| Dimethocaine | |
|---|---|
| Salts [] | |
|---|---|
| Dimethocaine salicylate | |
| Molecular structure via molpic based on CDK |
| Physical properties [] | |
|---|---|
| Molecular mass | 278.39 g/mol [1] |
| Predicted LogP | 3.1 [1] |
| Structural Identifiers [] | |
|---|---|
| Molecular formula | C16H26N2O2 [1] |
| IUPAC name | [3-(diethylamino)-2,2-dimethylpropyl] 4-aminobenzoate [1] |
| SMILES | CCN(CC)CC(C)(C)COC(=O)C1=CC=C(C=C1)N [1] |
| InChI | InChI=1S/C16H26N2O2/c1-5-18(6-2)11-16(3,4)12-20-15(19)13-7-9-14(17)10-8-13/h7-10H,5-6,11-12,17H2,1-4H3 [1] |
| InChIKey | OWQIUQKMMPDHQQ-UHFFFAOYSA-N [1] |
| Toxicity [] | |
|---|---|
| LDLo | Mouse: - subcutaneous: 380 mg/kg - intravenous: 40 mg/kg Rabbit: - subcutaneous: 150 mg/kg - intravenous: 150 mg/kg Guinea pig: - subcutaneous: 200 mg/kg Frog: - parenteral: 860 mg/kg |
Dimethocaine
Dimethocaine (also known as 3-(Diethylamino)-2,2-dimethylpropyl 4-aminobenzoate, (3-Diethylamino-2,2-dimethyl)propyl 4-aminobenzoat, 1-Propanol, 3-(diethylamino)-2,2-dimethyl-, 4-aminobenzoate, RefChem:134182, Larocaine, 1-Propanol, 3-(diethylamino)-2,2-dimethyl-, p-aminobenzoate, 3-Diethylamino-2,2-dimethylpropyl 4-Aminobenzoate, 2-Dicyclohexylphosphino-2',6'-bis(N,N-dimethylamino)biphenyl; 2'-(Dicyclohexylphosphino)-N2,N2,N6,N6-tetramethylbiphenyl-2,6-diamine, 4-Aminobenzoesaeure-3-diethylamino-2,2-dimethylproplylester or 1-Propanol, 2-[(diethylamino)methyl]-2-methyl-, 1-(4-aminobenzoate)) is a sodium channel blocker and stimulant substance of the carboxylic acid class.
Chemistry
Salts []
Dimethocaine is typically found in the form of its salicylate salt.
Stereochemistry []
Dimethocaine is a achiral mixture
Subjective effects
| Anodyne Usernotes [] | |
|---|---|
| 0xea / Dimethocaine[freebase][citrate] via Intravenous and Vaporized |
|
Legal status
- Germany: Dimethocaine is a Anlage II substance.
- United Kingdom: Dimethocaine is a PSA substance.
See also []
External links []
References []
National Center for Biotechnology Information. PubChem Compound Summary for CID 7177, Dimethocaine. Accessed October 7, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/7177
U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Dimethocaine. UNII: R3L4A6GOWZ. Global Substance Registration System. Accessed October 7, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/R3L4A6GOWZ
Anodyne