<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <version>1.0</version>
  <creation_date>2016-05-19 01:52:50 UTC</creation_date>
  <update_date>2026-08-22 12:22:35 UTC</update_date>
  <accession/>
  <common_name>ALBUMIN</common_name>
  <class>SmallMolecule</class>
  <description>ALBUMIN belongs to the organofluorides, a class of organohalogen compounds within the organic compounds. It has the chemical formula $\text{C}_3\text{F}_8$ and an average molecular weight of 188.02 g/mol.

In industrial applications, the compound serves several roles and uses. It is utilized as a thickening agent, a stabilizing agent, and a surfactant (surface active agent). It is further employed as a surface modifier, a flavouring and nutrient, and as processing aids not otherwise specified. Additionally, it is used as non-motive propellants, specifically as blowing agents.

ALBUMIN is found in or released from 50 recorded sources across multiple sectors. Within Electrical &amp; Electronic Equipment, it is associated with capacitors, cell phones, batteries, printed circuit boards, wires and cables, and 27 other items. In the sector of food, food processing &amp; cookware, it is linked to food packaging, food preservation, processing meats, processing fish, and the preparation of wine or sparkling wine. Household cleaning &amp; consumer products include soap detergents, bleaching agents, perfumes within detergents and soaps, tobacco smoke filters, and non electric simulated smoking devices. It is also found in synthetic textiles, carpets and rugs within the textiles, leather &amp; furnishings sector. Other sources include medical devices from the healthcare, pharmaceuticals &amp; veterinary products sector, as well as drinking water and water supply. Recorded exposure routes for the compound include touch, oral, and inhalation.</description>
  <categories/>
  <types>
    <type>Human Neurotoxin</type>
    <type>PFAS</type>
  </types>
  <synonyms/>
  <chemical_formula>C3F8</chemical_formula>
  <average_molecular_weight>188.0193</average_molecular_weight>
  <monisotopic_moleculate_weight>187.98722564</monisotopic_moleculate_weight>
  <iupac_name>octafluoropropane</iupac_name>
  <traditional_iupac>definity</traditional_iupac>
  <cas_registry_number>977005-72-3</cas_registry_number>
  <smiles>FC(F)(F)C(F)(F)C(F)(F)F</smiles>
  <inchi>InChI=1S/C3F8/c4-1(5,2(6,7)8)3(9,10)11</inchi>
  <inchikey>QYSGYZVSCZSLHT-UHFFFAOYSA-N</inchikey>
  <taxonomy>
    <kingdom>Organic compounds</kingdom>
    <super_class>Organohalogen compounds</super_class>
    <class>Organofluorides</class>
    <sub_class/>
    <direct_parent>Organofluorides</direct_parent>
    <alternate_parents>
      <alternative_parent>Alkyl fluorides</alternative_parent>
      <alternative_parent>Hydrocarbon derivatives</alternative_parent>
    </alternate_parents>
    <substituents>
      <substituent>Aliphatic acyclic compound</substituent>
      <substituent>Alkyl fluoride</substituent>
      <substituent>Alkyl halide</substituent>
      <substituent>Hydrocarbon derivative</substituent>
      <substituent>Organofluoride</substituent>
    </substituents>
    <molecular_framework>Aliphatic acyclic compounds</molecular_framework>
    <descriptors>
      <descriptor>fluorocarbon</descriptor>
    </descriptors>
  </taxonomy>
  <status>Detected and Not Quantified</status>
  <origin/>
  <cellular_locations/>
  <biofluid_locations/>
  <tissue_locations/>
  <pathways>
    <pathway>
      <name>Perflutren Metabolism</name>
      <smpdb_id>SMP0126933</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Perflutren Drug Metabolism Action Pathway</name>
      <smpdb_id>SMP0143005</smpdb_id>
      <kegg_map_id/>
    </pathway>
  </pathways>
  <state/>
  <appearance/>
  <experimental_properties>
    <property>
      <kind>logp</kind>
      <value>3.1</value>
    </property>
  </experimental_properties>
  <predicted_properties>
    <property>
      <kind>logp</kind>
      <value>2.96</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>logs</kind>
      <value>-3.11</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>solubility</kind>
      <value>1.46e-01 g/l</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>logp</kind>
      <value>2.78</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>iupac</kind>
      <value>octafluoropropane</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>average_mass</kind>
      <value>188.0193</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>mono_mass</kind>
      <value>187.98722564</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>smiles</kind>
      <value>FC(F)(F)C(F)(F)C(F)(F)F</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>formula</kind>
      <value>C3F8</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchi</kind>
      <value>InChI=1S/C3F8/c4-1(5,2(6,7)8)3(9,10)11</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchikey</kind>
      <value>QYSGYZVSCZSLHT-UHFFFAOYSA-N</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>polar_surface_area</kind>
      <value>0</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>refractivity</kind>
      <value>17.54</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>polarizability</kind>
      <value>7.1</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>rotatable_bond_count</kind>
      <value>2</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>acceptor_count</kind>
      <value>0</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>donor_count</kind>
      <value>0</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/>
  <mechanism_of_toxicity/>
  <metabolism/>
  <toxicity/>
  <lethaldose/>
  <carcinogenicity/>
  <use_source/>
  <min_risk_level/>
  <health_effects>#&lt;HealthEffect::ActiveRecord_Associations_CollectionProxy:0x00007f722456c640&gt;</health_effects>
  <symptoms/>
  <treatment/>
  <drugbank_id>DB00556</drugbank_id>
  <hmdb_id/>
  <pubchem_compound_id>6432</pubchem_compound_id>
  <chembl_id/>
  <chemspider_id>6192</chemspider_id>
  <kegg_id/>
  <uniprot_id/>
  <omim_id/>
  <chebi_id/>
  <biocyc_id/>
  <ctd_id/>
  <stitch_id/>
  <actor_id/>
  <pdb_id/>
  <wikipidia/>
  <general_references/>
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</compound>
