{"Abbreviation":"4-MBZP","Aliases":["1-(4-Methylbenzyl)piperazine","625-263-4","Piperazine,1-[(4-methylphenyl)methyl]-","[(4-methylphenyl)methyl]piperazine","1-(4-methylbenzyl)-piperazine","1-(4-Methyl-benzyl)-piperazine","Bas 01375866","(4-methylbenzyl)piperazine","1-(p-tolylmethyl)piperazine","N-(4-methylbenzyl)piperazine","4-(4-methylbenzyl)piperazine","SBB003648","STK299975","1-(4-Methylbenzyl)piperazine, 97%","FS-1577","ST45091546","En300-131927","F16014","A816611","Z228580292","1-(p-tolylmethyl)piperazine;1-(4-Methylbenzyl)-piperazine"],"CAS":"23173-57-1","ChemicalClasses":["benzylpiperazine"],"Chirality":"achiral","Classes":["Stimulant"],"Erowid Experience Reports":null,"Esters":[],"European Community (EC) Number":"625-263-4","Formating":[],"HeavyAtomCount":14,"IUPACName":"1-[(4-methylphenyl)methyl]piperazine","InChI":"InChI=1S/C12H18N2/c1-11-2-4-12(5-3-11)10-14-8-6-13-7-9-14/h2-5,13H,6-10H2,1H3","InChIKey":"RNAXUUAJNMDESG-UHFFFAOYSA-N","MolecularFormula":"C\u003csub\u003e12\u003c/sub\u003eH\u003csub\u003e18\u003c/sub\u003eN\u003csub\u003e2\u003c/sub\u003e","MolecularWeight":"190.28 g/mol","PubChemId":764723,"RefCount":2,"RefCur":"","References":[{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/764723","Name":"4-Methylbenzylpiperazine","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=23173-57-1","Name":"4-Methylbenzylpiperazine","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID60945847","Name":"4-Methylbenzylpiperazine","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 764723, 4-Methylbenzylpiperazine. Accessed July 18, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/764723\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/764723\u003c/a\u003e"],"SMILES":"CC1=CC=C(C=C1)CN2CCNCC2","SaltData":[],"Salts":[],"StereoisomerData":[],"Stereoisomers":[],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 100.181 32.556\"\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 0h101v33H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m1.038 31.51 13.191-7.616\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.224 8.654.005 15.24M16.663 10.062l.004 12.424\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.224 8.654 13.191-7.616\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M40.611 8.662 27.415 1.038M38.173 10.07 27.415 3.854\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.611 8.662.005 15.24\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.425 31.518 13.191-7.616M27.425 28.702l10.752-6.207\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.229 23.894 13.196 7.624M40.611 8.662l13.191-7.615M53.802 1.047l10.037 5.795M66.991 12.512l-.003 11.39M66.988 23.902l13.191 7.616M80.179 31.518l10.042-5.802M93.376 20.044l.003-11.39M93.379 8.654 80.188 1.038M70.146 6.841l10.042-5.803\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"M68.933 11.112h-.72l-2.619-4.066h-.03l.03.595q.024.358.024.733v2.738h-.566V6.213h.714l2.608 4.054h.03l-.018-.328-.024-.476q-.006-.262-.006-.482V6.213h.577z\" class=\"atom\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M95.315 26.344h-.72l-2.62-4.066h-.029l.029.595q.024.357.024.732v2.739h-.565v-4.9h.714l2.608 4.054h.029l-.017-.327-.024-.476q-.006-.262-.006-.483v-2.768h.577zM99.621 26.344h-.619v-2.286H96.49v2.286h-.613v-4.9h.613v2.072h2.512v-2.072h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#3050f8\" d=\"M63.839 6.842 58.82 3.944M66.991 12.512l-.002 5.695M90.221 25.716 85.2 28.617M93.376 20.044l.001-5.695M70.146 6.841l5.021-2.901\" 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":"4-Methylbenzylpiperazine","XLogP":1.5}