Sodium benzenolate

Sodium benzenolate Basic information
Preparation
Product Name:Sodium benzenolate
Synonyms:Phenol,sodiumsalt;phenol,sodiumsalt(solid);phenolatesodium;Phenolsodium;phenolsodiumsalt;sodiumcarbolate;sodiumphenolate,solid;SODIUM PHENATE
CAS:139-02-6
MF:C6H5NaO
MW:116.09
EINECS:205-347-3
Product Categories:
Mol File:139-02-6.mol
Sodium benzenolate Structure
Sodium benzenolate Chemical Properties
Melting point >300℃
density 0,898 g/cm3
RTECS SM8780000
Fp 28°C
storage temp. below 5° C
solubility DMSO (Slightly, Sonicated), Methanol (Slightly)
form Solid
color Pale Yellow to Pale Brown
Specific Gravity0.898
Water Solubility Very soluble in water, soluble in alcoholSoluble in water, acetone and alcohol.
Sensitive Hygroscopic
Stability:Hygroscopic
CAS DataBase Reference139-02-6(CAS DataBase Reference)
EPA Substance Registry SystemSodium phenate (139-02-6)
Safety Information
Hazard Codes C
Risk Statements 34
Safety Statements 26-36/37/39-45
RIDADR 3286
TSCA No
HazardClass 8
PackingGroup III
HS Code 2907110000
Hazardous Substances Data139-02-6(Hazardous Substances Data)
MSDS Information
ProviderLanguage
ALFA English
Sodium benzenolate Usage And Synthesis
PreparationSodium phenoxide was freshly prepared by adding sodium metal to phenol (0.45  g, 4.8 mmol) dissolved in diethyl ether (15 cm3), under an atmosphere of dry nitrogen.  This was refluxed with (11) (1.0 g, 2.8 mmol) for 23 h. Following evaporation of the  ether, water (20 cm3) was added and the mixture extracted into DCM. The DCM solution  was dried (MgS04) and evaporated to give a solid (1.2 g). Fractional sublimation and  recrystallisation from acetonitrile gave recovery of 2,4,6-tribromo-3,5-difluoropyridine  (0.8 g, 80%) and 3-phenoxy-5-fluoro-2,4,6-tribromopyridine (0.2 g, 20%), m.p. 100±1  OC (Found: C, 31.3; H, 1.1; N, 2.9. C11H5Br3FNO requires C, 31.0; H, 1.2; N,  3.3%); IR spectrum no. 15; mass spectrum no. 15; nmr spectrum no. 19.
Chemical PropertiesWhite, deliquescent crystals. Soluble in water and alcohol; decomposed by carbon dioxide in the air.
Chemical PropertiesSodium phenate, sodium phenoxide, sodium phenolate, NaOC6H5, white solid, soluble, formed by reaction of sodium hydroxide (not carbonate) solution and phenol, and then evaporating. Used in the preparation of sodium salicylate.
UsesSodium phenoxide is used as a precursor to aryl ethers and involved in the preparation of phenyl ethers and metal phenolates. It serves as an antiseptic and used in organic synthesis.
UsesAs a general disinfectant, either in solution or mixed with slaked lime, etc., for toilets, stables, cesspools, floors, drains, etc.; for the manufacture of colorless or light-colored artificial resins, many medical and industrial organic Compounds and dyes; as a reagent in chemical analysis. Pharmaceutic aid (preservative).
DefinitionChEBI: Sodium phenolate is a phenolate. It has a role as a disinfectant.
General DescriptionA white to reddish colored solid in the form of crystalline rods. Used as an antiseptic and in organic synthesis.
Air & Water ReactionsDecomposes in air. Soluble in water. In both cases, a corrosive alkaline solution forms that is a strong irritant to skin and eyes.
Reactivity ProfileSalts, basic, such as SODIUM PHENOLATE, are generally soluble in water. The resulting solutions contain moderate concentrations of hydroxide ions and have pH's greater than 7.0. They react as bases to neutralize acids. These neutralizations generate heat, but less or far less than is generated by neutralization of the bases in reactivity group 10 (Bases) and the neutralization of amines. They usually do not react as either oxidizing agents or reducing agents but such behavior is not impossible.
HazardStrong irritant to skin and tissue.
Safety ProfilePoison by subcutaneous route. A corrosive irritant to skin, eyes, and mucous membranes. When heated to decomposition it emits toxic fumes of Na2O. See also PHENOL and SODIUM HYDROXIDE.
Purification MethodsThe ground powder is washed with Et2O, then heated at 60o/1mm for 12 to 24hours to remove any free phenol and solvent. [Kornblum & Lurie J Am Chem Soc 81 2710 1959, Beilstein 6 I 718.]
Sodium benzenolate Preparation Products And Raw materials
Preparation Products2-BROMOETHYL PHENYL SULFIDE-->(4-BROMOPHENOXY)ACETIC ACID ETHYL ESTER-->2-PHENOXYPROPIONYL CHLORIDE-->Bromobenzene-->2,6-Diiodo-4-nitrophenol-->4-PHENOXYPHTHALONITRILE-->1,1,2,2-Tetrakis(4-hydroxyphenyl)ethane-->Propoxybenzene-->3-PHENOXYBROMOBENZENE-->PHENYL PROPARGYL ETHER-->2-BROMO-2-BUTENE-->4-Phenoxybutyl bromide-->Ethylene glycol diphenyl ether-->ROSOLIC ACID-->Dibenz[b,e]oxepin-11(6H)-one-->4-Phenoxypyridine
Sodium bicarbonate sodium Sodium 2-hydroxybenzenesulfonate Sodium triacetoxyborohydride Sodium 2-nitrophenoxide Sodium sulfate Anisole (Trifluoromethoxy)benzene Sodium pentachlorophenolate Sodium 4-nitrophenoxide Benzoylacetonitrile p-Anisic acid Sodium benzenolate Sodium citrate p-Anisaldehyde Sodium hydroxide Sodium chlorite Sodium 2-biphenylate

Email:[email protected] [email protected]
Copyright © 2024 Mywellwork.com All rights reserved.