Jump to content

N-Methylclonazepam

From Wikipedia, the free encyclopedia
(Redirected from Ro05-4082)

N-Methylclonazepam
Legal status
Legal status
Identifiers
  • 5-(2-chlorophenyl)-1-methyl-7-nitro-3H-1,4-benzodiazepin-2-one
CAS Number
PubChem CID
UNII
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC16H12ClN3O3
Molar mass329.74 g·mol−1
3D model (JSmol)
  • CN1C(=O)CN=C(C2=C1C=CC(=C2)[N+](=O)[O-])C3=CC=CC=C3Cl
  • InChI=1S/C16H12ClN3O3/c1-19-14-7-6-10(20(22)23)8-12(14)16(18-9-15(19)21)11-4-2-3-5-13(11)17/h2-8H,9H2,1H3
  • Key:AZVBJJDUDXZLTM-UHFFFAOYSA-N

N-Methylclonazepam (also known as Ro05-4082, ID-690 and methylclonazepam)[1] is a benzodiazepine derivative developed in the 1970s. It has sedative and hypnotic properties, and has around the same potency as clonazepam itself.[2] It was never introduced into clinical use. It is a structural isomer of meclonazepam (3-methylclonazepam), and similarly has been sold as a designer drug, first being identified in Sweden in 2017.[3]

In July 2025, N-methylclonazepam was identified alongside fentanyl as a component in a batch of drugs linked to a mass overdose in Baltimore, Maryland.[4][5] There were at least 27 hospitalisations, and many patients remained unconscious even after administration of naloxone; a NIST research chemist said this may have been due to the sedative effects of the methylclonazepam.[4]

See also

[edit]

References

[edit]
  1. ↑ "UNII - 89WG8CN9AJ | UNII Search Service". precision.fda.gov. Retrieved 4 May 2026.
  2. ↑ Fukuda H, Kudo Y, Ono H, Togari A, Tanaka Y (January 1977). "[Pharmacological study on 5-(o-chlorophenyl)-1-methyl-7-nitro-1,3-dihydro-2H-1,4-benzodiazepin-2-one (ID-690), with special reference to the effects on motor systems]". Nihon Yakurigaku Zasshi. Folia Pharmacologica Japonica (in Japanese). 73 (1): 123–134. doi:10.1254/fpj.73.123. PMID 558942.
  3. ↑ "Novel Benzodiazepines. A review of the evidence of use and harms of Novel Benzodiazepines" (PDF). Advisory Council on the Misuse of Drugs. April 2020.
  4. 1 2 Cohn M, Zhu A, Sanderlin LO (17 July 2025). "Fentanyl mixed with a new illicit drug may be to blame for mass overdose". The Banner. Retrieved 4 May 2026.
  5. ↑ Kiefer P (19 July 2025). "Baltimore overdoses may be linked to new drug". The Washington Post. ISSN 0190-8286. Retrieved 4 May 2026.