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Sodium benzenolate

Sodium benzenolate Structure
CAS No.
139-02-6
Chemical Name:
Sodium benzenolate
Synonyms
SODIUM PHENOXIDE;SODIUM PHENATE;SODIUM PHENOLATE;Phenolsodium;PHENYL SODIUM;SODIUM PHENYL;Phenoxysodium;phenolatesodium;sodiumcarbolate;Natriumphenolat
CBNumber:
CB7306886
Molecular Formula:
C6H5NaO
Molecular Weight:
116.09
MOL File:
139-02-6.mol
Modify Date:
2023/11/10 11:05:08

Sodium benzenolate Properties

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)
EPA Substance Registry System Sodium phenate (139-02-6)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS05
Signal word  Danger
Hazard statements  H314
Precautionary statements  P260-P280-P301+P330+P331
Hazard Codes  C
Risk Statements  34
Safety Statements  26-36/37/39-45
RIDADR  3286
TSCA  No
HazardClass  8
PackingGroup  III
HS Code  2907110000
NFPA 704
0
3 0

Sodium benzenolate price More Price(4)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
ALFA India ALF-B25002-30 Sodium phenoxide, 98% 139-02-6 250g ₹44069 2022-05-26 Buy
ALFA India ALF-B25002-18 Sodium phenoxide, 98% 139-02-6 50g ₹8046 2022-05-26 Buy
ottokemi S 3209 Sodium phenoxide 98% 139-02-6 50gm ₹8604 2022-05-26 Buy
ottokemi S 3209 Sodium phenoxide 98% 139-02-6 250gm ₹43902 2022-05-26 Buy
Product number Packaging Price Buy
ALF-B25002-30 250g ₹44069 Buy
ALF-B25002-18 50g ₹8046 Buy
S 3209 50gm ₹8604 Buy
S 3209 250gm ₹43902 Buy

Sodium benzenolate Chemical Properties,Uses,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

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).

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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Phenol,sodiumsalt phenol,sodiumsalt(solid) phenolatesodium Phenolsodium phenolsodiumsalt sodiumcarbolate sodiumphenolate,solid SODIUM PHENYL PHENYL SODIUM Sodiumphenoxideanhydrous SodiuM ophenlate Sodium phenoxide, 95%, anhydrous Sodium phenoxide, 20% in methanol Natriumphenolat sodium phenylate Sodium benzenolate Phenoxysodium Sodium benzeneolate Sodium benzenolate ISO 9001:2015 REACH Kjeldahl Phenol Reagent, Pure, for Determination Of Nitrogen, Fisher Chemical SODIUM PHENATE SODIUM PHENOLATE SODIUM PHENOXIDE Amlexanox Impurity 9 139-02-6 C6H5ONa NaC6H5 C6H6ONa C6H5NaO C6H5ONa3H2O