sodium [3-[[2,4-dihydroxy-5-[(4-nitro-2-sulphophenyl)azo]phenyl]azo]-2-hydroxy-5-nitrobenzene-1-sulphonato(4-)]ferrate(1-)
sodium [3-[[2,4-dihydroxy-5-[(4-nitro-2-sulphophenyl)azo]phenyl]azo]-2-hydroxy-5-nitrobenzene-1-sulphonato(4-)]ferrate(1-)
CAS: 84878-22-8
Molecular Formula: C18H8FeN6NaO13S2
sodium [3-[[2,4-dihydroxy-5-[(4-nitro-2-sulphophenyl)azo]phenyl]azo]-2-hydroxy-5-nitrobenzene-1-sulphonato(4-)]ferrate(1-) - Names and Identifiers
sodium [3-[[2,4-dihydroxy-5-[(4-nitro-2-sulphophenyl)azo]phenyl]azo]-2-hydroxy-5-nitrobenzene-1-sulphonato(4-)]ferrate(1-) - Physico-chemical Properties
| Molecular Formula | C18H8FeN6NaO13S2 |
| Molar Mass | 659.25329 |
sodium [3-[[2,4-dihydroxy-5-[(4-nitro-2-sulphophenyl)azo]phenyl]azo]-2-hydroxy-5-nitrobenzene-1-sulphonato(4-)]ferrate(1-) - Introduction
sodium [3-[[2,4-dihydroxy-5-[(4-nitro-2-sulfophenyl) azo]phenyl]azo]-Na-Ferrioxalate (4-)]ferrate(1-) is an organic polymer compound, its chemical structure contains hydroxyl, Nitro and sulfonic acid groups and other functional groups.
Properties: Na-Ferrioxalate is a dark red crystalline solid, soluble in water and organic solvents. It has strong stability and is not easy to decompose at room temperature.
Uses: Na-Ferrioxalate have a variety of applications in chemical research. Because of its absorption and emission characteristics of visible light, it can be used to prepare photosensitive materials, photocatalytic materials, photoelectric conversion devices, etc. In addition, Na-Ferrioxalate can also be used as dyes, catalysts and other fields.
preparation method: the preparation of Na-Ferrioxalate usually adopts chemical reaction method, and the specific process includes the steps of synthesis of dihydroxy terephthalic acid, preparation of azo compounds, and further reaction to obtain Na-Ferrioxalate.
Safety Information: Na-Ferrioxalate are organic compounds and should be used with the same care as any other chemical. Avoid contact with other substances such as oxidants, acids, etc. to prevent unsafe reactions. During operation and storage, attention should be paid to protective measures to avoid inhalation, contact with skin or swallowing. In the event of an accident or discomfort, a doctor should be called immediately and details of the compound should be provided.
Properties: Na-Ferrioxalate is a dark red crystalline solid, soluble in water and organic solvents. It has strong stability and is not easy to decompose at room temperature.
Uses: Na-Ferrioxalate have a variety of applications in chemical research. Because of its absorption and emission characteristics of visible light, it can be used to prepare photosensitive materials, photocatalytic materials, photoelectric conversion devices, etc. In addition, Na-Ferrioxalate can also be used as dyes, catalysts and other fields.
preparation method: the preparation of Na-Ferrioxalate usually adopts chemical reaction method, and the specific process includes the steps of synthesis of dihydroxy terephthalic acid, preparation of azo compounds, and further reaction to obtain Na-Ferrioxalate.
Safety Information: Na-Ferrioxalate are organic compounds and should be used with the same care as any other chemical. Avoid contact with other substances such as oxidants, acids, etc. to prevent unsafe reactions. During operation and storage, attention should be paid to protective measures to avoid inhalation, contact with skin or swallowing. In the event of an accident or discomfort, a doctor should be called immediately and details of the compound should be provided.
Last Update：2024-04-09 21:04:16
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sodium [3-[[2,4-dihydroxy-5-[(4-nitro-2-sulphophenyl)azo]phenyl]azo]-2-hydroxy-5-nitrobenzene-1-sulphonato(4-)]ferrate(1-)
2-chloro-3-(hydroxyMethylene)cyclohex-1-enecarbaldehyde
2-氰基-N-(2,6-二乙基苯基)乙酰胺
4-(Trifluoromethyl)isoindolin-1-one
Purine riboside triphosphate
苯基甘油醇醇
3'-Azido-3'-deoxy-beta-L-uridine
Fema 2302
3-三氟甲基-5-溴吡啶-2-甲酸
Maxx 90
2-chloro-3-(hydroxyMethylene)cyclohex-1-enecarbaldehyde
2-氰基-N-(2,6-二乙基苯基)乙酰胺
4-(Trifluoromethyl)isoindolin-1-one
Purine riboside triphosphate
苯基甘油醇醇
3'-Azido-3'-deoxy-beta-L-uridine
Fema 2302
3-三氟甲基-5-溴吡啶-2-甲酸
Maxx 90