3,4,5,6-四溴酚磺酞 - Names and Identifiers
Name | 3,4,5,6-Tetrabromophenolsulfonephthalein
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Synonyms | Nsc624919 Aids044105 Aids-044105 Tetrabromosulfonephthalein 4,5,6,7-Tetrabromophenolsulfophthalein 4,5,6,7-Tetrabromophenolsulfonephthalein 3,4,5,6-Tetrabromophenolsulfonephthalein 4,5,6,7-Tetrabromo-3,3-bis(p-hydroxyphenyl)-3H-2,1-benzoxathiole 1,1-dioxide
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CAS | 77172-72-6 123333-63-1 128915-86-6
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InChI | InChI=1/C19H10Br4O5S/c20-14-13-18(17(23)16(22)15(14)21)29(26,27)28-19(13,9-1-5-11(24)6-2-9)10-3-7-12(25)8-4-10/h1-8,24-25H |
3,4,5,6-四溴酚磺酞 - Physico-chemical Properties
Molecular Formula | C19H10Br4O5S
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Molar Mass | 669.96 |
Density | 2.199±0.06 g/cm3(Predicted) |
Melting Point | 270-271 °C |
Boling Point | 696.1±55.0 °C(Predicted) |
Flash Point | 374.8°C |
Vapor Presure | 5.03E-20mmHg at 25°C |
pKa | 7.88±0.50(Predicted) |
Storage Condition | Sealed in dry,Room Temperature |
Refractive Index | 1.743 |
3,4,5,6-四溴酚磺酞 - Risk and Safety
Hazard Symbols | Xi - Irritant
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Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin.
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Safety Description | 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
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WGK Germany | 3 |
HS Code | 38220090 |
3,4,5,6-四溴酚磺酞 - Introduction
3,4,5, is an organic compound. The following is a description of the nature, use, method and safety information:
Nature:
-Appearance: 3,4,5, red crystals or powder.
-Solubility: It has better solubility in organic solvents, but lower solubility in water.
- pH indicator: It is an acid-base indicator with a color range of red to yellow.
-Thermal stability: It has a certain thermal stability at high temperatures.
Use:
-Acid-base indicator: 3,4,5, widely used as acid-base indicator, can be used to determine the acid-base properties and pH value of the solution.
-Laboratory applications: It can also be used for color indicators, catalysts and spectral analysis in chemical laboratories.
Preparation Method:
- 3,4,5, benzenesulfonyl chloride is usually synthesized by reacting 3,4,5,6-tetrabromophenol with benzenesulfonyl chloride. This reaction produces a phthalein ring and a bromine atom replaces the hydrogen atom on the benzene ring.
-The synthesis method can be improved and optimized according to specific experimental conditions and uses.
Safety Information:
- 3,4,5, in general, non-toxic to the human body.
-However, it may cause irritation to the eyes and skin. Therefore, when handling, wear appropriate personal protective equipment to avoid direct contact.
-During storage and use, avoid contact with oxidants and strong acids to avoid dangerous chemical reactions.
Last Update:2024-04-09 20:48:19