Cas no 32266-60-7 (Azomethine-H (>90%))
Azomethine-H (>90%) Chemical and Physical Properties
Names and Identifiers
-
- 4-Hydroxy-5-((2-hydroxybenzylidene)amino)naphthalene-2,7-disulfonic acid
- Azomethine-H hydrate
- 2-HEXADECANONE
- 4-Hydroxy-5-((2-hydroxybenzylidene)amino)-naphthalene-2,7-disulfonic acid
- AZOMETHINE H
- Azomethine-H
- AZOMETHINE-H,REAGENT
- Einecs 250-975-3
- 1-(salicylideneamino)-8-hydroxynaphthalene-3,6-disulfonic acid
- 4-Hydroxy-5-(((2-hydroxyphenyl)methylene)amino)naphthalene-2,7-disulphonic acid
- 5941-07-1
- AKOS030242286
- 4-hydroxy-5-((2-hydroxybenzylidene)amino)-2,7-naphthalenedisulfonic acid
- 4-Hydroxy-5-((2-hydroxybenzylidene)amino)naphthalene-2,7-disulfonicacid
- DTXSID00954074
- AKOS016004513
- C17H13NO8S2
- NCI60_041974
- NCGC00097041-01
- NSC88947
- CHEMBL1315316
- CCG-37199
- Azomethine-H (>90%)
- (E)-4-hydroxy-5-(2-hydroxybenzylideneamino)naphthalene-2,7-disulfonic acid
- NCIStruc1_001287
- NCGC00013932-02
- ?AZOMETHINE H
- H11889
- 2,7-Naphthalenedisulfonic acid, 4-hydroxy-5-(((2-hydroxyphenyl)methylene)amino)-
- NS00089488
- 32266-60-7
- SCHEMBL3424506
- Q-200667
- NSC-88947
- NCI88947
- FT-0622531
- NCIStruc2_001778
- 4-Hydroxy-5-{[(6-oxocyclohexa-2,4-dien-1-ylidene)methyl]amino}naphthalene-2,7-disulfonic acid
- azomethine-h monosodium
- 4-hydroxy-5-[(2-hydroxyphenyl)methylideneamino]naphthalene-2,7-disulfonic acid
- NCGC00013932
- 4-Hydroxy-5-(salicylidene-amino)-2,7-naphthalenedisulfonic acid
- DB-048190
- 4-hydroxy-5-{[(E)-(2-hydroxyphenyl)methylidene]amino}naphthalene-2,7-disulfonic acid
- 4-hydroxy-5-{[(2-hydroxyphenyl)methylidene]amino}naphthalene-2,7-disulfonic acid
- DUCCKQSNXPFEGT-UHFFFAOYSA-N
- STL453813
- YWRFBXPQBUKIHP-UHFFFAOYSA-N
- 2,7Naphthalenedisulfonic acid, 4hydroxy5(((2hydroxyphenyl)methylene)amino)
- 4-hydroxy-5-[[(2-hydroxyphenyl)methylene]amino]naphthalene-2,7-disulphonic acid
- 4Hydroxy5(((2hydroxyphenyl)methylene)amino)naphthalene2,7disulphonic acid
- Azomethine H Boron Reagent
- 250-975-3
-
- MDL: MFCD00066536
- Inchi: 1S/C17H13NO8S2/c19-15-4-2-1-3-10(15)9-18-14-7-12(27(21,22)23)5-11-6-13(28(24,25)26)8-16(20)17(11)14/h1-9,19-20H,(H,21,22,23)(H,24,25,26)/b18-9+
- InChI Key: DUCCKQSNXPFEGT-GIJQJNRQSA-N
- SMILES: S(C1C=C(C2C(=CC(=CC=2C=1)S(=O)(=O)O)O)/N=C/C1C=CC=CC=1O)(=O)(=O)O
Computed Properties
- Exact Mass: 423.00800
- Monoisotopic Mass: 423.008
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 4
- Hydrogen Bond Acceptor Count: 9
- Heavy Atom Count: 28
- Rotatable Bond Count: 4
- Complexity: 930
- Covalently-Bonded Unit Count: 3
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 1
- Undefined Bond Stereocenter Count: 0
- XLogP3: 1.3
- Surface Charge: 0
- Tautomer Count: 23
- Topological Polar Surface Area: 162
Experimental Properties
- Color/Form: Odorless orange crystals
- Density: 1.823
- Melting Point: >300°C
- Boiling Point: No data available
- Flash Point: No data available
- Solubility: Soluble in Acetone, Ammonium Hydroxide, n-Butanol and Water
- Water Partition Coefficient: Soluble in acetone, ammonium hydroxide, n-butanol and water.
- PSA: 178.32000
- LogP: 4.65660
- Solubility: Not determined
- Sensitiveness: Light Sensitive
Azomethine-H (>90%) Security Information
- Signal Word:warning
- Hazard Statement: H303May be harmful if swallowed+H313Skin contact may be harmful+H333Inhalation may be harmful to the body
-
Warning Statement:
P264Thoroughly clean after treatment
P280Wear protective gloves/Wear protective clothing/Wear protective goggles/Wear a protective mask
P305If it enters the eyes
P351Rinse carefully with water for a few minutes
P338Remove the contact lens(If any)And easy to operate,Continue flushing
P337If eye irritation persists
P313Obtain medical advice/care - Safety Instruction: S24/25; S23
- RTECS:GV0220000
- Storage Condition:Sealed in dry,2-8°C
Azomethine-H (>90%) Customs Data
- HS CODE:2925290090
- Customs Data:
China Customs Code:
2925290090Overview:
2925290090 Other imines and their derivatives,And their salt.Regulatory conditions:nothing.VAT:17.0%.Tax refund rate:9.0%.MFN tariff:6.5%.general tariff:30.0%
Declaration elements:
Product Name, component content, use to
Summary:
2925290090 other imines and their derivatives; salts thereof.Supervision conditions:None.VAT:17.0%.Tax rebate rate:9.0%.MFN tariff:6.5%.General tariff:30.0%
Azomethine-H (>90%) Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | A133643-10g |
Azomethine-H hydrate |
32266-60-7 | 10g |
¥999.00 | 2021-05-25 | ||
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | A133643-1g |
Azomethine-H hydrate |
32266-60-7 | 1g |
¥199.00 | 2021-05-25 | ||
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | A133643-5g |
Azomethine-H hydrate |
32266-60-7 | 5g |
¥569.00 | 2021-05-25 | ||
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | A133643-100g |
Azomethine-H hydrate |
32266-60-7 | 100g |
¥5,599.00 | 2021-05-25 | ||
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | A133643-25g |
Azomethine-H hydrate |
32266-60-7 | 25g |
¥1,999.00 | 2021-05-25 | ||
| A FA AI SHA , SAI MO FEI SHI ER KE JI QI XIA GONG SI | 16810-2g |
Azomethine-H hydrate |
32266-60-7 | 2g |
¥808.00 | 2023-05-23 | ||
| A FA AI SHA , SAI MO FEI SHI ER KE JI QI XIA GONG SI | 16810-10g |
Azomethine-H hydrate |
32266-60-7 | 10g |
¥3121.00 | 2023-05-23 | ||
| A FA AI SHA , SAI MO FEI SHI ER KE JI QI XIA GONG SI | 16810-25g |
Azomethine-H hydrate |
32266-60-7 | 25g |
¥7436.00 | 2023-05-23 | ||
| Chemenu | CM141282-100g |
4-Hydroxy-5-((2-hydroxybenzylidene)amino)-naphthalene-2,7-disulfonic acid |
32266-60-7 | 95% | 100g |
$592 | 2021-08-05 | |
| SHANG HAI YI EN HUA XUE JI SHU Co., Ltd. | R017185-1g |
Azomethine-H (>90%) |
32266-60-7 | -H | 1g |
¥197 | 2024-05-24 |
Azomethine-H (>90%) Suppliers
Azomethine-H (>90%) Related Literature
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Olga Guselnikova,Gérard Audran,Jean-Patrick Joly,Andrii Trelin,Evgeny V. Tretyakov,Vaclav Svorcik,Oleksiy Lyutakov,Sylvain R. A. Marque Chem. Sci., 2021,12, 4154-4161
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Matthew J. Gaunt,Jinquan Yu,Jonathan B. Spencer Chem. Commun., 2001, 1844-1845
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Hanie Hashtroudi,Ian D. R. Mackinnon J. Mater. Chem. C, 2020,8, 13108-13126
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Long Deng,Qian Zou,Biao Liu,Wenhui Ye,Chengfei Zhuo,Li Chen,Ze-Yuan Deng,Ya-Wei Fan,Jing Li Food Funct., 2018,9, 4234-4245
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5. Fatty acid eutectic mixtures and derivatives from non-edible animal fat as phase change materials?Pau Gallart-Sirvent,Marc Martín,Gemma Villorbina,Mercè Balcells,Aran Solé,Luisa F. Cabeza,Ramon Canela-Garayoa RSC Adv., 2017,7, 24133-24139
Additional information on Azomethine-H (>90%)
Introduction to Azomethine-H (CAS No. 32266-60-7)
Azomethine-H, also known as CAS No. 32266-60-7, is a highly specialized chemical compound that has garnered significant attention in the scientific and industrial communities. This compound is renowned for its unique properties, which make it invaluable in various applications across multiple disciplines. The term Azomethine-H refers to a specific isomer of the azomethine class, characterized by its high purity (>90%), ensuring consistent performance in research and industrial settings.
The synthesis of Azomethine-H involves a meticulous process that ensures the compound's stability and functionality. Recent advancements in synthetic methodologies have enabled the production of Azomethine-H with unprecedented precision, minimizing impurities and enhancing its utility in demanding environments. Researchers have explored novel catalysts and reaction conditions to optimize the synthesis process, making it more efficient and scalable for large-scale production.
Azomethine-H exhibits remarkable thermal stability and excellent solubility in polar solvents, making it a preferred choice in materials science applications. Its ability to form stable complexes with metal ions has been extensively studied, particularly in the context of coordination chemistry. Recent studies have demonstrated its potential as a ligand in catalytic systems, where it enhances the selectivity and efficiency of reactions involving transition metals.
In the field of biochemistry, Azomethine-H has shown promise as a versatile reagent for protein modification and enzyme stabilization. Its ability to interact with biomolecules without compromising their functionality has opened new avenues for drug delivery systems and biotechnological applications. Scientists have leveraged its unique properties to develop innovative strategies for targeted drug delivery, where Azomethine-H serves as a stabilizing agent, ensuring the integrity of therapeutic molecules during transit.
The application of Azomethine-H extends into the realm of nanotechnology, where it plays a pivotal role in the synthesis of nanoparticles. Recent research has highlighted its ability to act as a reducing agent in green chemistry processes, facilitating the production of metal nanoparticles with controlled sizes and shapes. This capability has significant implications for catalysis, sensing technologies, and electronic devices.
Furthermore, Azomethine-H has been investigated for its potential in environmental remediation. Its capacity to bind heavy metal ions makes it an attractive candidate for water treatment applications. Studies have shown that Azomethine-H-based materials can efficiently remove pollutants such as lead and mercury from aqueous solutions, offering a sustainable solution to environmental contamination.
The demand for high-purity Azomethine-H (>90%) has driven advancements in analytical techniques for quality control. State-of-the-art methods such as high-performance liquid chromatography (HPLC) and nuclear magnetic resonance (NMR) spectroscopy are employed to ensure the compound meets stringent purity standards. These techniques provide detailed insights into the molecular structure and impurity profile of Azomethine-H, ensuring its reliability in critical applications.
In conclusion, Azomethine-H (CAS No. 32266-60-7) stands out as a versatile compound with a wide range of applications across diverse fields. Its unique properties, coupled with recent advancements in synthesis and application techniques, position it as a key player in modern scientific research and industrial innovation.
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