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Aluminum chloride hexahydrate is a chemical compound composed of aluminum and chlorine ions, with each unit bound to six water molecules. It is a water-soluble compound that typically appears as a clear or white, crystalline solid.

7784-13-6

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7784-13-6 Usage

Uses

Used in Skincare Products:
Aluminum chloride hexahydrate is used as an antiperspirant and astringent for its ability to reduce sweat and control body odor in various skincare formulations.
Used in Medical Treatments:
In the medical field, aluminum chloride hexahydrate is used as a treatment for hyperhidrosis, a condition characterized by excessive sweating, due to its effectiveness in managing perspiration.
Used in Surgical Procedures:
Aluminum chloride hexahydrate is utilized as an antiseptic in minor surgical procedures, providing a sterile environment and reducing the risk of infection.
Used in Industrial Applications:
Although not explicitly mentioned in the provided materials, aluminum chloride hexahydrate can also be used in various industrial applications such as water treatment, paper manufacturing, and dyeing processes, owing to its properties as a flocculant, deodorizer, and mordant.

Check Digit Verification of cas no

The CAS Registry Mumber 7784-13-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,8 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7784-13:
(6*7)+(5*7)+(4*8)+(3*4)+(2*1)+(1*3)=126
126 % 10 = 6
So 7784-13-6 is a valid CAS Registry Number.
InChI:InChI=1/Al.ClH.6H2O/h;1H;6*1H2/q+3;;;;;;;/p-1

7784-13-6 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (10622)  Aluminum chloride hexahydrate, Puratronic?, 99.9995% (metals basis)   

  • 7784-13-6

  • 5g

  • 330.0CNY

  • Detail
  • Alfa Aesar

  • (10622)  Aluminum chloride hexahydrate, Puratronic?, 99.9995% (metals basis)   

  • 7784-13-6

  • 50g

  • 821.0CNY

  • Detail
  • Alfa Aesar

  • (10622)  Aluminum chloride hexahydrate, Puratronic?, 99.9995% (metals basis)   

  • 7784-13-6

  • 250g

  • 3215.0CNY

  • Detail
  • Alfa Aesar

  • (10622)  Aluminum chloride hexahydrate, Puratronic?, 99.9995% (metals basis)   

  • 7784-13-6

  • 1kg

  • 7663.0CNY

  • Detail
  • Alfa Aesar

  • (A14437)  Aluminum chloride hexahydrate, 99%   

  • 7784-13-6

  • 250g

  • 315.0CNY

  • Detail
  • Alfa Aesar

  • (A14437)  Aluminum chloride hexahydrate, 99%   

  • 7784-13-6

  • 1000g

  • 1006.0CNY

  • Detail
  • Alfa Aesar

  • (A14437)  Aluminum chloride hexahydrate, 99%   

  • 7784-13-6

  • 5000g

  • 2721.0CNY

  • Detail
  • Alfa Aesar

  • (12297)  Aluminum chloride hexahydrate, Reagent Grade   

  • 7784-13-6

  • 500g

  • 509.0CNY

  • Detail
  • Alfa Aesar

  • (12297)  Aluminum chloride hexahydrate, Reagent Grade   

  • 7784-13-6

  • 2kg

  • 1527.0CNY

  • Detail
  • Sigma-Aldrich

  • (A0718)  Aluminumchloridehexahydrate  meets EP, BP, USP testing specifications

  • 7784-13-6

  • A0718-500G

  • 1,427.40CNY

  • Detail
  • Sigma-Aldrich

  • (A0718)  Aluminumchloridehexahydrate  meets EP, BP, USP testing specifications

  • 7784-13-6

  • A0718-1KG

  • 2,000.70CNY

  • Detail
  • Sigma-Aldrich

  • (A0718)  Aluminumchloridehexahydrate  meets EP, BP, USP testing specifications

  • 7784-13-6

  • A0718-2.5KG

  • 4,667.13CNY

  • Detail

7784-13-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name aluminium trichloride hexahydrate

1.2 Other means of identification

Product number -
Other names Aluminum chloride crystal

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7784-13-6 SDS

7784-13-6Relevant academic research and scientific papers

Regioselective Synthesis of 1,5-Disubstituted 1,2,3-Triazoles by Reusable AlCl3 Immobilized on γ-Al2O3

Nanjundaswamy, Hemmaragala M.,Abrahamse, Heidi

supporting information, p. 967 - 974 (2015/03/30)

(Chemical Equation Presented) There is rapidly growing interest in the synthesis and use of substituted 1,2,3-triazoles. We report an easy and interesting procedure that demonstrates the effectiveness of surface-modified γ-Al2O3, which is reusable, efficient, catalytic, safe, and environmentally acceptable for the regioselective synthesis of 1,5-disubstituted-1,2,3-triazoles via [3 + 2] cycloaddition of phenyl and benzyl azides with a series of aryl nitroolefins in good yields. No adverse effect on substituents such as nitro, cyano, hydroxy, ether linkage, and halogens was observed. The catalyst could easily be recycled and was reused for nine runs without losing its activity.

Application of reduced graphene oxide and carbon nanotube modified electrodes for measuring the enzymatic activity of alcohol dehydrogenase

Wang, Xianlong,Li, Li,Wang, Yanping,Xu, Chongzheng,Zhao, Bo,Yang, Xiaodi

, p. 2195 - 2200 (2013/06/26)

An electrochemical method was developed to measure the enzymatic activity of alcohol dehydrogenase (ADH) by monitoring the amount of reduced nicotinamide adenine dinucleotide (NADH) generated in the catalysed oxidation of ethanol by ADH. The concentration

Compositions of zirconium chloride complex and its method of manufacture

-

Page/Page column 2, (2010/11/24)

The invention discloses a process for preparing highly active aluminum zirconium tetrochlorohydrate glycine powder by forming aluminum chloride glycine and zirconium chloride glycine solution individually, and then blending such aluminum chloride glycine and zirconium chloride glycine together to form aluminum zirconium tetrochlorohydrate glycine.

Intermediates useful for the preparation of antihistaminic piperidine derivatives

-

Page column, (2010/01/30)

The present invention is related to a novel intermediates and processes which are useful in the preparation of certain antihistaminic piperidine derivatives of the formula whereinW represents —C(=O)— or —CH(OH)—;R1 represents hydrogen or hydroxy;R2 represents hydrogen;R1 and R2 taken together form a second bond between the carbon atoms bearing R1 and R2;n is an integer of from 1 to 5;m is an integer 0 or 1;R3 is —COOH or —COOalkyl wherein the alkyl moiety has from 1 to 6 carbon atoms and is straight or branched each of A is hydrogen or hydroxy; and pharmaceutically acceptable salts and individual optical isomers thereof,with the proviso that where R1 and R2 are taken together to form a second bond between the carbon atoms bearing R1 and R2 or where R1 represented hydroxy, m is an integer 0.

Pentaerythritol derivative

-

, (2008/06/13)

Complexes of pentaerythritol derivatives such as sulfuric acid ester of pentaerythritol or dipentaerythritol with a basic polyaluminum chloride and process for preparing the same are disclosed. The complex is novel and has a good anti-pepsin activity and therefore it is useful as an anti-ulcer agent.The complex is prepared by reacting pentaerythritol or dipentaerythritol with a sulfating agent and then reacting the resulting sulfate with a basic polyaluminum chloride.

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