<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <version>1.0</version>
  <creation_date>2026-04-03 05:18:53 UTC</creation_date>
  <update_date>2026-08-19 07:12:54 UTC</update_date>
  <accession/>
  <common_name>3,5-Pyridinedicarboxylic acid, 1,4-dihydro-2,4,6-trimethyl-, diethyl ester</common_name>
  <class>SmallMolecule</class>
  <description>3,5-Pyridinedicarboxylic acid, 1,4-dihydro-2,4,6-trimethyl-, diethyl ester is an organic compound with the chemical formula C14H21N1O4 and an average molecular weight of 267.32 g/mol. 3,5-Pyridinedicarboxylic acid, 1,4-dihydro-2,4,6-trimethyl-, diethyl ester belongs to the hydropyridines, a subclass of pyridines and derivatives within the organic compounds.

This substance is categorized within the superclass of organoheterocyclic compounds. It has been identified as being found in or released from six recorded sources, all of which are related to electrical and electronic equipment. These sources include antennas, cores yokes or armatures, discharge tubes with liquid pool cathodes, hybrid capacitors, and loudspeakers, along with one additional source.</description>
  <categories/>
  <types/>
  <synonyms>
    <synonym>(4R)-2,4,6-trimethyl-3,4-dihydropyridine-3,5-dicarboxylic acid diethyl ester</synonym>
    <synonym>1,4-Dihydro-2,4,6-trimethyl-3,5-pyridinedicarboxylic acid, diethyl ester</synonym>
    <synonym>1,4-Dihydro-3, 5-dicarbethoxycollidine</synonym>
    <synonym>1,4-Dihydro-3,5-dicarbethoxycollidine</synonym>
    <synonym>1H-imidazole, 2-ethyl-5-methyl-</synonym>
    <synonym>2,4,6-Trimethyl-1,4-dihydro-pyridine-3,5-dicarboxylic acid diethyl ester</synonym>
    <synonym>2758942</synonym>
    <synonym>3, 5-Diethoxycarbonyl-1,4-dihydrocollidine</synonym>
    <synonym>3,5-Bis(ethoxycarbonyl)-1, 4-dihydrocollidine</synonym>
    <synonym>3,5-Bis(ethoxycarbonyl)-1,4-dihydrocollidine</synonym>
    <synonym>3,5-Dicarbethoxy-1,4-dihydro-2,4,6-trimethylpyridine</synonym>
    <synonym>3,5-Dicarbethoxy-1,4-Dihydrocollidine</synonym>
    <synonym>3,5-Diethoxycarbonyl-1,4-dihydro-2,4,6-collidine</synonym>
    <synonym>3,5-Diethoxycarbonyl-1,4-Dihydro-2,4,6-Trimethylpyridine</synonym>
    <synonym>3,5-Diethoxycarbonyl-1,4-dihydro-s-collidine</synonym>
    <synonym>3,5-Diethoxycarbonyl-1,4-dihydrocollidine</synonym>
    <synonym>3,5-diethyl 2,4,6-trimethyl-1,4-dihydropyridine-3,5-dicarboxylate</synonym>
    <synonym>3,5-Pyridinedicarboxylic acid, 1,4-dihydro-2,4,6-trimethyl-, 3,5-diethyl ester</synonym>
    <synonym>3,5-Pyridinedicarboxylic acid, 1,4-dihydro-2,4,6-trimethyl-, diethyl ester</synonym>
    <synonym>3,5-Pyridinedicarboxylicacid, 1,4-dihydro-2,4,6-trimethyl-, 3,5-diethyl ester</synonym>
    <synonym>D003997</synonym>
    <synonym>DDC</synonym>
    <synonym>DDC (porphyrinogen)</synonym>
    <synonym>Dicarbethoxydihydrocollidine</synonym>
    <synonym>Diethoxycarbonyldihydrocollidine</synonym>
    <synonym>DIETHYL 1,4-DIHYDRO-2,4,6-TRIMETHYL-3,5-PYRIDINEDICARBOXYLATE</synonym>
    <synonym>diethyl 1,4-dihydro-2,4,6-trimethylpyridine-3,5-dicarboxylate</synonym>
    <synonym>Diethyl 2,4,6-trimethyl-1,4-dihydro-3,5-pyridinedicarboxylate</synonym>
    <synonym>Diethyl 2,4,6-trimethyl-1,4-dihydropyridine-3,5-dicarboxylate</synonym>
    <synonym>Diethyl-2,4,6-trimethyl-1,4-dihydropyridin-3,5-dicarboxylat</synonym>
    <synonym>ethyl 5-(ethoxycarbonyl)-2,4,6-trimethyl-1,4-dihydropyridine-3-carboxylate</synonym>
    <synonym>MFCD00005950</synonym>
    <synonym>TL8004408</synonym>
    <synonym>[632-93-9]</synonym>
  </synonyms>
  <chemical_formula>C14H21N1O4</chemical_formula>
  <average_molecular_weight>267.325</average_molecular_weight>
  <monisotopic_moleculate_weight>267.147058</monisotopic_moleculate_weight>
  <iupac_name>3,5-diethyl 2,4,6-trimethyl-1,4-dihydropyridine-3,5-dicarboxylate</iupac_name>
  <traditional_iupac>3,5-diethyl 2,4,6-trimethyl-1,4-dihydropyridine-3,5-dicarboxylate</traditional_iupac>
  <cas_registry_number>632-93-9</cas_registry_number>
  <smiles>CCOC(=O)C1=C(C)NC(C)=C(C1C)C(=O)OCC</smiles>
  <inchi>InChI=1S/C14H21NO4/c1-6-18-13(16)11-8(3)12(14(17)19-7-2)10(5)15-9(11)4/h8,15H,6-7H2,1-5H3</inchi>
  <inchikey>CDVAIHNNWWJFJW-UHFFFAOYSA-N</inchikey>
  <taxonomy>
    <kingdom>Organic compounds</kingdom>
    <super_class>Organoheterocyclic compounds</super_class>
    <class>Pyridines and derivatives</class>
    <sub_class>Hydropyridines</sub_class>
    <direct_parent>Dihydropyridinecarboxylic acids and derivatives</direct_parent>
    <alternate_parents>
      <alternative_parent>Amino acids and derivatives</alternative_parent>
      <alternative_parent>Azacyclic compounds</alternative_parent>
      <alternative_parent>Carbonyl compounds</alternative_parent>
      <alternative_parent>Dialkylamines</alternative_parent>
      <alternative_parent>Dicarboxylic acids and derivatives</alternative_parent>
      <alternative_parent>Enamines</alternative_parent>
      <alternative_parent>Enoate esters</alternative_parent>
      <alternative_parent>Hydrocarbon derivatives</alternative_parent>
      <alternative_parent>Organic oxides</alternative_parent>
      <alternative_parent>Organopnictogen compounds</alternative_parent>
      <alternative_parent>Vinylogous amides</alternative_parent>
    </alternate_parents>
    <substituents>
      <substituent>Aliphatic heteromonocyclic compound</substituent>
      <substituent>Alpha,beta-unsaturated carboxylic ester</substituent>
      <substituent>Amine</substituent>
      <substituent>Amino acid or derivatives</substituent>
      <substituent>Azacycle</substituent>
      <substituent>Carbonyl group</substituent>
      <substituent>Carboxylic acid derivative</substituent>
      <substituent>Carboxylic acid ester</substituent>
      <substituent>Dicarboxylic acid or derivatives</substituent>
      <substituent>Dihydropyridinecarboxylic acid derivative</substituent>
      <substituent>Enamine</substituent>
      <substituent>Enoate ester</substituent>
      <substituent>Hydrocarbon derivative</substituent>
      <substituent>Organic nitrogen compound</substituent>
      <substituent>Organic oxide</substituent>
      <substituent>Organic oxygen compound</substituent>
      <substituent>Organonitrogen compound</substituent>
      <substituent>Organooxygen compound</substituent>
      <substituent>Organopnictogen compound</substituent>
      <substituent>Secondary aliphatic amine</substituent>
      <substituent>Secondary amine</substituent>
      <substituent>Vinylogous amide</substituent>
    </substituents>
    <molecular_framework>Aliphatic heteromonocyclic compounds</molecular_framework>
    <descriptors>
      <descriptor>dihydropyridine</descriptor>
      <descriptor>ethyl ester</descriptor>
    </descriptors>
  </taxonomy>
  <status>Detected and Not Quantified</status>
  <origin/>
  <cellular_locations/>
  <biofluid_locations/>
  <tissue_locations/>
  <pathways/>
  <state/>
  <appearance/>
  <experimental_properties>
    <property>
      <kind>logp</kind>
      <value>2.2</value>
    </property>
  </experimental_properties>
  <predicted_properties>
    <property>
      <kind>logp</kind>
      <value>2.66</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>logs</kind>
      <value>-2.40</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>solubility</kind>
      <value>1.07e+00 g/l</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>logp</kind>
      <value>1.46</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>pka_strongest_acidic</kind>
      <value>19.6</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>pka_strongest_basic</kind>
      <value>-6.6</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>iupac</kind>
      <value>3,5-diethyl 2,4,6-trimethyl-1,4-dihydropyridine-3,5-dicarboxylate</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>average_mass</kind>
      <value>267.325</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>mono_mass</kind>
      <value>267.147058</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>smiles</kind>
      <value>CCOC(=O)C1=C(C)NC(C)=C(C1C)C(=O)OCC</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>formula</kind>
      <value>C14H21N1O4</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchi</kind>
      <value>InChI=1S/C14H21NO4/c1-6-18-13(16)11-8(3)12(14(17)19-7-2)10(5)15-9(11)4/h8,15H,6-7H2,1-5H3</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchikey</kind>
      <value>CDVAIHNNWWJFJW-UHFFFAOYSA-N</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>polar_surface_area</kind>
      <value>64.63</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>refractivity</kind>
      <value>74.24</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>polarizability</kind>
      <value>29.3</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>rotatable_bond_count</kind>
      <value>6</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>acceptor_count</kind>
      <value>3</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>donor_count</kind>
      <value>1</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>physiological_charge</kind>
      <value>0</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>formal_charge</kind>
      <value>0</value>
      <source>ChemAxon</source>
    </property>
  </predicted_properties>
  <route_of_exposure/>
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  <treatment/>
  <drugbank_id/>
  <hmdb_id/>
  <pubchem_compound_id>12446</pubchem_compound_id>
  <chembl_id/>
  <chemspider_id>11938</chemspider_id>
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  <general_references/>
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</compound>
