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4-phenoxy-pheno

4-Phenoxyphenol

CAS: 831-82-3

Molecular Formula: C12H10O2

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4-phenoxy-pheno - Names and Identifiers

Name 4-Phenoxyphenol
Synonyms POP
4-Phenoxyphenol
P-PHENOXYPHENOL
4-phenoxy-pheno
phenol, 4-phenoxy-
Phenol, p-phenoxy-
Phenol, 4-phenoxy-
o-Phenylhydroquinone
4-PHENOXYPHENOL FOR SYNTHESIS
CAS 831-82-3
EINECS 212-611-1
InChI InChI=1/C12H10O2/c13-10-6-8-12(9-7-10)14-11-4-2-1-3-5-11/h1-9,13H
InChIKey ZSBDGXGICLIJGD-UHFFFAOYSA-N

4-phenoxy-pheno - Physico-chemical Properties

Molecular FormulaC12H10O2
Molar Mass186.21
Density1.1032 (rough estimate)
Melting Point80-84 °C (lit.)
Boling Point177-180°C (11 mmHg)
Flash Point177-180°C/9mm
Water Solubilityinsoluble
Solubility toluene: 0.1g/mL, clear
Vapor Presure0.01-0.121Pa at 25℃
AppearanceSolid
Colorcolorless to light brown
BRN2047182
pKa10.07±0.13(Predicted)
Storage ConditionInert atmosphere,Room Temperature
StabilityStable. Combustible. Incompatible with strong oxidizing agents.
Refractive Index1.6010 (estimate)
MDLMFCD00002331
Physical and Chemical Properties

Melting Point: 83 - 85

Boiling Point: 177-180 at 11mm Hg

4-phenoxy-pheno - Risk and Safety

Hazard SymbolsXi - Irritant
Irritant
Risk Codes36/37/38 - Irritating to eyes, respiratory system and skin.
Safety DescriptionS26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36 - Wear suitable protective clothing.
S37/39 - Wear suitable gloves and eye/face protection
WGK Germany3
TSCAYes
HS Code29095090
Hazard NoteIrritant

4-phenoxy-pheno - Reference Information

LogP3.38-3.4 at 25℃
NIST chemical information information provided by: webbook.nist.gov (external link)
EPA chemical substance information information provided by: ofmpeb.epa.gov (external link)
Use for the use of high-efficiency, low-toxicity pesticides,
synthesis of fly ethers
4-hydroxy diphenyl ether, also known as 4-phenoxyphenol, is an intermediate of carbamate insecticides such as dioxyvere, and the sanitary insecticide pyripropyl ether.
production method There are many preparation methods of 4-hydroxy diphenyl ether, among which the two process routes have low raw material cost and simple process. Hydroquinone and bromobenzene reaction with hydroquinone as raw material, add dimethyl sulfoxide solvent and 96% potassium hydroxide solution, at the same time into the nitrogen, stirring heated to 140 ℃, slowly drop the bromobenzene solution, in (145±5) the reaction time was 8H at ℃. After completion of the reaction, the aqueous phase was acidified by hydrochloric acid to precipitate crystals, and the yield was 88%-89%. P-chlorophenol method to a 2.50 ml three-head bottle equipped with a thermometer, a water separator and a magnetic stirrer were added 235g (42.1 mol) of phenol, 0.75g (mol) of sodium hydroxide and ML of toluene, and the separated water was heated. After desolvation, 64.3g(0.50 mol) of p-chlorophenol was added dropwise and 175g of copper salt was added as a catalyst, followed by reaction at ° C. For 8 hours. After recovery of phenol, acidification was performed with dilute hydrochloric acid. It was extracted with ether and washed with water. After drying and distillation, the 145~152 ℃(800Pa) fraction was collected to obtain 60g of product, yield 64%,m. p. 83~84 degrees C (literature value m. p. 85~86 degrees C).
Last Update:2024-04-10 22:29:15
4-phenoxy-pheno
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Mobile: +86-17551318830
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SHANGHAI ACMEC BIOCHEMICAL TECHNOLOGY CO., LTD.
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Email: sales@chinaskyrun.com
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Wechat: chinaskyrun
Shanghai Yuanye Bio-Technology Co., Ltd.
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Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
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View History
4-phenoxy-pheno
氢化三丁锡
35189-28-7
1123-19-9
18800-74-3
130433-68-0
914952-37-7
927822-18-2
分散土耳其玉GL
330786-25-9
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