Identification |
Name: | Acetamide,2,2'-[(2-hydroxyethyl)imino]bis[N-(1,1-dimethyl-2-phenylethyl)-N-methyl- |
Synonyms: | Acetamide,2,2'-[(2-hydroxyethyl)imino]bis[N-(a,a-dimethylphenethyl)-N-methyl-(6CI,7CI,8CI);2,2'-[(2-Hydroxyethyl)imino]bis[N-(a,a-dimethylphenethyl)-N-methylacetamide];2-Di(N-methyl-N-phenyl-tert-butyl-carbamoylmethyl)aminoethanol;Betalgil;FH099;Mucoxin;Oxaine;Oxetacaine;Storocain;Storocaine;Topicain; |
CAS: | 126-27-2 |
EINECS: | 204-780-5 |
Molecular Formula: | C28H41N3O3 |
Molecular Weight: | 467.72 |
InChI: | InChI=1/C28H41N3O3/c1-27(2,19-23-13-9-7-10-14-23)29(5)25(33)21-31(17-18-32)22-26(34)30(6)28(3,4)20-24-15-11-8-12-16-24/h7-16,32H,17-22H2,1-6H3 |
Molecular Structure: |
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Properties |
Melting Point: | 104-105 oC |
Density: | 1.093 g/cm3 |
Stability: | No data. |
Refractive index: | 1.557 |
Water Solubility: | | |
Solubility: | <0.1 g/100 mL at 23 oC in water |
Appearance: | White powder. |
Specification: |
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).
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Storage Temperature: | Keep in a cool, dry, dark location in a tightly sealed container or cylinder. Keep away from incompatible materials, ignition sources and untrained individuals. Secure and label area. Protect containers/cylinders from physical damage. |
Usage: | Surface anesthetic used mainly orally in chronic gastritis and heartburn to analgize the gastric mucosa. |
Safety Data |
Hazard Symbols |
Xn: Harmful
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