Cas no 10294-31-2 (Gold(I) iodide)
Gold(I) iodide Chemical and Physical Properties
Names and Identifiers
-
- Gold(I) iodide
- gold monoiodide
- GoldIiodideyellowgreenpowder
- gold(1+) iodide
- gold iodide
- Aurous iodide
- Gold(I) Iodid
- goldiodide(aui)
- GOLD(I) IODIDE, 99.9%
- GOLD(I) IODIDE (61%AU)
- GOLD(I) IODIDE (99.9%-AU)
- Gold(I)iodide,99%(99.9+%-Au)
- EINECS 233-656-3
- MFCD00014175
- AKOS015911151
- CS-0106011
- T1UDV7ES1A
- iodogold
- Gold iodide (AuI)
- Gold(I) iodide, 99.9% trace metals basis
- UNII-T1UDV7ES1A
- DTXSID9065027
- 10294-31-2
- Q4202650
-
- MDL: MFCD00014175
- Inchi: 1S/Au.HI/h;1H/q+1;/p-1
- InChI Key: ATGIETUGWDAYPU-UHFFFAOYSA-M
- SMILES: [Au]I
Computed Properties
- Exact Mass: 323.871
- Monoisotopic Mass: 323.871
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 0
- Heavy Atom Count: 2
- Rotatable Bond Count: 0
- Complexity: 2
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Surface Charge: 0
- Tautomer Count: nothing
- XLogP3: nothing
- Topological Polar Surface Area: 0A^2
Experimental Properties
- Color/Form: The light yellow crystal belongs to the tetragonal system
- Density: 8.25?g/mL?at 25?°C(lit.)
- Melting Point: 120?°C (dec.) (lit.)
- Boiling Point: No data available
- Flash Point: No data available
- Water Partition Coefficient: Insoluble in water. Soluble in alkali iodide, cyanide solutions. Decomposes in warm acids
- Stability/Shelf Life: store cold
- PSA: 0
- LogP: 0.88320
- Sensitiveness: Moisture Sensitive
- Solubility: Insoluble in water.
- Vapor Pressure: No data available
Gold(I) iodide Security Information
-
Symbol:
- Signal Word:Warning
- Hazard Statement: H315-H319-H335
- Warning Statement: P261-P305+P351+P338
- Hazardous Material transportation number:UN3260
- WGK Germany:3
- Hazard Category Code: 36/37/38
- Safety Instruction: 26-37/39
-
Hazardous Material Identification:
- Risk Phrases:36/37/38
- Safety Term:26-37/39
- HazardClass:8
- PackingGroup:III
- TSCA:Yes
- Storage Condition:Moisture Sensitive. Ambient temperatures.
Gold(I) iodide Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | 79-2000-1g |
Gold(I) iodide |
10294-31-2 | 99%(99.9+%-Au) | 1g |
1995.0CNY | 2021-07-08 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | 79-2000-5g |
Gold(I) iodide |
10294-31-2 | 99%(99.9+%-Au) | 5g |
7980.0CNY | 2021-07-08 | |
| SU ZHOU XIN JIA YUAN HUA XUE Technology Co., Ltd. | lj2101-100mg |
Gold(I) iodide |
10294-31-2 | 100mg |
¥0.0 | 2024-07-19 | ||
| abcr | AB120558-1 g |
Gold(I) iodide, 99% (99.9%-Au); . |
10294-31-2 | 99% | 1 g |
€215.00 | 2023-07-20 | |
| abcr | AB120558-5 g |
Gold(I) iodide, 99% (99.9%-Au); . |
10294-31-2 | 99% | 5 g |
€838.00 | 2023-07-20 | |
| BAI LING WEI Technology Co., Ltd. | 79-2000-1g |
Gold(I) iodide, 99% (99.9+%-Au) |
10294-31-2 | 99% (99.9+%-Au) | 1g |
¥ 2475 | 2022-04-25 | |
| BAI LING WEI Technology Co., Ltd. | 79-2000-5g |
Gold(I) iodide, 99% (99.9+%-Au) |
10294-31-2 | 99% (99.9+%-Au) | 5g |
¥ 9870 | 2022-04-25 | |
| XI GE MA AO DE LI QI ( SHANG HAI ) MAO YI Co., Ltd. | 398411-1G |
Gold(I) iodide |
10294-31-2 | 1g |
¥2878.86 | 2023-12-07 | ||
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | 79-2000-1g |
Gold(I) iodide |
10294-31-2 | 99%(99.9+%-Au) | 1g |
1995CNY | 2021-05-08 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | 79-2000-5g |
Gold(I) iodide |
10294-31-2 | 99%(99.9+%-Au) | 5g |
7980CNY | 2021-05-08 |
Gold(I) iodide Suppliers
Gold(I) iodide Related Literature
-
C. M. Harris,R. S. Nyholm J. Chem. Soc. 1957 63
-
2. 728. The constitution of complex metallic salts. Part XXII. The stereochemistry of four-co-ordinated gold(I) salts and some related gold(III) saltsM. Davis,Frederick G. Mann J. Chem. Soc. 1964 3791
-
Mi Jang,Tran Quang Trung,Jin-Heak Jung,Bo-Yeong Kim,Nae-Eung Lee Phys. Chem. Chem. Phys. 2014 16 4098
-
4. Structural, far-infrared and 31P nuclear magnetic resonance studies of two-co-ordinate complexes of tris(2,4,6-trimethoxyphenyl)phosphine with gold(I) halidesLisa-Jane Baker,Raymond C. Bott,Graham A. Bowmaker,Peter C. Healy,Brian W. Skelton,Peter Schwerdtfeger,Allan H. White J. Chem. Soc. Dalton Trans. 1995 1341
-
5. Halogenocarbonyl complexes of goldDaniela Belli Dell'Amico,Fausto Calderazzo,Pierluigi Robino,Annalaura Segre J. Chem. Soc. Dalton Trans. 1991 3017
Additional information on Gold(I) iodide
Gold(I) Iodide: A Comprehensive Overview
Gold(I) iodide, also known as iodoaurum, is a chemical compound with the CAS registry number CAS No. 10294-31-2. This compound has garnered significant attention in the fields of chemistry and materials science due to its unique properties and versatile applications. In this article, we will delve into the characteristics, synthesis, applications, and recent advancements related to gold(I) iodide, providing a comprehensive understanding of this intriguing compound.
The chemical formula for gold(I) iodide is AuI, and it exists in a crystalline form with a bright yellow color. It is sparingly soluble in water but exhibits higher solubility in polar solvents such as ethanol and acetone. The compound is stable under normal conditions but can decompose upon heating or exposure to light, releasing toxic fumes of hydrogen iodide (HI). These properties make it essential to handle gold(I) iodide with care in laboratory settings.
Gold(I) iodide plays a pivotal role in various chemical reactions, particularly in the synthesis of organometallic compounds and catalytic processes. One of its most notable applications is in the formation of gold nanoparticles, which have found extensive use in electronics, medicine, and environmental remediation. Recent studies have highlighted the potential of gold(I) iodide-based catalysts in promoting selective reactions, such as the oxidation of alcohols to ketones or aldehydes under mild conditions.
The synthesis of gold(I) iodide typically involves the reaction of metallic gold with elemental iodine (I?) under controlled conditions. This process can be optimized by adjusting parameters such as temperature and pressure to achieve high yields of pure product. Researchers have also explored alternative methods, including the use of ionic liquids or microwave-assisted synthesis, to enhance the efficiency and sustainability of gold(I) iodide production.
In terms of applications, gold(I) iodide has been extensively used as a precursor for gold nanoparticles due to its ability to facilitate controlled nucleation and growth processes. These nanoparticles exhibit unique optical properties, making them valuable for applications in sensing, imaging, and drug delivery systems. Additionally, gold(I) iodide-based catalysts have shown promise in promoting enantioselective reactions, which are critical for the production of chiral pharmaceuticals.
A recent breakthrough in the field involves the use of gold(I) iodide-stabilized nanoparticles for environmental cleanup applications. These nanoparticles can effectively adsorb heavy metal ions from contaminated water sources, offering a sustainable solution to water pollution challenges. Furthermore, ongoing research is exploring the potential of gold(I) iodide strong>-based materials for energy storage devices such as supercapacitors and batteries.
In conclusion, gold(I) iodide
10294-31-2 (Gold(I) iodide) Related Products
- 2098070-20-1(2-(3-(Pyridin-3-yl)-1H-pyrazol-1-yl)acetimidamide)
- 2680771-01-9(4-cyclopentyl-3-{(prop-2-en-1-yloxy)carbonylamino}butanoic acid)
- 1444113-98-7(N-(3-cyanothiolan-3-yl)-2-[(2,2,2-trifluoroethyl)sulfanyl]pyridine-4-carboxamide)
- 332062-08-5(Fmoc-S-3-amino-4,4-diphenyl-butyric acid)
- 1270529-38-8(1,2,3,4,5,6-Hexahydro-[2,3]bipyridinyl-6-ol)
- 941977-17-9(N'-(3-chloro-2-methylphenyl)-N-2-(dimethylamino)-2-(naphthalen-1-yl)ethylethanediamide)
- 2138166-62-6(2,2-Difluoro-3-[methyl(2-methylbutyl)amino]propanoic acid)
- 89640-58-4(2-Iodo-4-nitrophenylhydrazine)
- 1449132-38-0(3-Fluoro-5-(2-fluoro-5-methylbenzylcarbamoyl)benzeneboronic acid)
- 2034271-14-0(2-(1H-indol-3-yl)-N-{[6-(thiophen-2-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl]methyl}acetamide)