10294-29-8

Basic information

• Product Name: Gold(I) chloride
• Synonyms: Aurouschloride;Gold monochloride;Gold(1+) chloride;Gold(I) chloride
• CAS NO: 10294-29-8
• Molecular Formula: AuCl
• Molecular Weight: 0
• EINECS: 233-655-8
• Mol File: 10294-29-8.mol
• Article Data: 16

Chemical Properties

• Melting Point: 289℃
• Appearance: /
• Density: 7.57 g/mL at 25 °C(lit.)
• Vapor Pressure: 33900mmHg at 25°C
• CAS DataBase Reference: Gold(I) chloride(CAS DataBase Reference)
• NIST Chemistry Reference: Gold(I) chloride(10294-29-8)
• EPA Substance Registry System: Gold(I) chloride(10294-29-8)

Safety Data

• Hazardous Substances Data: 10294-29-8(Hazardous Substances Data)

Usage

General Description

Gold(I) chloride, also known as aurous chloride, is a chemical compound with the formula AuCl. It is a yellow solid that is highly soluble in water and is commonly used as a precursor for the synthesis of other gold compounds. Gold(I) chloride is a key reagent in the production of gold nanoparticles and is often used in the electronics industry for creating conductive materials. It also has applications in the field of medicine, particularly in the treatment of certain types of cancers. Additionally, it has been studied for its potential use in catalysis and as a catalyst for various organic reactions. Overall, gold(I) chloride has a wide range of uses in different industries and research fields due to its unique properties and versatile applications.

InChI:InChI=1/Au.3ClH/h;3*1H/q+3;;;/p-3

Upstream product

• 7440-57-5 gold 
• 13453-07-1 gold(III) chloride 
• 7782-50-5 chlorine 
• 21792-06-3 arsenite 
• 74-86-2 acetylene 
• 50960-82-2 carbonylgold(I) chloride 
• 21563-00-8 gold(III) chloride 
• 75-15-0 carbon disulfide 
• 108-98-5 thiophenol 
• 1303-50-0 hydrogen tetrachloroaurate(III) tetrahydrate 

Downstream Products

• 76423-00-2 chloro(2-methyl-5-phenyl-1,2,4,3σ(2)-triazaphosphole)gold(I) 
• 10294-31-2 gold(I) iodide 
• 83846-07-5 N₃P₃(OC₆H₄(C₆H₅)2PAuCl)6 
• 1414687-13-0 tetra-tert-butylphthalocyanine gold(III) chloride 
• 1414687-19-6 gold(III) [18]tribenzo-pentaaza-triphyrin 
• 1346522-93-7 phthalocyanine gold(III) chloride 
• 1420831-83-9 [Ir(fac-bis[(2-diphenylphosphino)phenyl]phosphide)(AuCl)(COD)] 
• 1446342-19-3 C₅₇H₇₈AuClN₆Ni₂O₂PS₂⁽¹⁺⁾*ClO₄^(1-) 

Relevant articles and documents

New production of gold resinate

PROBLEM TO BE SOLVED: conventional gold resinate paste by improving the difficulty in firing temperature of 450 °C fired during low temperature of the mold has a sheet resistance which is suitable for forming a film of gold resinate paste to provide a novel method for manufacturing the metal resinate. SOLUTION: a metallic compound represented by general eq. (1) pH7.0-14.0 aq. 0 °C -100 ° C is adjusted to keep the temperature, this soln. mercaptocarboxylic acetic acid, 3-mercapto propionate, mercaptocarboxylic hydroxybutanoate 4-, 5-and 6-mercaptocarboxylic hydroxyhexanamide mercaptocarboxylic Pentaenoic acid selected from 1-15 min. mercaptocarboxylic acid is added to the reaction expressed by the general eq. (2) can be obtained in high yield of gold resinate Selected drawing: no

MANUFACTURING METHOD OF GOLD COMPOUND

PROBLEM TO BE SOLVED: To provide a gold compound having no cyan useful as a gold source for non-electrolytic and electrolytic plating liquid. SOLUTION: There is provided a gold compound represented by the general formula (1), which is a crystal obtained by suspending alkali metal salts such as sodium first gold compound chloride synthesized form chloroauric acid, alkali metal salt and an organic compound having a thiol group in an aqueous solution, then reacting them under a condition of pH of 7.0 to 13.5 and temperature of 10 to 90°C in a presence of inert gas such as argon gas or nitrogen gas, column purifying deposited crystal by alcohol after a reaction end. The gold compound is available as a gold source for non-electrolytic and electrolytic plating liquid having no cyan in a plating bath. (1), where R represents a monovalent alkyl group, an aryl group, an alkenyl group, a silyl group, an alkynyl group and a monovalent hydrocarbon cyclic or heterocyclic aromatic organic group and a part of hydrogen atoms on a ring may be substituted by a group which has no participation in a reaction. SELECTED DRAWING: None COPYRIGHT: (C)2016,JPOandINPIT