Record Information
Version1.0
Creation Date2014-08-30 21:04:37 UTC
Update Date2026-05-14 17:01:51 UTC
Accession NumberCHEM003522
Identification
Common NameHeroin
ClassSmall Molecule
DescriptionA narcotic analgesic that may be habit-forming. It is a controlled substance (opium derivative) listed in the U.S. Code of Federal Regulations, Title 21 Parts 329.1, 1308.11 (1987). Sale is forbidden in the United States by Federal statute. (Merck Index, 11th ed) Internationally, heroin is controlled under Schedules I and IV of the Single Convention on Narcotic Drugs. It is illegal to manufacture, possess, or sell heroin in the United States and the UK. However, under the name diamorphine, heroin is a legal prescription drug in the United Kingdom.
Contaminant Sources
  • STOFF IDENT Compounds
  • T3DB toxins
  • ToxCast & Tox21 Chemicals
Contaminant Type
  • Amine
  • Analgesic, Opioid
  • Drug
  • Ester
  • Ether
  • Narcotic
  • Organic Compound
  • Synthetic Compound
Chemical Structure
Thumb
Synonyms
ValueSource
(5alpha,6alpha)-7,8-Didehydro-4,5-epoxy-17-methylmorphinan-3,6-diol diacetate (ester)ChEBI
3,6-DiacetylmorphineChEBI
7,8-Dihydro-4,5-alpha-epoxy-17-methylmorphinan-3,6-alpha-diol diacetateChEBI
DiacetylmorphineChEBI
DiamorphineChEBI
O,O'-diacetylmorphineChEBI
(5a,6a)-7,8-Didehydro-4,5-epoxy-17-methylmorphinan-3,6-diol diacetate (ester)Generator
(5a,6a)-7,8-Didehydro-4,5-epoxy-17-methylmorphinan-3,6-diol diacetic acid (ester)Generator
(5alpha,6alpha)-7,8-Didehydro-4,5-epoxy-17-methylmorphinan-3,6-diol diacetic acid (ester)Generator
(5Α,6α)-7,8-didehydro-4,5-epoxy-17-methylmorphinan-3,6-diol diacetate (ester)Generator
(5Α,6α)-7,8-didehydro-4,5-epoxy-17-methylmorphinan-3,6-diol diacetic acid (ester)Generator
7,8-Dihydro-4,5-a-epoxy-17-methylmorphinan-3,6-a-diol diacetateGenerator
7,8-Dihydro-4,5-a-epoxy-17-methylmorphinan-3,6-a-diol diacetic acidGenerator
7,8-Dihydro-4,5-alpha-epoxy-17-methylmorphinan-3,6-alpha-diol diacetic acidGenerator
7,8-Dihydro-4,5-α-epoxy-17-methylmorphinan-3,6-α-diol diacetateGenerator
7,8-Dihydro-4,5-α-epoxy-17-methylmorphinan-3,6-α-diol diacetic acidGenerator
Hydrochloride, diacetylmorphineMeSH
Min-I-jet morphine sulphateMeSH
DiagesilMeSH
DiamorfMeSH
Heroin hydrochlorideMeSH
Diacetylmorphine hydrochlorideMeSH
Hydrochloride, heroinMeSH
Min I jet morphine sulphateMeSH
Evans vaccines brand OF heroin hydrochlorideMeSH
APS brand OF heroin hydrochlorideMeSH
Chemical FormulaC21H23NO5
Average Molecular Mass369.411 g/mol
Monoisotopic Mass369.158 g/mol
CAS Registry Number561-27-3
IUPAC Name(1S,5R,13R,14S,17R)-10-(acetyloxy)-4-methyl-12-oxa-4-azapentacyclo[9.6.1.0^{1,13}.0^{5,17}.0^{7,18}]octadeca-7(18),8,10,15-tetraen-14-yl acetate
Traditional Name(1S,5R,13R,14S,17R)-14-(acetyloxy)-4-methyl-12-oxa-4-azapentacyclo[9.6.1.0¹,¹³.0⁵,¹⁷.0⁷,¹⁸]octadeca-7(18),8,10,15-tetraen-10-yl acetate
SMILES[H][C@@]12OC3=C(OC(C)=O)C=CC4=C3[C@@]11CCN(C)[C@]([H])(C4)[C@]1([H])C=C[C@@H]2OC(C)=O
InChI IdentifierInChI=1S/C21H23NO5/c1-11(23)25-16-6-4-13-10-15-14-5-7-17(26-12(2)24)20-21(14,8-9-22(15)3)18(13)19(16)27-20/h4-7,14-15,17,20H,8-10H2,1-3H3/t14-,15+,17-,20-,21-/m0/s1
InChI KeyGVGLGOZIDCSQPN-PVHGPHFFSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as morphinans. These are polycyclic compounds with a four-ring skeleton with three condensed six-member rings forming a partially hydrogenated phenanthrene moiety, one of which is aromatic while the two others are alicyclic.
KingdomOrganic compounds
Super ClassAlkaloids and derivatives
ClassMorphinans
Sub ClassNot Available
Direct ParentMorphinans
Alternative Parents
Substituents
  • Morphinan
  • Phenanthrene
  • Tetralin
  • Coumaran
  • Alkyl aryl ether
  • Aralkylamine
  • Dicarboxylic acid or derivatives
  • Piperidine
  • Benzenoid
  • Amino acid or derivatives
  • Carboxylic acid ester
  • Tertiary amine
  • Tertiary aliphatic amine
  • Ether
  • Carboxylic acid derivative
  • Oxacycle
  • Azacycle
  • Organoheterocyclic compound
  • Organic nitrogen compound
  • Hydrocarbon derivative
  • Organic oxide
  • Organooxygen compound
  • Organonitrogen compound
  • Organopnictogen compound
  • Organic oxygen compound
  • Amine
  • Carbonyl group
  • Aromatic heteropolycyclic compound
Molecular FrameworkAromatic heteropolycyclic compounds
External Descriptors
Biological Properties
StatusDetected and Not Quantified
OriginExogenous
Cellular Locations
  • Cytoplasm
  • Extracellular
Biofluid LocationsNot Available
Tissue LocationsNot Available
PathwaysNot Available
Applications
Biological Roles
Chemical RolesNot Available
Physical Properties
StateSolid
AppearanceWhite powder.
Experimental Properties
PropertyValue
Melting Point173 °C
Boiling Point272-274 °C at 1.20E+01 mm Hg
Solubility600 mg/L (at 25 °C)
Predicted Properties
PropertyValueSource
Water Solubility0.27 g/LALOGPS
logP2.3ALOGPS
logP1.55ChemAxon
logS-3.1ALOGPS
pKa (Strongest Basic)9.1ChemAxon
Physiological Charge1ChemAxon
Hydrogen Acceptor Count4ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area65.07 ŲChemAxon
Rotatable Bond Count4ChemAxon
Refractivity98.43 m³·mol⁻¹ChemAxon
Polarizability37.9 ųChemAxon
Number of Rings5ChemAxon
Bioavailability1ChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Spectra
Spectra
Spectrum TypeDescriptionSplash KeyView
Predicted GC-MSPredicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positivesplash10-016u-2079000000-b1a98da90b10b2f6fb14Spectrum
LC-MS/MSLC-MS/MS Spectrum - LC-ESI-QTOF , positivesplash10-00di-0009000000-43bbf64aafa84c20e09cSpectrum
LC-MS/MSLC-MS/MS Spectrum - LC-ESI-QTOF , positivesplash10-00di-0009000000-d35dead9831fb810a273Spectrum
LC-MS/MSLC-MS/MS Spectrum - LC-ESI-QTOF , positivesplash10-00di-0039000000-3824b8beec641e65acedSpectrum
LC-MS/MSLC-MS/MS Spectrum - LC-ESI-QTOF , positivesplash10-0303-0593000000-b8c7c4e8760df849eeb2Spectrum
LC-MS/MSLC-MS/MS Spectrum - LC-ESI-QTOF , positivesplash10-014l-0950000000-9cd1cf455c3a42888ee6Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-024i-0029000000-621a646ce875dfe29a86Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-03fr-1049000000-914d38bbfbcc120deba5Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-014i-2091000000-4af238bd53e55b1a2237Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-00or-2009000000-c77b2701df5a4dd2f03bSpectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-05r0-3029000000-ac3b8b35c5f87a9db00bSpectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0a4i-9052000000-69d8cee7b68a147f5c7fSpectrum
MSMass Spectrum (Electron Ionization)splash10-016u-5955000000-17dd3ef75849a9fb63c3Spectrum
Toxicity Profile
Route of ExposureBioavailability is less than 35%.
Mechanism of ToxicityHeroin is a mu-opioid agonist. It acts on endogenous mu-opioid receptors that are spread in discrete packets throughout the brain, spinal cord and gut in almost all mammals. Heroin, along with other opioids, are agonists to four endogenous neurotransmitters. They are beta-endorphin, dynorphin, leu-enkephalin, and met-enkephalin. The body responds to heroin in the brain by reducing (and sometimes stopping) production of the endogenous opioids when heroin is present. Endorphins are regularly released in the brain and nerves, attenuating pain. Their other functions are still obscure, but are probably related to the effects produced by heroin besides analgesia (antitussin, anti-diarrheal).
MetabolismHepatic. Route of Elimination: 90% renal as glucuronides, rest biliary Half Life: <10 minutes
Toxicity ValuesNot Available
Lethal DoseNot Available
Carcinogenicity (IARC Classification)No indication of carcinogenicity to humans (not listed by IARC).
Uses/SourcesUsed in the treatment of acute pain, myocardial infarction, acute pulmonary oedema, and chronic pain.
Minimum Risk LevelNot Available
Health EffectsNot Available
SymptomsNot Available
TreatmentNot Available
Concentrations
Not Available
DrugBank IDDB01452
HMDB IDHMDB0061331
FooDB IDNot Available
Phenol Explorer IDNot Available
KNApSAcK IDNot Available
BiGG IDNot Available
BioCyc IDNot Available
METLIN IDNot Available
PDB IDNot Available
Wikipedia LinkHeroin
Chemspider ID4575379
ChEBI ID27808
PubChem Compound ID5462328
Kegg Compound IDC06534
YMDB IDNot Available
ECMDB IDNot Available
References
Synthesis ReferenceNot Available
MSDSNot Available
General References
1. https://www.ncbi.nlm.nih.gov/pubmed/?term=10454516
2. https://www.ncbi.nlm.nih.gov/pubmed/?term=11441925
3. https://www.ncbi.nlm.nih.gov/pubmed/?term=11448454
4. https://www.ncbi.nlm.nih.gov/pubmed/?term=11557911
5. https://www.ncbi.nlm.nih.gov/pubmed/?term=12965116
6. https://www.ncbi.nlm.nih.gov/pubmed/?term=14534521
7. https://www.ncbi.nlm.nih.gov/pubmed/?term=15212982
8. https://www.ncbi.nlm.nih.gov/pubmed/?term=15213301
9. https://www.ncbi.nlm.nih.gov/pubmed/?term=15550572
10. https://www.ncbi.nlm.nih.gov/pubmed/?term=15772255
11. https://www.ncbi.nlm.nih.gov/pubmed/?term=15843500
12. https://www.ncbi.nlm.nih.gov/pubmed/?term=16076083
13. https://www.ncbi.nlm.nih.gov/pubmed/?term=16333714
14. https://www.ncbi.nlm.nih.gov/pubmed/?term=20331562
15. https://www.ncbi.nlm.nih.gov/pubmed/?term=20649590
16. https://www.ncbi.nlm.nih.gov/pubmed/?term=20735218
17. https://www.ncbi.nlm.nih.gov/pubmed/?term=20810225
18. https://www.ncbi.nlm.nih.gov/pubmed/?term=20855171
19. https://www.ncbi.nlm.nih.gov/pubmed/?term=21235340
20. https://www.ncbi.nlm.nih.gov/pubmed/?term=21309955
21. https://www.ncbi.nlm.nih.gov/pubmed/?term=21362452
22. https://www.ncbi.nlm.nih.gov/pubmed/?term=21452028
23. https://www.ncbi.nlm.nih.gov/pubmed/?term=21527184
24. https://www.ncbi.nlm.nih.gov/pubmed/?term=21568984
25. https://www.ncbi.nlm.nih.gov/pubmed/?term=21608377
26. https://www.ncbi.nlm.nih.gov/pubmed/?term=21734607
27. https://www.ncbi.nlm.nih.gov/pubmed/?term=21740578
28. https://www.ncbi.nlm.nih.gov/pubmed/?term=2352148
29. https://www.ncbi.nlm.nih.gov/pubmed/?term=8858977
30. https://www.ncbi.nlm.nih.gov/pubmed/?term=8893832
31. https://www.ncbi.nlm.nih.gov/pubmed/?term=9918543