at 25° C., and the solution was aerated with carbon dioxide in an aeration amount of 0.7 L/min. for 60 minutes to give adjusted aluminum hydroxide slurry (low-crystallinity aluminum compound=pseudo-boehmite) (Second Step).

Separately, 49.5 g of magnesium oxide powder (commercially available from KANTO CHEMICAL CO., INC., special grade) were added to 327 mL of pure water, and they were stirred for 1 hour to give magnesium oxide slurry.

In a 1.5 L stainless steel container, the magnesium oxide slurry and the adjusted aluminum hydroxide slurry were added into 257 mL of pure water, and they were stirred at 55° C. for 90 minutes to cause a first-order reaction. As a result, a reactant containing hydrotalcite nuclear particles was prepared (Third Step).

Then, pure water was added to the reactant to give a solution in a total amount of 1 L. The solution was put into a 2 L autoclave, and a hydrothermal synthesis was performed at 160° C. for 7 hours. As a result, hydrotalcite particles slurry was synthesized (Fourth Step).

To the hydrotalcite particles slurry were added 4.3 g of stearic acid (3 parts by mass with respect to 100 parts by mass of hydrotalcite particles) with keeping a temperature of the hydrotalcite particles slurry at 95° C. to perform a surface treatment on particles (Fifth Step). After the hydrotalcite particles slurry of which particles were surface treated was filtered and washed, a drying treatment was performed at 100° C. to give solid products of hydrotalcite particles. The produced hydrotalcite particles were subjected to an elemental analysis, resulting in that Mg/Al (molar ratio)=2.1.

In accordance with a method of Example 1 described in Japanese Laid-Open Patent Publication No. 2003-048712, hydrotalcite particles were synthesized.

In 150 g/L of NaOH solution in an amount of 3 L were dissolved 90 g of metal aluminum to give a solution. After 399 g of MgO were added to the solution, 174 g of Na₂CO₃were added thereto and they were reacted with each other for 6 hours with stirring at 95° C. As a result, hydrotalcite particles slurry was synthesized.

To the hydrotalcite particles slurry were added 30 g of stearic acid (3 parts by mass with respect to 100 parts by mass of hydrotalcite particles) with keeping a temperature of the hydrotalcite particles slurry at 95° C. to perform a surface treatment on particles. After the hydrotalcite particles slurry of which particles were surface treated was cooled, filtered and washed to give solid matters, a drying treatment was performed on the solid matters at 100° C. to give solid products of hydrotalcite particles.

Example 2

After the sodium aluminate solution was cooled to 80° C., ion exchange water was added into the sodium aluminate solution to achieve a total amount of 1500 mL.

After 96 mL of the sodium aluminate solution were separated into a 1 L stainless steel container, pure water was added into the solution to achieve a total amount of 730 mL (concentration of the sodium aluminate solution: 0.8 mol/L). The solution was stirred with keeping a temperature thereof at 30° C., and the solution was aerated with carbon dioxide in an aeration amount of 0.7 L/min. for 90 minutes to give adjusted aluminum hydroxide slurry (low-crystallinity aluminum compound=pseudo-boehmite) (Second Step).

Solid products of hydrotalcite particles were produced in a same manner as in Comparative Example 1 except that reaction conditions of 95° C. and 6 hours for synthesis of the hydrotalcite particles slurry in Comparative Example 1 were changed to hydrothermal reaction conditions of 170° C. and 6 hours.

Example 3

After the sodium aluminate solution was cooled to 80° C., ion exchange water was added into the sodium aluminate solution to achieve a total amount of 1500 mL.

After 96 mL of the sodium aluminate solution were separated into a 1 L stainless steel container, pure water was added into the solution to achieve a total amount of 730 mL (concentration of the sodium aluminate solution: 0.8 mol/L). The solution was stirred with keeping a temperature thereof at 60° C., and the solution was aerated with carbon dioxide in an aeration amount of 0.7 L/min. for 60 minutes to give adjusted aluminum hydroxide slurry (low-crystallinity aluminum compound=pseudo-boehmite) (Second Step).

In accordance with a method of Example 1 described in Japanese Laid-Open Patent Publication No. 2013-103854, hydrotalcite particles were synthesized.

Into a 5 L container were added 447.3 g of magnesium hydroxide (d50=4.0 μm) and 299.2 g of aluminum hydroxide (d50=8.0 μm), and water was added thereto to achieve a total amount of 3 L. They were stirred for 10 minutes to prepare slurry. The slurry had physical properties of d50=10 μm and d90=75 μm. Then, the slurry was subjected to wet grinding for 18 minutes (residence time) by using Dinomill MULTILAB (wet grinding apparatus) with controlling a slurry temperature during grinding by using a cooling unit so as not to exceed 40° C. As a result, ground slurry had physical properties of d50=1.0 μm, d90=3.5 μm, and slurry viscosity=5000 cP. Then, sodium hydrogen carbonate was added to 2 L of the ground slurry such that an amount of the sodium hydrogen carbonate was ½ mole with respect to 1 mole of the magnesium hydroxide. Water was added thereto to achieve a total amount of 8 L, and they were stirred for 10 minutes to give slurry. Into an autoclave was put 3 L of the slurry, and a hydrothermal reaction was caused at 170° C. for 2 hours. As a result, hydrotalcite particles slurry was synthesized.

To the hydrotalcite particles slum were added 6.8 g of stearic acid (3 parts by mass with respect to 100 parts by mass of hydrotalcite particles) with keeping a temperature of the hydrotalcite particles slurry at 95° C. to perform a surface treatment on particles. After solids were filtered by filtration, the filtrated cake was washed with 9 L of ion exchange water at 35° C. The filtrated cake was further washed with 100 mL of ion exchange water, and a conductance of water used for washing was measured. As a result, the conductance of this water was 50 μS/sm (25° C.). The water-washed cake was dried at 100° C. for 24 hours and was ground to give solid products of hydrotalcite particles.

Example 5

After the sodium aluminate solution was cooled to 80° C., ion exchange water was added into the sodium aluminate solution to achieve a total amount of 1500 mL.

After 192 mL of the sodium aluminate solution were separated into a 1 L stainless steel container, pure water was added into the solution to achieve a total amount of 730 mL (concentration of the sodium aluminate solution: 1.6 mol/L). The solution was stirred with keeping a temperature thereof at 30° C., and the solution was aerated with carbon dioxide in an aeration amount of 0.7 L/min. for 90 minutes to give adjusted aluminum hydroxide slurry (low-crystallinity aluminum compound=pseudo-boehmite) (Second Step).

In accordance with a method of Example 1 described in Japanese Laid-Open Patent Publication No. H06-136179, hydrotalcite particles were synthesized.

To 1 L of water were added 39.17 g of sodium hydroxide and 11.16 g of sodium carbonate with stirring, and they were heated to 40° C. Then, to 500 mL of distilled water were added 61.28 g of magnesium chloride (19.7% as MgO), 37.33 g of aluminum chloride (20.5% as Al₂O₃), and 2.84 g of ammonium chloride (31.5% as NH₃) such that a molar ratio of Mg to Al, Mg/Al, was 2.0 and a molar ratio of NH₃to Al, NH₃/Al, was 0.35. As a result, an aqueous solution A was prepared. The aqueous solution A was gradually poured into a reaction system of the sodium hydroxide and the sodium carbonate. The reaction system after pouring had pH of 10.2. Moreover, a reaction of the reaction system was caused at 90° C. for about 20 hours with stirring to give hydrotalcite particles slurry.

To the hydrotalcite particles slurry were added 1.1 g of stearic acid, and a surface treatment was performed on particles with stirring to give a reacted suspension. The reacted suspension was subjected to filtration and water washing, and then the reacted suspension was subjected to drying at 70° C. The dried suspension was ground by a compact sample mill to give solid products of hydrotalcite particles.

US11873230B2. Hydrotalcite particles, method for producing hydrotalcite particles, resin stabilizer containing hydrotalcite particles, and resin composition containing hydrotalcite particles (2024-01-16). TODA KOGYO CORP. [JP], SAKAI CHEMICAL INDUSTRY CO., LTD. [JP]. Inventors: Koji Kakuya [JP], Atsuko Yasunaga [JP], Nobukatsu Shigi [JP].

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Patent 2024

A-A-1 antibiotic Aluminum Aluminum Chloride aluminum oxide hydroxide Anabolism Bicarbonate, Sodium Carbon dioxide Chloride, Ammonium Filtration hydrotalcite Hydroxide, Aluminum Ion Exchange Japanese Magnesium Chloride Magnesium Hydroxide Molar Oxide, Magnesium Physical Processes Powder Resins, Plant sodium aluminate sodium carbonate Sodium Hydroxide Stainless Steel stearic acid Suby's G solution Viscosity

Isomerization of para-cymene with AlCl3

Not available on PMC !

Example 1

A mixture of about 2 g of para-cymene and 0.1 g of anhydrous aluminum chloride was heated to 60° C. for 5 hours. At the end of 5 hours, the reaction mixture was quenched with water and the resulting organic layer was analyzed by GC and GCMS. The product showed a mixture of cymene isomers (67.6%), toluene (10.8%) and methyl di-isopropyl benzene isomers (20.8%). Para-cymene has a by of 177.10° C.; meta-cymene has a bp of 175.14° C.; and ortho-cymene has a bp of 178.15° C.

US11873277B2. Circular economic methods for fragrance ingredients (2024-01-16). International Flavors & Fragrances Inc. [US]. Inventors: Sunitha R. Tadepalli [US], Paul Daniel Jones [US], Geatesh K. Tampy [US], John P. Cherkauskas [US].

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Patent 2024

Aluminum Chloride Anhydrous Aluminum Chloride Cymene Gas Chromatography-Mass Spectrometry Isomerism Lewis Acids Toluene

Synthesis of Titanium-Aluminum-Vanadium Alloy

Not available on PMC !

Example 7

First, 120 g of a titanium-aluminum-vanadium chloride mixture was prepared, by mixing liquid titanium chloride (from Sigma Aldrich), aluminum chloride powder (from Strem Chemical) and liquid vanadium chloride (from Acros Organics). The mixture was stirred constantly to maintain a dispersion of the aluminum chloride.

Next, 140 g of sodium metal was heated to 250° C. in an Inconel vessel and stirred by a Cowles blade mixer at speeds ranging from 1000 rpm initially, to 2500 rpm as the reaction progressed. The chloride mixture was pumped into the reactor until 74 g had been added, over approximately 90 minutes. The reaction stopped when the vortex in the sodium could no longer be maintained.

The reactor vessel was then sealed and transferred to a furnace, brought to 825° C. and held at that temperature for approximately one hour before being allowed to cool.

The recovered product was then washed to remove the sodium chloride coating the metal powder, and the powder was dried in a vacuum oven at 100 C for 24 hours.

Analysis of the metal powder using ICPMS showed the product contained under 50 ppm iron and under 150 ppm total transition metals. The results demonstrate that the titanium powder falls within the purity limits as described in UNS No. R56400.

US11858046B2. Methods for producing metal powders (2024-01-02). Nanoscale Powders LLC [US]. Inventors: David Henderson [US], Andrew Matheson [US], Richard Van Lieshout [US], Donald Finnerty [US], John W. Koenitzer [US].

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Patent 2024

Aluminum Aluminum Chloride ARID1A protein, human Blood Vessel Chlorides Iron-50 Metals Powder Sodium Sodium Chloride Titanium Transition Elements Vacuum Vanadium

Synthesis of Titanium-Aluminum Metal Alloy

Not available on PMC !

Example 6

120 g of a 55% aluminum, 45% titanium powder (measured by metal content) was first prepared, by adding aluminum chloride powder (from Strem Chemical) to an aluminum-titanium chloride Ziegler Natta catalyst powder (also from Strem Chemical).

Next, 140 g of sodium metal was placed in an Inconel reactor and heated to 250° C. Over approximately 2 hours, 94 g of the titanium-aluminum chloride powder mix was pulse fed into the sodium, which was continuously stirred by a Cowles blade mixer at between 1600 and 2500 rpm. Powder addition continued until the mixer could no longer maintain a vortex in the sodium. At the end of the reaction the sodium temperature had increased to 292° C.

The Inconel reactor was then sealed, transferred to a furnace, and heated to 900° C. for 1 hour. After this step, the unreacted sodium was removed and the metal powder washed to remove its salt coating. Washing continued until the wash water conductivity fell below 2 microsiemens. Finally, the powder was dried in a vacuum over for 24 hours.

The titanium-aluminum metal thus produced was found by ICPMS analysis to contain below 1000 ppm iron and below 1500 ppm total transition metals.

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Patent 2024

Aluminum Aluminum Chloride Electric Conductivity Iron Metals Powder Pulse Rate Sodium Sodium Chloride Titanium Transition Elements Vacuum

Molten Salt Electrolyte Synthesis

Not available on PMC !

Example 1

A reference electrolyte used for the examples described below was produced according to the method described in patent specification EP 2 954 588 B1 (hereinafter referred to as [V4]). First, lithium chloride (LiCl) was dried under vacuum at 120° C. for three days. Aluminum particles (Al) were dried under vacuum for two days at 450° C. LiCl, aluminum chloride (AlCl₃) and Al were mixed together in an AlCl₃:LiCl:Al molar ratio of 1:1.06:0.35 in a glass bottle having an opening to allow gas to escape. This blend was thereafter heat-treated in stages to produce a molten salt. After cooling, the salt melt formed was filtered, then cooled to room temperature and finally SO₂was added until the desired molar ratio of SO₂to LiAlCl₄was formed. The reference electrolyte thus formed had the composition LiAlCl₄*x SO₂, wherein x is dependent on the amount of SO₂supplied.

US11876170B2. Rechargeable battery cell (2024-01-16). Innolith Technology AG [CH]. Inventors: Laurent Zinck [FR], Christian Pszolla [DE], Markus Borck [DE].

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Patent 2024

Aluminum Aluminum Chloride Chloride, Lithium Electrolytes Molar Sodium Chloride Vacuum

Top products related to «Aluminum Chloride»

Gallic acid by Merck Group

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Gallic acid is a naturally occurring organic compound that can be used as a laboratory reagent. It is a white to light tan crystalline solid with the chemical formula C6H2(OH)3COOH. Gallic acid is commonly used in various analytical and research applications.

Quercetin by Merck Group

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Quercetin is a natural compound found in various plants, including fruits and vegetables. It is a type of flavonoid with antioxidant properties. Quercetin is often used as a reference standard in analytical procedures and research applications.

Folin ciocalteu reagent by Merck Group

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The Folin-Ciocalteu reagent is a colorimetric reagent used for the quantitative determination of phenolic compounds. It is a mixture of phosphomolybdic and phosphotungstic acid complexes that undergo a color change when reduced by phenolic compounds.

2 2 diphenyl 1 picrylhydrazyl (dpph) by Merck Group

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DPPH is a chemical compound used as a free radical scavenger in various analytical techniques. It is commonly used to assess the antioxidant activity of substances. The core function of DPPH is to serve as a stable free radical that can be reduced, resulting in a color change that can be measured spectrophotometrically.

Aluminum chloride by Merck Group

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Aluminum chloride is a chemical compound with the formula AlCl3. It is a colorless crystalline solid that is soluble in water and organic solvents. Aluminum chloride is used as a catalyst in various chemical reactions and as a drying agent.

Sodium carbonate by Merck Group

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Sodium carbonate is a water-soluble inorganic compound with the chemical formula Na2CO3. It is a white, crystalline solid that is commonly used as a pH regulator, water softener, and cleaning agent in various industrial and laboratory applications.

Sodium hydroxide (naoh) by Merck Group

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Sodium hydroxide is a chemical compound with the formula NaOH. It is a white, odorless, crystalline solid that is highly soluble in water and is a strong base. It is commonly used in various laboratory applications as a reagent.

Methanol by Merck Group

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Methanol is a clear, colorless, and flammable liquid that is widely used in various industrial and laboratory applications. It serves as a solvent, fuel, and chemical intermediate. Methanol has a simple chemical formula of CH3OH and a boiling point of 64.7°C. It is a versatile compound that is widely used in the production of other chemicals, as well as in the fuel industry.

Ascorbic acid by Merck Group

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Ascorbic acid is a chemical compound commonly known as Vitamin C. It is a water-soluble vitamin that plays a role in various physiological processes. As a laboratory product, ascorbic acid is used as a reducing agent, antioxidant, and pH regulator in various applications.

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Catechin is a natural polyphenolic compound found in various plants, including green tea. It functions as an antioxidant, with the ability to scavenge free radicals and protect cells from oxidative stress.

What are the different forms or types of Aluminum Chloride?

Aluminum chloride (AlCl3) is available in several forms, including anhydrous (without water) and hydrated (with water) versions. The anhydrous form is a white, crystalline solid, while the hydrated forms can be in the form of hexahydrate (AlCl3·6H2O) or other hydration states. The different forms of aluminum chloride can have slightly varying properties and applications.

What are the common industrial and laboratory applications of Aluminum Chloride?

What are some potential challenges or considerations when working with Aluminum Chloride?

When handling and using aluminum chloride, there are a few important considerations: - Aluminum chloride is highly reactive and can be corrosive, so proper safety precautions are necessary when working with it. - The hydrated forms of aluminum chloride are hygroscopic, meaning they readily absorb moisture from the air, which can affect the purity and consistency of the material. - Aluminum chloride can sometimes produce hydrogen chloride gas, which is toxic, so proper ventilation is crucial. - Careful attention to stoichiometry and precise measurements are important when using aluminum chloride in chemical reactions, as the compound can be very reactive.

How can PubCompare.ai help with Aluminum Chloride research and optimization?

PubCompare.ai can be a valuable tool for researchers working with aluminum chloride in several ways: 1. The platform allows you to efficiently screen through protocol literature to identify the most accurate and reproducible experimental procedures related to aluminum chloride. 2. PubCompare.ai's AI-driven analysis can help pinpoint critical insights, such as identifying the most effective aluminum chloride protocols for your specific research goals and highlighting key differences in protocol effectiveness. 3. By leveraging the platform's AI comparisons, you can choose the best products and protocols to ensure high reproducibility and accuracy in your aluminum chloride experiments, streamlining your research process.

Are there any safety or handling precautions to consider when working with Aluminum Chloride?

Yes, there are several important safety and handling precautions to keep in mind when working with aluminum chloride: - Aluminum chloride is a corrosive substance, so proper personal protective equipment (PPE) such as gloves, goggles, and a lab coat should alawys be worn. - The compound can produce toxic hydrogen chloride gas, so work should be conducted in a well-ventilated area or fume hood. - Aluminum chloride is hygroscopic, meaning it readily absorbs moisture from the air, so it should be stored in airtight containers to maintain its purity and consistency. - Proper disposal methods for aluminum chloride waste must be followed, as it can be hazardous to the environment.

More about "Aluminum Chloride"

AlCl3, inorganic compound, water treatment, textile dyeing, organic synthesis, dehydrating agent, aluminum compounds, PubCompare.ai, gallic acid, quercetin, Folin-Ciocalteu reagent, DPPH, sodium carbonate, sodium hydroxide, methanol, ascorbic acid, catechin