Hydroxytetracaine
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Basic information
- CAS
490-98-2- Standard SMILES
CCCCNc1ccc(C(=O)OCCN(C)C)c(O)c1- InChIKey
DHCUQNSUUYMFGX-UHFFFAOYSA-N- Molecular formula
- C15H24N2O3
- Average molar mass
- 280.36 g/mol
- Monoisotopic mass
- 280.17869263
Overview
Hydroxytetracaine is a member of phenols and a benzoate ester. It is functionally related to a salicylic acid.
Names & identifiers
- Preferred name
- Hydroxytetracaine
- IUPAC
- 2-(dimethylamino)ethyl 4-(butylamino)-2-hydroxybenzoate
- English name
- Hydroxytetracaine
- Molecular formula
- C15H24N2O3
- Molecular weight
- 280.36
Names & synonyms
HydroxytetracaineHydroxamethocaine490-98-2RhenocainOxitetracainumOxypentocainSalicacaineHidroxitetracainaIdrossitetracainaSalicaine (anesthetic)HydroxytetracainumIdrossitetracaina [DCIT]
Show more names
Cynodal2-dimethylaminoethyl 4-(butylamino)-2-hydroxybenzoate2-dimethylaminoethyl 4-(butylamino)-2-hydroxy-benzoate4-Butylaminosalicylic acid 2-(dimethylamino)ethyl ester4-Butylamino-2-hydroxybenzoic acid 2-dimethylaminoethyl esterBenzoic acid, 4-(butylamino)-2-hydroxy-, 2-(dimethylamino)ethyl ester
Hydroxytetracainum [INN-Latin]Hidroxitetracaina [INN-Spanish]Hydroxytetracaine [INN:BAN:DCF]WIN 3546BRN 2125583UNII-8A96H4311N2-Dimethylaminoethyl 4-butylaminosalicylate2-(Dimethylamino)ethyl-4-(butylamino)salicylate
Database identifiers
- CAS
490-98-2- PubChem CID
- 71630
- DTXSID
DTXSID60197662- ChEMBL
CHEMBL2106365- ChEBI
CHEBI:135162- UNII
- 8A96H4311N
- Nikkaji
- J6.048H
Properties
Computed structural propertiesFilling in
- XLogP
- 3.9
- Topological polar surface area
- 61.8 Ų
- Hydrogen bond donors
- 2
- Hydrogen bond acceptors
- 5
- Rotatable bonds
- 9
- Heavy atoms
- 20
- Formal charge
- 0
- Complexity
- 284
Physicochemical properties
- FDA UNII
- 8 A96H4311N · 8A96H4311N
Chemistry & industry
Applications
UsesHydroxytetracaine is a local agent that can suppress or relieve pain[1].
Upstream & downstream products
Upstream raw materials
Additional notes
DefinitionChEBI: Hydroxytetracaine is a member of phenols and a benzoate ester. It is functionally related to a salicylic acid.
Related reactions
0 records
No reaction records under the current filter.
Compound notes
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