{"Abbreviation":["2-BZP"],"Aliases":["2-Benzylpiperazine","Dtxsid90339831","Dtxcid30290912","2-Benzyl-piperazine","Mfcd07367777","3-benzyl-piperazine","2-phenylmethylpiperazine","2-(phenylmethyl)-piperazine","2-BZP","Schembl16738","Schembl72389","Schembl2465336","Schembl4078970","Schembl28403845","2-(Phenylmethyl)piperazine","Akos005255251","AB31245","AB36528","AB36531","FB151256","HY-60174","DB-062810","DB-066357","DB-076043","CS-0005366","En300-242045","F600287"],"CAS":"84477-71-4","ChemicalClasses":["amphetamine"],"Chirality":"racemic","Classes":["Stimulant"],"Esters":[],"European Community (EC) Number":"804-666-0","Formating":[],"HeavyAtomCount":13,"IUPACName":"2-benzylpiperazine","InChI":"InChI=1S/C11H16N2/c1-2-4-10(5-3-1)8-11-9-12-6-7-13-11/h1-5,11-13H,6-9H2","InChIKey":"RITMXTLCKYLIKW-UHFFFAOYSA-N","MeSH Headers":[],"MolecularFormula":"C\u003csub\u003e11\u003c/sub\u003eH\u003csub\u003e16\u003c/sub\u003eN\u003csub\u003e2\u003c/sub\u003e","MolecularWeight":"176.26 g/mol","PD":"PD077073","PubChemId":559033,"RefChem":"256623","RefCount":2,"RefCur":"","References":[{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q72442713","Name":"2-Benzylpiperazine","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/559033","Name":"2-Benzylpiperazine","Sub":false}]},{"Name":"Probes \u0026 Drugs","Urls":[{"Link":"https://www.probes-drugs.org/compound/PD077073","Name":"2-Benzylpiperazine","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=84477-71-4","Name":"2-Benzylpiperazine","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID90339831","Name":"2-Benzylpiperazine","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 559033, 2-Benzylpiperazine. Accessed April 29, 2026. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/559033\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/559033\u003c/a\u003e"],"SMILES":"C1CNC(CN1)CC2=CC=CC=C2","SaltData":[],"Salts":[],"StereoisomerData":[{"ChemicalClasses":["amphetamine"],"SMILES":"C1=CC=C(C[C@H]2CNCCN2)C=C1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 81.249 47.405\"\u003e\u003crect width=\"100%\" height=\"100%\" fill=\"#fff\"/\u003e\u003cdesc\u003eGenerated by the Chemistry Development Kit (http://github.com/cdk)\u003c/desc\u003e\u003cg fill=\"#3050f8\" stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h82v48H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 16.08.005 15.24M3.477 17.488l.004 12.425\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.038 16.08 13.191-7.616\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M27.425 16.089 14.229 8.464M24.987 17.496 14.229 11.28\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.425 16.089 13.191-7.616\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m53.504 16.264.606-.35M51.052 15.14l1.112-.641M48.601 14.017l1.617-.934M46.15 12.893l2.122-1.225M43.699 11.77l2.627-1.517M41.248 10.646l3.132-1.808M38.797 9.523l3.638-2.1\"/\u003e\u003c/g\u003e\u003cpath d=\"m53.807 16.089.002 15.231M53.809 31.32l10.048 5.795M70.164 37.114l10.046-5.798M80.21 31.316l-.002-15.232M80.208 16.084 70.16 10.29M53.807 16.089l10.046-5.798M27.425 16.089l.005 15.24\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.239 38.944 13.191-7.615M14.239 36.129l10.752-6.208\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.043 31.32 13.196 7.624\" class=\"bond\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.952 41.384h-.721l-2.619-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.715l2.607 4.054h.03l-.018-.327-.024-.476q-.006-.262-.006-.483v-2.768h.578zM68.815 46.845h-.619v-2.286h-2.513v2.286h-.613v-4.9h.613v2.072h2.513v-2.072h.619z\"/\u003e\u003c/g\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.947 10.921h-.721l-2.619-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.715l2.607 4.054h.03l-.018-.327-.024-.476q-.006-.262-.006-.483V6.021h.578zM68.81 5.459h-.619V3.173h-2.512v2.286h-.614V.56h.614v2.072h2.512V.56h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#3050f8\" d=\"m63.857 37.115-5.024-2.897M70.164 37.114l5.023-2.899M70.16 10.29l5.024 2.897M70.16 10.29l5.024 2.897M63.853 10.291 58.83 13.19M63.853 10.291 58.83 13.19\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(S)-2-Benzylpiperazine"},{"ChemicalClasses":["amphetamine"],"SMILES":"C1=CC=C(C[C@@H]2CNCCN2)C=C1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 81.249 47.405\"\u003e\u003crect width=\"100%\" height=\"100%\" fill=\"#fff\"/\u003e\u003cdesc\u003eGenerated by the Chemistry Development Kit (http://github.com/cdk)\u003c/desc\u003e\u003cg fill=\"#3050f8\" stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h82v48H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 16.08.005 15.24M3.477 17.488l.004 12.425\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.038 16.08 13.191-7.616\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M27.425 16.089 14.229 8.464M24.987 17.496 14.229 11.28\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.425 16.089 13.191-7.616\" class=\"bond\"/\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"m53.632 16.392.35-.606-11.747-8.652-1.969 1.137-2.25 1.299z\" class=\"bond\"/\u003e\u003cpath d=\"m53.807 16.089.002 15.231M53.809 31.32l10.048 5.795M70.164 37.114l10.046-5.798M80.21 31.316l-.002-15.232M80.208 16.084 70.16 10.29M53.807 16.089l10.046-5.798M27.425 16.089l.005 15.24\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.239 38.944 13.191-7.615M14.239 36.129l10.752-6.208\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.043 31.32 13.196 7.624\" class=\"bond\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.952 41.384h-.721l-2.619-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.715l2.607 4.054h.03l-.018-.327-.024-.476q-.006-.262-.006-.483v-2.768h.578zM68.815 46.845h-.619v-2.286h-2.513v2.286h-.613v-4.9h.613v2.072h2.513v-2.072h.619z\"/\u003e\u003c/g\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.947 10.921h-.721l-2.619-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.715l2.607 4.054h.03l-.018-.327-.024-.476q-.006-.262-.006-.483V6.021h.578zM68.81 5.459h-.619V3.173h-2.512v2.286h-.614V.56h.614v2.072h2.512V.56h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#3050f8\" d=\"m63.857 37.115-5.024-2.897M70.164 37.114l5.023-2.899M70.16 10.29l5.024 2.897M70.16 10.29l5.024 2.897M63.853 10.291 58.83 13.19M63.853 10.291 58.83 13.19\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(R)-2-Benzylpiperazine"}],"StereoisomerType":"enantiomer","Stereoisomers":["(S)-2-Benzylpiperazine","(R)-2-Benzylpiperazine"],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 81.249 47.405\"\u003e\u003crect width=\"100%\" height=\"100%\" fill=\"#fff\"/\u003e\u003cdesc\u003eGenerated by the Chemistry Development Kit (http://github.com/cdk)\u003c/desc\u003e\u003cg fill=\"#3050f8\" stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h82v48H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m80.21 31.316-.002-15.232M80.208 16.084 70.16 10.29M63.853 10.291l-10.046 5.798M53.807 16.089l.002 15.231M53.809 31.32l10.048 5.795M80.21 31.316l-10.046 5.798M53.807 16.089 40.616 8.473M40.616 8.473l-13.191 7.616\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M27.425 16.089 14.229 8.464M24.987 17.496 14.229 11.28\"/\u003e\u003c/g\u003e\u003cpath d=\"M14.229 8.464 1.038 16.08\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 16.08.005 15.24M3.477 17.488l.004 12.425\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.043 31.32 13.196 7.624\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.239 38.944 13.191-7.615M14.239 36.129l10.752-6.208\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.425 16.089.005 15.24\" class=\"bond\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.947 10.921h-.721l-2.619-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.715l2.607 4.054h.03l-.018-.327-.024-.476q-.006-.262-.006-.483V6.021h.578zM68.81 5.459h-.619V3.173h-2.512v2.286h-.614V.56h.614v2.072h2.512V.56h.619z\"/\u003e\u003c/g\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.952 41.384h-.721l-2.619-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.715l2.607 4.054h.03l-.018-.327-.024-.476q-.006-.262-.006-.483v-2.768h.578zM68.815 46.845h-.619v-2.286h-2.513v2.286h-.613v-4.9h.613v2.072h2.513v-2.072h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#3050f8\" d=\"m70.16 10.29 5.024 2.897M70.16 10.29l5.024 2.897M63.853 10.291 58.83 13.19M63.853 10.291 58.83 13.19M63.857 37.115l-5.024-2.897M70.164 37.114l5.023-2.899\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Subjective Effects":{"Cognitive Effects":["Analysis enhancement","Ego inflation","Focus enhancement","Increased music appreciation","Motivation enhancement","Thought acceleration","Wakefulness","Disinhibition","Suggestibility suppression","Cognitive euphoria","Compulsive redosing","Mania"],"Physical Effects":["Increased libido","Stamina enhancement","Stimulation","Appetite suppression","Dehydration","Dry mouth","Restless legs","Shakiness","Teeth grinding","Abnormal heartbeat","Increased blood pressure","Increased heart rate","Vasoconstriction"],"Visual Effects":[]},"Title":"2-Benzylpiperazine","Wikidata":"Q72442713","XLogP":1.2}