Oxethazaine Chemical Properties

Melting point:

104-105°C

Boiling point:

570.1°C (rough estimate)

Density 

1.0974 (rough estimate)

refractive index 

1.7800 (estimate)

storage temp. 

Refrigerator

solubility 

Practically insoluble in water; freely soluble in methanol; soluble in ethyl acetate.

pka

14.62±0.10(Predicted)

color 

White to Off-White

Water Solubility 

<0.1 g/100 mL at 23 ºC

CAS DataBase Reference

126-27-2(CAS DataBase Reference)

EPA Substance Registry System

Oxethazaine (126-27-2)

Safety Information

Hazard Codes 

Xn

Risk Statements 

22

Safety Statements 

36

WGK Germany 

3

RTECS 

AC3325000

Toxicity

LD50 oral in rat: 1gm/kg

MSDS

• Language:English Provider:2-Di(N-methyl-N-phenyl-tert-butyl-carbamoylmethyl)aminoethanol
• Language:English Provider:SigmaAldrich

Oxethazaine Usage And Synthesis

Chemical Properties

White Solid

Originator

Oxaine,Wyeth,US,1960

Uses

A potent local anesthetic that is active even in acidic conditions. It is used (usually in combination with an antacid) for the relief of pain associated with peptic ulcer disease or esophagitis.

Uses

antiviral, RT inhibitor

Definition

ChEBI: Oxethazaine is an amino acid amide.

Manufacturing Process

Chlor-N-methyl-N-ω-phenyl-tert-butyl acetamide (23.95 g) (0.1 mol) is added to n-butanol (150.0 cc) containing anhydrous potassium carbonate (50.0 g). To the stirred refluxing solution is added dropwise freshly distilled ethanolamine (3.1 g) (0.05 mol). Stirring and refluxing is maintained for twenty hours. Upon cooling the solution is filtered; the residue is washed with n-butanol. The combined filtrates are washed with aqueous sodium carbonate solution then water and finally dried over anhydrous magnesium sulfate. The solvent is distilled under vacuum leaving a dry solid residue. The residue is dissolved in dry benzene to which is added n-hexane to crystallize the product melting at 104°C to 104.5°C. Yield 71-73%. Analysis-Carbon: calc. 71.9%; found 71.93%; hydrogen: calc. 8.8%; found 8.9%; nitrogen: calc. 9.0%; found 9.0%.
To make the hydrochloride salt, the bisacetamide or, by another name, 1,11diphenyl-2,2,3,9,10,10-hexamethyl-4,8-diketo-6-(β-hydroxyethyl)-3,6,9triazaundecane is dissolved in n-butanol. The solution is chilled and then dry hydrogen chloride gas is passed into the solution causing an oil to separate. To the heavy oil ether is added and then stirred causing crystallization to occur. MP 146°C to 147°C. Analysis for nitrogen: calc. 83%. found 8.2%.
To make the acetate salt, the bisacetamide (4.7 g) (0.01 mol) is dissolved in ethyl acetate to which is added glacial acetic acid (0.6 g) (0.01 mol). Ether is added to precipitate the acetate as a gum which is washed with hexane, and finally added to dry ether. Allow to stand for crystallization. MP 141°C. Analysis for nitrogen: calc. 8.0%; found 8.2%.
Other salts are: sulfate, MP 56°C; acid oxalate, MP 127°C; tartrate, MP 45°C; picrate, MP 151°C to 152°C.

Therapeutic Function

Local anesthetic

General Description

White powder.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

A hydroxylated amide. Organic amides/imides react with azo and diazo compounds to generate toxic gases. Flammable gases are formed by the reaction of organic amides/imides with strong reducing agents. Amides are very weak bases (weaker than water). Imides are less basic yet and in fact react with strong bases to form salts. That is, they can react as acids. Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile. The combustion of these compounds generates mixed oxides of nitrogen (NOx).

Fire Hazard

Flash point data are not available for Oxethazaine, but Oxethazaine is probably combustible.

Oxethazaine(126-27-2)Related Product Information

• 3,4'-DIAMINODIPHENYLMETHANE
• tert-Butyl acetate
• Monoethanolamine
• 2,2-Diethoxyethylamine
• 2-(4-Aminophenyl)ethanol
• Thiophanate-methyl
• Benzocaine
• tert-Butanol
• Articaine
• PHENYL VALERATE
• 2-AMINO-1-PHENYLETHANOL
• Tribenuron methyl
• Mepivacaine
• tert-Butyl peroxyacetate
• Mepivacaine hydrochloride
• Kresoxim-methyl
• Methyl salicylate
• Methyl