ChemicalBook > CAS DataBase List > Sodium benzenolate
Sodium benzenolate
Sodium benzenolate
- CAS No.139-02-6
- Chemical Name:Sodium benzenolate
- CBNumber:CB7306886
- Molecular Formula:C6H5NaO
- Formula Weight:116.09
- MOL File:139-02-6.mol
Sodium benzenolate Property
- Melting point >300℃
- Density 0,898 g/cm3
- RTECS SM8780000
- Flash point 28°C
- storage temp. below 5° C
- solubility DMSO (Slightly, Sonicated), Methanol (Slightly)
- form Solid
- color Pale Yellow to Pale Brown
- Specific Gravity 0.898
- Water Solubility Very soluble in water, soluble in alcoholSoluble in water, acetone and alcohol.
- Sensitive Hygroscopic
- Stability Hygroscopic
- CAS DataBase Reference 139-02-6(CAS DataBase Reference)
- FDA 21 CFR 310.545
- EWG's Food Scores 1
- FDA UNII 4NC0T56V35
- EPA Substance Registry System Sodium phenate (139-02-6)
- UNSPSC Code 12352303
Safety
- 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 Data :139-02-6(Hazardous Substances Data)
-
NFPA 704:
0 3 0
-
Symbol(GHS)
- Signal wordDanger
- Hazard statements H314
- Precautionary statements P260-P280-P301+P330+P331
Sodium benzenolate Price
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- Product name : Sodium phenoxide, 98%
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- Product number: S 3209
- Product name : Sodium phenoxide
- Purity: 98%
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- Product number: S 3209
- Product name : Sodium phenoxide
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Sodium benzenolate Chemical Properties,Usage,Production
- Chemical Properties Sodium phenate, or sodium phenoxide, NaOC6H5, is a white crystalline substance that easily dissolves in water and alcohol. It decomposes when exposed to carbon dioxide in the air. It is produced by reacting sodium hydroxide solution (not carbonate) with phenol and subsequently evaporating the mixture. Sodium phenate is commonly used in the production of sodium salicylate.
- Uses Sodium 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.
- Uses As 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).
- Definition ChEBI: Sodium phenolate is a phenolate. It has a role as a disinfectant.
- Preparation Sodium 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.
- General Description A white to reddish colored solid in the form of crystalline rods. Used as an antiseptic and in organic synthesis.
- Air & Water Reactions Decomposes in air. Soluble in water. In both cases, a corrosive alkaline solution forms that is a strong irritant to skin and eyes.
- Reactivity Profile Salts, 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.
- Hazard Strong irritant to skin and tissue.
- Safety Profile Poison 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 Methods The 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.]
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139-02-6, Sodium benzenolateRelated Search:
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- 金属有机物
- C6H5ONa3H2O
- C6H5NaO
- C6H6ONa
- NaC6H5
- C6H5ONa
- 苯酚钠溶液
- 吡非尼酮杂质3钠盐 (吡非尼酮 EP 杂质 C钠盐)
- 苯酚钠,98%
- 63苯酚钠 苯氧基钠571188-82-4
- 石炭酸鈉
- 酚鈉
- 苯鈉
- 苯氧鈉
- 苯氧基钠
- 苯氧化钠
- 苯酚钠盐
- 苯酚钠(苯酚钠盐、苯氧化钠、石炭酸鈉)
- 苯酚钠
- 139-02-6
- Amlexanox Impurity 9
- SODIUM PHENOXIDE
- SODIUM PHENOLATE
- SODIUM PHENATE
- Kjeldahl Phenol Reagent, Pure, for Determination Of Nitrogen, Fisher Chemical
- Sodium benzenolate ISO 9001:2015 REACH
- Sodium benzeneolate
- Phenoxysodium
- Sodium benzenolate
- sodium phenylate
- Natriumphenolat
- Sodium phenoxide, 20% in methanol
- Sodium phenoxide, 95%, anhydrous
- SodiuM ophenlate
- Sodiumphenoxideanhydrous
- PHENYL SODIUM
- SODIUM PHENYL
- sodiumphenolate,solid
- sodiumcarbolate
- phenolsodiumsalt
- Phenolsodium
- phenolatesodium
- phenol,sodiumsalt(solid)
- Phenol,sodiumsalt