chembox verifiedrevid 399927651 ImageFile1 F 22 psychedelic .png ImageSize1 200px ImageFile2 ImageSize2 200px IUPACName 2 5 Methoxy 2,2 dimethyl 2,3 dihydro benzofuran 6 yl 1 methyl ethylamine OtherNames 6 2 Aminopropyl 5 methoxy 2,2 dimethyl 2,3 dihydrobenzofuran Section1 Chembox Identifiers ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 13180083 InChI 1 C14H21NO2 c1 9 15 5 10 6 13 11 7 12 10 16 4 8 14 2,3 17 13 h6 7,9H,5,8,15H2,1 4H3 InChIKey ZUGGTXPIKSRFHP UHFFFAOYAN SMILES1 O c2cc1c OC C1 C C cc2CC N C C StdInChI Ref stdinchicite correct chemspider StdInChI 1S C14H21NO2 c1 9 15 5 10 6 13 11 7 12 10 16 4 8 14 2,3 17 13 h6 7,9H,5,8,15H2,1 4H3 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey ZUGGTXPIKSRFHP UHFFFAOYSA N CASNo 952016 51 2 PubChem 16051705 SMILES C1 C2C CC C1CC C N OC CC O2 C C Section2 Chembox Properties Formula C sub 14 sub H sub 21 sub NO sub 2 sub MolarMass 235.325 g mol Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition F 22 , or 6 2 amino propyl 5 methoxy 2,2 di methyl 2,3 dihydro benzofuran , is a lesser known Psychedelics, dissociatives and deliriants psychedelic drug . F 22 was first synthesized by Alexander Shulgin . In his book PiHKAL PiHKAL Phenethylamines i Have Known And Loved , the minimum dosage is listed as 15 mg, and the duration unknown. F 22 produces few to no effects. Very little data exists about the pharmacological properties, metabolism, and toxicity of F 22. See also Phenethylamine Psychedelics, dissociatives and deliriants External links http www.erowid.org library books online pihkal pihkal080.shtml F 22 Entry in PiHKAL http pihkal.info read.php?domain pk&id 80 F 22 Entry in PiHKAL info PiHKAL Category Psychedelic phenethylamines Category Benzofurans Category Phenol ethers Psychoactive stub fa ... more details
chembox verifiedrevid 400869643 ImageFile Propynyl psychedelic .png ImageSize IUPACName 2 3,5 dimethoxy 4 prop 2 yn 1 yloxy phenyl ethanamine OtherNames Section1 Chembox Identifiers InChI 1 C13H17NO3 c1 4 7 17 13 11 15 2 8 10 5 6 14 9 12 13 16 3 h1,8 9H,5 7,14H2,2 3H3 InChIKey KNIWBMMJSJHUJB UHFFFAOYAM StdInChI Ref stdinchicite correct chemspider StdInChI 1S C13H17NO3 c1 4 7 17 13 11 15 2 8 10 5 6 14 9 12 13 16 3 h1,8 9H,5 7,14H2,2 3H3 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey KNIWBMMJSJHUJB UHFFFAOYSA N CASNo 952017 05 9 ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 21106371 PubChem SMILES COc1cc cc OC c1OCC C CCN Section2 Chembox Properties Formula C sub 13 sub H sub 17 sub NO sub 3 sub MolarMass 235.279 g mol Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition Propynyl , or 4 propynyl oxy 3,5 di methoxy phenethylamine , is a lesser known Psychedelics, dissociatives and deliriants psychedelic drug . It is closely related in structure to mescaline . Propynyl was first synthesized by Alexander Shulgin . In his book PiHKAL PiHKAL Phenethylamines i Have Known And Loved , the minimum dosage is listed as 80 mg, and the duration listed as 8 12 hours. Propynyl produces a body load and few to no mental effects. Very little data exists about the pharmacological properties, metabolism, and toxicity of propynyl. See also Phenethylamine Psychedelics, dissociatives and deliriants External links http www.erowid.org library books online pihkal pihkal143.shtml Propynyl entry in PiHKAL http pihkal.info read.php?domain pk&id 143 Propynyl entry in PiHKAL info PiHKAL Category Psychedelic phenethylamines Psychoactive stub fa ... more details
Infobox Hollywood cartoon cartoon name Psychedelic Pink series Pink Panther character Pink Panther image Pshypink TITLE.JPEG caption director Hawley Pratt animator Bob Matz br Warren Batchelder br Don Williams animator Don Williams br Manny Gould br Manny Perez animator Manny Perez background artist Tom O Loughlin musician Walter Greene producer David H. DePatie br Friz Freleng distributor United Artists release date Flag icon US February 21, 1968 in film 1968 color process DeLuxe Color Deluxe runtime 6 17 country USA movie language English language English preceded by Pinkadilly Circus followed by Come On In The Water s Pink Psychedelic Pink is the 39th cartoon produced in the Pink Panther series. A total of 124 6 minute cartoons were produced between 1964 and 1980. In this episode, Pink goes to a magical library with a weird eye on the entrance door. Laugh track The Pink Panther Show contained a laugh track when the Pink Panther cartoons were broadcast on NBC TV. When MGM released all 124 Pink Panther cartoons on DVD in 2006, the theatrical versions were, for the most part, utilized. However, several television prints made their way onto the DVD set, Psychedelic Pink being one of them. As a result, the laugh tracked version is currently available. ref name imdbShock Cite book last Alvin81 first authorlink coauthors title Review plot summary written by Oanabay04 as Alvin81 for imdb.com publisher date 2006 location pages url http www.imdb.com title tt0059713 comment doi id isbn ref References Reflist Further sources Meet the Pink Panther by Hope Freleng and Sybil Freleng http www.amazon.com dp 0789313081 , Universe Publishing, 2005 . The Pink Panther Classic Cartoon Collection http www.amazon.com dp B0009S4J2I 2006 . DVD set . New York MGM Home Video. http dfe.goldenagecartoons.com DePatie Freleng website Pink Panther The Original Pink Panther Shorts DEFAULTSORT Psychedelic Pink Category 1968 films Category American films Category English language films Category Pink ... more details
chembox verifiedrevid 399347229 ImageFile1 AE mescaline.png ImageSize1 180px ImageFile2 AEM 3d sticks.png ImageSize2 200px IUPACName 1 3,4,5 Trimethoxy benzyl propylamine OtherNames Alpha ethyl mescaline br 3,4,5 Trimethoxy alpha ethylphenethylamine br 3,4,5 Trimethoxy 1 ethyl alpha ethyl amine Section1 Chembox Identifiers ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 177522 InChI 1 C13H21NO3 c1 5 10 14 6 9 7 11 15 2 13 17 4 12 8 9 16 3 h7 8,10H,5 6,14H2,1 4H3 SMILES1 O c1cc cc OC c1OC CC N CC C InChIKey DCYONQVUAUEKAJ UHFFFAOYAD StdInChI Ref stdinchicite correct chemspider StdInChI 1S C13H21NO3 c1 5 10 14 6 9 7 11 15 2 13 17 4 12 8 9 16 3 h7 8,10H,5 6,14H2,1 4H3 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey DCYONQVUAUEKAJ UHFFFAOYSA N CASNo 17097 73 3 PubChem 204932 SMILES COc1c cc cc1OC CC N CC OC Section2 Chembox Properties Formula C sub 13 sub H sub 21 sub NO sub 3 sub MolarMass 239.31 g mol Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition AEM , alpha ethylmescaline , or 3,4,5 tri methoxy alpha ethyl group ethyl phenethylamine , is a lesser known Psychedelics, dissociatives and deliriants psychedelic drug . It is an analog chemistry analog of mescaline . AEM was first synthesized by Alexander Shulgin . In his book PiHKAL PiHKAL Phenethylamines i Have Known And Loved , the minimum dosage is listed as 220 mg, and the duration unknown. ref CitePiHKAL ref AEM produces few to no effects. Very little data exists about the pharmacological properties, metabolism, and toxicity of AEM. References reflist See also Mescaline Phenethylamine Psychedelics, dissociatives and deliriants External links http www.erowid.org library books online pihkal pihkal001.shtml AEM Entry in PiHKAL http pihkal.info read.php?domain pk&id 1 AEM Entry in PiHKAL info PiHKAL Category Psychedelic phenethylamines Psychoactive stub fa ... more details
chembox verifiedrevid 413877934 ImageFile1 4 bromo 2,5,beta trimethoxy phenethylamine.png ImageSize1 ImageFile2 BOB 3d sticks.png ImageSize2 IUPACName 2 4 bromo 2,5 dimethoxyphenyl 2 methoxyethanamine OtherNames 4 Bromo 2,5, trimethoxyphenethylamine br 2 4 Bromo 2,5, trimethoxyphenyl ethanamine Section1 Chembox Identifiers InChIKey FYTLQNZPDWLGNU UHFFFAOYAS ChEMBL Ref ebicite correct EBI ChEMBL 191051 StdInChI Ref stdinchicite correct chemspider StdInChI 1S C11H16BrNO3 c1 14 9 5 8 12 10 15 2 4 7 9 11 6 13 16 3 h4 5,11H,6,13H2,1 3H3 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey FYTLQNZPDWLGNU UHFFFAOYSA N CASNo Ref cascite correct ?? CASNo 98537 42 9 ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 21106261 PubChem SMILES COc1cc c cc1Br OC C CN OC InChI 1 C11H16BrNO3 c1 14 9 5 8 12 10 15 2 4 7 9 11 6 13 16 3 h4 5,11H,6,13H2,1 3H3 Section2 Chembox Properties Formula C sub 11 sub H sub 16 sub BrNO sub 3 sub MolarMass 290.15 g mol Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition BOB , or 4 bromo 2,5,beta tri methoxy phenethylamine , is a lesser known Psychedelics, dissociatives and deliriants psychedelic drug . It is the beta Hydroxyl hydroxy analog chemistry analog of 2C B . BOB was first synthesized by Alexander Shulgin . In his book PiHKAL PiHKAL Phenethylamines i Have Known And Loved , the dosage range is listed as 10 20 mg, and the duration listed as 10 20 hours. BOB produces an altered state of consciousness, tinnitus , a pleasant tingling throughout the body, and a sense of awareness. ref CitePiHKAL ref Very little data exists about the pharmacological properties, metabolism, and toxicity of BOB. References reflist See also Phenethylamine Psychedelics, dissociatives and deliriants External links http www.erowid.org library books online pihkal pihkal013.shtml BOB Entry in PiHKAL http pihkal.info read.php?domain pk&id 13 BOB Entry in PiHKAL info PiHKAL Category Psychedeli ... more details
chembox verifiedrevid 401812146 ImageFile1 4 methyl 2,5,beta trimethoxy phenethylamine.svg ImageSize1 ImageFile2 BOD 3d sticks.png ImageSize2 IUPACName 2 2,5 dimethoxy 4 methylphenyl 2 methoxyethanamine OtherNames 4 Methyl 2,5, trimethoxyphenethylamine br 2 4 Methyl 2,5, trimethoxyphenyl ethanamine Section1 Chembox Identifiers InChIKey VTEIFHQUZWABDE UHFFFAOYAC StdInChI Ref stdinchicite correct chemspider StdInChI 1S C12H19NO3 c1 8 5 11 15 3 9 6 10 8 14 2 12 7 13 16 4 h5 6,12H,7,13H2,1 4H3 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey VTEIFHQUZWABDE UHFFFAOYSA N CASNo Ref cascite correct ?? CASNo 98537 41 8 PubChem ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 21106262 SMILES COc1cc C c cc1C CN OC OC InChI 1 C12H19NO3 c1 8 5 11 15 3 9 6 10 8 14 2 12 7 13 16 4 h5 6,12H,7,13H2,1 4H3 Section2 Chembox Properties Formula C sub 12 sub H sub 19 sub NO sub 3 sub MolarMass 225.28 g mol Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition BOD , or 4 methyl 2,5,beta tri methoxy phenethylamine , is a lesser known Psychedelics, dissociatives and deliriants psychedelic drug . It is the beta methoxy analog chemistry analog of 2C D . BOD was first synthesized by Alexander Shulgin . In his book PiHKAL PiHKAL Phenethylamines i Have Known And Loved , the dosage range is listed as 15 25 mg, and the duration listed as 8 16 hours. BOD produces strongly distorted open eye visuals, and some closed eye visuals. It also has an entheogen ic effect and produces humor . ref CitePiHKAL ref Very little data exists about the pharmacological properties, metabolism, and toxicity of BOD. References reflist See also Phenethylamine Psychedelics, dissociatives and deliriants External links http www.erowid.org library books online pihkal pihkal014.shtml BOD Entry in PiHKAL http pihkal.info read.php?domain pk&id 14 BOD Entry in PiHKAL info PiHKAL Category Psychedelic phenethylamines Psychoactive stub fa ... more details
chembox verifiedrevid 397290120 ImageFile1 4 methyl 2,5 dimethoxy beta hydroxyphenethylamine.png ImageSize1 ImageFile2 BOHD 3d sticks.png ImageSize2 IUPACName 2 amino 1 2,5 dimethoxy 4 methylphenyl ethanol OtherNames 4 Methyl 2,5 dimethoxy beta hydroxyphenethylamine br 2 4 Methyl 2,5 dimethoxyphenyl ethan beta hydroxyamine Section1 Chembox Identifiers InChIKey WCURBUJUIMRCCJ UHFFFAOYAU StdInChI Ref stdinchicite correct chemspider StdInChI 1S C11H17NO3 c1 7 4 11 15 3 8 9 13 6 12 5 10 7 14 2 h4 5,9,13H,6,12H2,1 3H3 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey WCURBUJUIMRCCJ UHFFFAOYSA N CASNo Ref changed CASNo 29348 16 1 ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 21106263 PubChem SMILES COc1cc C c cc1C O CN OC InChI 1 C11H17NO3 c1 7 4 11 15 3 8 9 13 6 12 5 10 7 14 2 h4 5,9,13H,6,12H2,1 3H3 Section2 Chembox Properties Formula C sub 11 sub H sub 17 sub NO sub 3 sub MolarMass 211.26 g mol Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition BOHD , or 4 methyl 2,5 di methoxy beta Hydroxyl hydroxy phenethylamine , is a lesser known Psychedelics, dissociatives and deliriants psychedelic drug . It is the beta Hydroxyl hydroxy analog chemistry analog of 2C D . BOHD was first synthesized by Alexander Shulgin . In his book PiHKAL PiHKAL Phenethylamines i Have Known And Loved , the minimum dosage is listed as 50 mg, and the duration unknown. BOHD produces a marked drop in blood pressure . ref CitePiHKAL ref Very little data exists about the pharmacological properties, metabolism, and toxicity of BOHD. References reflist See also Phenethylamine Psychedelics, dissociatives and deliriants External links http www.erowid.org library books online pihkal pihkal016.shtml BOHD Entry in PiHKAL http pihkal.info read.php?domain pk&id 16 BOHD Entry in PiHKAL info PiHKAL Category Psychedelic phenethylamines Psychoactive stub fa ... more details
chembox verifiedrevid 401812293 ImageFile1 3,4,5,beta tetramethoxyphenethylamine.png ImageSize1 ImageFile2 BOM 3d sticks.png ImageSize2 IUPACName 2 methoxy 2 3,4,5 trimethoxyphenyl ethanamine OtherNames 3,4,5,beta Tetramethoxyphenethylamine br 2 3,4,5,beta Tetramethoxyphenyl ethanamine Section1 Chembox Identifiers InChIKey GAKIJEPUVBHWCK UHFFFAOYAE StdInChI Ref stdinchicite correct chemspider StdInChI 1S C12H19NO4 c1 14 9 5 8 11 7 13 16 3 6 10 15 2 12 9 17 4 h5 6,11H,7,13H2,1 4H3 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey GAKIJEPUVBHWCK UHFFFAOYSA N CASNo Ref cascite correct ?? CASNo 98537 40 7 ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 21106265 PubChem SMILES COc1c cc cc1OC C CN OC OC InChI 1 C12H19NO4 c1 14 9 5 8 11 7 13 16 3 6 10 15 2 12 9 17 4 h5 6,11H,7,13H2,1 4H3 Section2 Chembox Properties Formula C sub 12 sub H sub 19 sub NO sub 4 sub MolarMass 241.28 g mol Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition BOM , or 3,4,5,beta tetra methoxy phenethylamine , is a lesser known Psychedelics, dissociatives and deliriants psychedelic drug . It is the beta methoxy analog chemistry analog of Mescaline . BOM was first synthesized by Alexander Shulgin . In his book PiHKAL PiHKAL Phenethylamines i Have Known And Loved , the minimum dosage is listed as 200 mg, and the duration unknown. BOM produces few to no effects. ref CitePiHKAL ref Very little data exists about its pharmacological properties, metabolism, and toxicity. References reflist See also Phenethylamine Psychedelics, dissociatives and deliriants External links http www.erowid.org library books online pihkal pihkal017.shtml BOM Entry in PiHKAL http pihkal.info read.php?domain pk&id 17 BOM Entry in PiHKAL info PiHKAL Category Psychedelic phenethylamines Psychoactive stub fa ... more details
Infobox song See Wikipedia WikiProject Songs Name Psychedelic Woman Type Artist Honny & the Bees Band alt Artist Album A side Recorded Ghana Released Start date 1973 Published Genre Afrobeat Language English Length Duration m 4 s 31 Writer Composer Ernest Honny Label Producer Tracks prev prev no track no next next no Misc Psychedelic Woman is a 1973 Ghanaian song by Honny & the Bees Band. It was written and sung by Ernest Aubrey Honny, ref cite web title Ghana Special Modern Highlife, Afro Sounds & Ghanaian Blues 1968 81 url http www.music releases.com release 1674933 A.B. 20Crentsil Ghana 20Special 20Modern 20Highlife, 20Afro Sounds 20& 20Ghanaian 20Blues 201968 81 work music releases.com accessdate 21 February 2012 ref who worked mainly as a session keyboardist and recording engineer. ref cite news last Duke first John title Talata Heide s Meko url https www.google.com search?tbm bks&tbo 1&q 22Ernest Honny 22 accessdate 22 April 2012 newspaper West Africa date October 31 November 6, 1988 page 2043 ref Over a medium tempo groove, the song begins with a spoken word story concerning a psychedelic woman first spotted at a nightclub. The story ends with a transitional climax to a sung chorus of several voices. There are several more choruses, interspersed with solo singing, then a funky, jazzy electric organ solo, finishing with a brief recap of singing. Part and parcel of the afrobeat sound then exploding out of nearby Nigeria, influences include reggae , James Brown , and perhaps even Britain s Mod subculture mods . ref name Pitchfork ref name Metroactive James Brown cite web last Cahill first Greg title Getting Funky url http www.metroactive.com papers sonoma 06.12.03 brown ... Psychedelic Woman ref Thirty years later it gained a new audience outside of Africa through ... largely ignored in the west, and they range from the pounding and jazzy Psychedelic Woman by Ghana s Honny and the Bees through to... The Guardian ref name Guardian review Psychedelic Woman is irresistible ... more details
and deliriants 2C G Beatrice psychedelic Ganesha , the India n deity External links http www.erowid.org ... info Hallucinogenic phenethylamines PiHKAL DEFAULTSORT Ganesha Psychedelic Category Amphetamines ... more details
Drugbox verifiedrevid 415330726 IUPAC name image F 2.png width 200 Clinical data tradename pregnancy AU A B1 B2 B3 C D X pregnancy US A B C D X pregnancy category legal AU Unscheduled S2 S3 S4 S5 S6 S7 S8 S9 legal CA Schedule I, II, III, IV, V, VI, VII, VIII legal UK GSL P POM CD Class A, B, C legal US OTC Rx only Schedule I, II, III, IV, V legal status routes of administration Pharmacokinetic data bioavailability protein bound metabolism elimination half life excretion Identifiers CAS number ATC prefix ATC suffix DrugBank ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 21106309 ChEMBL Ref ebicite correct EBI ChEMBL 102877 Chemical data chemical formula C 13 H 19 N 1 O 2 molecular weight 221.299 gr mol smiles C1 C2C CC C1CC C N OC CC O2 C InChI 1 C13H19NO2 c1 8 14 4 10 7 13 11 5 9 2 16 13 6 12 10 15 3 h6 9H,4 5,14H2,1 3H3 InChIKey XBHKBTCXRYPZMX UHFFFAOYAL StdInChI Ref stdinchicite correct chemspider StdInChI 1S C13H19NO2 c1 8 14 4 10 7 13 11 5 9 2 16 13 6 12 10 15 3 h6 9H,4 5,14H2,1 3H3 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey XBHKBTCXRYPZMX UHFFFAOYSA N F 2 , or 6 2 amino propyl 5 methoxy 2 methyl 2,3 dihydro benzofuran , is a lesser known Psychedelics, dissociatives and deliriants psychedelic drug . F 2 was first synthesized by Alexander Shulgin . In his book PiHKAL PiHKAL Phenethylamines i Have Known And Loved , the minimum dosage is listed as 15 mg, and the duration unknown. ref name PiHKAL CitePiHKAL ref F 2 produces few to no effects. Very little data exists about the pharmacological properties, metabolism, and toxicity of F 2. References reflist External links http www.erowid.org library books online pihkal pihkal079.shtml F 2 Entry in PiHKAL http pihkal.info read.php?domain pk&id 79 F 2 Entry in PiHKAL info PiHKAL Category Psychedelic phenethylamines Category Benzofurans Category Phenol ethers ... more details
Psychedelic Horseshit is an American band from Columbus, Ohio , that plays a genre of Lo fi music lo fi noise pop that they christened shitgaze . History The group was founded by Matt Whitehurst in 2005 he claims the band s name was coined off the cuff by Sarah Asher when he and a few musician friends landed a slot playing a jam band festival. ref name amg Mark Deming, Allmusic class artist id p988772 pure url yes Psychedelic Horseshit at Allmusic ref The group s lo fi sound, recorded with inexpensive equipment, was solidified over the recording of several CD R releases in 2006 and 2007. ref name amg The group s first 7 arrived in 2007 on Columbus Discount, followed by an EP Siltbreeze picked the band up for a full length, Magic Flowers Droned , in 2007. In 2009 the group re released some of the old CD R material as Golden Oldies , along with new songs as Shitgaze Anthems . ref http pitchfork.com reviews albums 13310 golden oldies shitgaze anthems Review , Pitchfork Media ref They Also released the double seven inch EP Too Many Hits as the final installment of the Columbus Discount Records Year One Singles Club in 2009. They have influenced bands in Brooklyn such as Vivian Girls and Total Slacker according to the New Yorker Magazine in 2010. ref http www.newyorker.com arts events nightlife 2010 01 11 100111goni GOAT nightlife ref Members Matt Whitehurst guitar, keyboards, vocals Rich Johnston percussion Jason Roxas bass Discography Blown Speaker Standards CD R, 2006 King Tubby s Badness Dub CD R, 2006 Who Let the Dogs Out? Columbus Discount Records , 2007 New Wave Hippies EP Half Machine Records 2007 Magic Flowers Droned Siltbreeze , 2007 Golden Oldies LP, 2009 Shitgaze Anthems Woodsist Records , 2009 Magic Flowers Dubbed EP, 2009 Live At Pompeii EP, 2009 Too Many Hits 2x7 Columbus Discount Records , 2009 Acid Tape Fan Death Records , 2010 Laced Fatcat Records, 2011 References Footnotes reflist Further reading http punkmusic.about.com b 2009 03 19 sxsw 2009 psychedelic ... more details
chembox verifiedrevid 399913837 ImageFile1 EEE.png ImageSize1 200px ImageFile2 EEE 3d sticks.png ImageSize2 180px IUPACName 1 Methyl 2 2,4,5 triethoxyphenyl ethylamine OtherNames Section1 Chembox Identifiers InChI 1 C15H25NO3 c1 5 17 13 10 15 19 7 3 14 18 6 2 9 12 13 8 11 4 16 h9 11H,5 8,16H2,1 4H3 InChIKey PVOHHXSVHWUAMS UHFFFAOYAO StdInChI Ref stdinchicite correct chemspider StdInChI 1S C15H25NO3 c1 5 17 13 10 15 19 7 3 14 18 6 2 9 12 13 8 11 4 16 h9 11H,5 8,16H2,1 4H3 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey PVOHHXSVHWUAMS UHFFFAOYSA N CASNo 23693 42 7 ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 21106296 PubChem SMILES CCOc1cc OCC c cc1OCC CC C N Section2 Chembox Properties Formula C sub 15 sub H sub 25 sub NO sub 3 sub MolarMass 267.36 g mol Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition EEE , or 2,4,5 ethoxy triethoxy amphetamine , is a lesser known Psychedelics, dissociatives and deliriants psychedelic drug . It is the ethoxy triethoxy analog chemistry analog of Trimethoxyamphetamine TMA 2 . EEE was first synthesized by Alexander Shulgin . In his book PiHKAL PiHKAL Phenethylamines i Have Known And Loved , both the dosage and duration are unknown. EEE produces few to no effects. Very little data exists about the pharmacological properties, metabolism, and toxicity of EEE. See also Phenethylamine Psychedelics, dissociatives and deliriants External links http www.erowid.org library books online pihkal pihkal073.shtml EEE Entry in PiHKAL http pihkal.info read.php?domain pk&id 73 EEE Entry in PiHKAL info PiHKAL Category Amphetamines Category Phenol ethers Psychoactive stub fa ... more details
chembox verifiedrevid 399913931 ImageFile1 EEM.png ImageSize1 200px ImageFile2 EEM 3d sticks.png ImageSize2 180px IUPACName 2 2,4 Diethoxy 5 methoxy phenyl 1 methyl ethylamine OtherNames Section1 Chembox Identifiers InChI 1 C14H23NO3 c1 5 17 12 9 14 18 6 2 13 16 4 8 11 12 7 10 3 15 h8 10H,5 7,15H2,1 4H3 InChIKey SAFDWWQYGOOGMX UHFFFAOYAW StdInChI Ref stdinchicite correct chemspider StdInChI 1S C14H23NO3 c1 5 17 12 9 14 18 6 2 13 16 4 8 11 12 7 10 3 15 h8 10H,5 7,15H2,1 4H3 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey SAFDWWQYGOOGMX UHFFFAOYSA N CASNo 23693 33 6 ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 21106297 PubChem SMILES CCOc1cc OCC c cc1OC CC C N Section2 Chembox Properties Formula C sub 14 sub H sub 23 sub NO sub 3 sub MolarMass 253.34 g mol Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition EEM , or 2,4 di ethoxy 5 methoxy amphetamine , is a lesser known Psychedelics, dissociatives and deliriants psychedelic drug . It is a diethoxy methoxy analog chemistry analog of Trimethoxyamphetamine TMA 2 . EEM was first synthesized by Alexander Shulgin . In his book PiHKAL PiHKAL Phenethylamines i Have Known And Loved , both the dosage and duration are unknown. EEM produces few to no effects. Very little data exists about the pharmacological properties, metabolism, and toxicity of EEM. See also Phenethylamine Psychedelics, dissociatives and deliriants External links http www.erowid.org library books online pihkal pihkal074.shtml EEM Entry in PiHKAL http pihkal.info read.php?domain pk&id 74 EEM Entry in PiHKAL info PiHKAL Category Amphetamines Category Phenol ethers Psychoactive stub fa ... more details
chembox verifiedrevid 399914040 ImageFile 2,5 diethoxy 4 methoxyamphetamine.png ImageSize 200px IUPACName 2 2,5 Diethoxy 4 methoxyphenyl 1 methylethylamine OtherNames Section1 Chembox Identifiers InChI 1 C14H23NO3 c1 5 17 12 9 13 16 4 14 18 6 2 8 11 12 7 10 3 15 h8 10H,5 7,15H2,1 4H3 InChIKey IVHFHHXLFFHTTA UHFFFAOYAT SMILES1 COc1cc OCC c cc1OCC CC C N StdInChI Ref stdinchicite correct chemspider StdInChI 1S C14H23NO3 c1 5 17 12 9 13 16 4 14 18 6 2 8 11 12 7 10 3 15 h8 10H,5 7,15H2,1 4H3 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey IVHFHHXLFFHTTA UHFFFAOYSA N CASNo 23693 34 7 ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 21106298 PubChem SMILES C1 CC C C C1CC C N OCC OC OCC Section2 Chembox Properties Formula C sub 14 sub H sub 23 sub NO sub 3 sub MolarMass 253.341 g mol Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition EME , or 2,5 di ethoxy 4 methoxy amphetamine , is a lesser known Psychedelics, dissociatives and deliriants psychedelic drug . It is a diethoxy methoxy analog chemistry analog of Trimethoxyamphetamine TMA 2 . EME was first synthesized by Alexander Shulgin . In his book PiHKAL PiHKAL Phenethylamines i Have Known And Loved , both the dosage and duration are unknown. EME produces few to no effects. Very little data exists about the pharmacological properties, metabolism, and toxicity of EME. See also Phenethylamine Psychedelics, dissociatives and deliriants External links http www.erowid.org library books online pihkal pihkal075.shtml EME Entry in PiHKAL http pihkal.info read.php?domain pk&id 75 EME Entry in PiHKAL info PiHKAL Category Amphetamines Category Phenol ethers Psychoactive stub fa ... more details
chembox verifiedrevid 399914160 ImageFile1 EMM.png ImageSize1 200px IUPACName 2 2 Ethoxy 4,5 dimethoxyphenyl 1 methylethylamine OtherNames Section1 Chembox Identifiers InChI 1 C13H21NO3 c1 5 17 11 8 13 16 4 12 15 3 7 10 11 6 9 2 14 h7 9H,5 6,14H2,1 4H3 InChIKey SKRNTJDDBVAEGB UHFFFAOYAE SMILES1 COc1cc OCC c cc1OC CC C N StdInChI Ref stdinchicite correct chemspider StdInChI 1S C13H21NO3 c1 5 17 11 8 13 16 4 12 15 3 7 10 11 6 9 2 14 h7 9H,5 6,14H2,1 4H3 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey SKRNTJDDBVAEGB UHFFFAOYSA N CASNo 23693 30 3 ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 21106299 PubChem SMILES C1 CC C C C1CC C N OC OC OCC Section2 Chembox Properties Formula C sub 13 sub H sub 21 sub NO sub 3 sub MolarMass 239.314 g mol Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition EMM , or 2 ethoxy 4,5 di methoxy amphetamine , is a lesser known Psychedelics, dissociatives and deliriants psychedelic drug . It is a dimethoxy ethoxy analog chemistry analog of Trimethoxyamphetamine TMA 2 . EMM was first synthesized by Alexander Shulgin . In his book PiHKAL PiHKAL Phenethylamines i Have Known And Loved , both the dosage and duration are unknown. EMM produces few to no effects. Very little data exists about the pharmacological properties, metabolism, and toxicity of EMM. See also Phenethylamine Psychedelics, dissociatives and deliriants External links http www.erowid.org library books online pihkal pihkal076.shtml EMM Entry in PiHKAL http pihkal.info read.php?domain pk&id 76 EMM Entry in PiHKAL info PiHKAL Category Amphetamines Category Phenol ethers Psychoactive stub fa ... more details
chembox verifiedrevid 400292910 ImageFile MEE.png ImageSize 200px IUPACName 2 4,5 Diethoxy 2 methoxy phenyl 1 methyl ethylamine OtherNames 2 Methoxy 4,5 diethoxyphenethylamine Section1 Chembox Identifiers InChI 1 C14H23NO3 c1 5 17 13 8 11 7 10 3 15 12 16 4 9 14 13 18 6 2 h8 10H,5 7,15H2,1 4H3 InChIKey LKJRFMXILZHUHU UHFFFAOYAA StdInChI Ref stdinchicite correct chemspider StdInChI 1S C14H23NO3 c1 5 17 13 8 11 7 10 3 15 12 16 4 9 14 13 18 6 2 h8 10H,5 7,15H2,1 4H3 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey LKJRFMXILZHUHU UHFFFAOYSA N CASNo 23693 35 8 ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 21106337 PubChem SMILES CCOc1cc OC c cc1OCC CC C N Section2 Chembox Properties Formula C sub 14 sub H sub 23 sub NO sub 3 sub MolarMass 253.34 Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition MEE , or 2 methoxy 4,5 di ethoxy amphetamine , is a lesser known Psychedelics, dissociatives and deliriants psychedelic drug . It is a diethoxy methoxy analog chemistry analog of Trimethoxyamphetamine TMA 2 . MEE was first synthesized by Alexander Shulgin . In his book PiHKAL PiHKAL Phenethylamines i Have Known And Loved , both the dosage and duration are unknown. MEE produces few to no effects. Very little data exists about the pharmacological properties, metabolism, and toxicity of MEE. See also Phenethylamine Psychedelics, dissociatives and deliriants External links http www.erowid.org library books online pihkal pihkal121.shtml MEE entry in PiHKAL http pihkal.info read.php?domain pk&id 121 MEE entry in PiHKAL info PiHKAL Category Amphetamines Psychoactive stub fa ... more details
Here is a table of data skip past it to edit the text. border 1 cellpadding 2 cellspacing 0 align right style margin left 1em colspan 2 bgcolor cccccc TOM IUPAC nomenclature Chemical name Thio Thio mescaline Chemical formula C sub 12 sub H sub 19 sub NOS colspan 2 align center Image 2 TOM.png 175px 2 TOM, an example of a TOM compound TOM , or methyl Thio thio methyl methoxy amphetamine , is a series of lesser known Psychedelics, dissociatives and deliriants psychedelic drugs and substituted amphetamines . 2 TOM and 5 TOM are the 2 and 5 methylthio analogs of DOM DOM STP , respectively. They were first synthesized by Alexander Shulgin and written up in his book PiHKAL PiHKAL Phenethylamines i Have Known And Loved . Very little data is known about their dangers or toxicity. TOM compounds Image 2 TOM.png thumb right 140px 2 TOM, or 5 methoxy 4 methyl 2 methylthio amphetamine Image 5 TOM.png thumb right 140px 5 TOM, or 2 methoxy 4 methyl 5 methylthio amphetamine 2 TOM Dosage 60 100 mg Duration 8 10 hours Effects strong closed eye visuals upon listening to music, on the Shulgin Rating Scale 5 TOM Dosage 30 50 mg Duration 6 10 hours Effects open and closed eye visuals, psychedelia , hallucinations See also Phenethylamine Psychedelics, dissociatives and deliriants PiHKAL DOM External links http www.erowid.org library books online pihkal pihkal171.shtml 2 TOM entry in PiHKAL http pihkal.info read.php?domain pk&id 171 2 TOM entry in PiHKAL info http www.erowid.org library books online pihkal pihkal172.shtml 5 TOM entry in PiHKAL http pihkal.info read.php?domain pk&id 172 5 TOM entry in PiHKAL info PiHKAL Category Amphetamines ... more details
Here is a table of data skip past it to edit the text. border 1 cellpadding 2 cellspacing 0 align right style margin left 1em colspan 2 bgcolor cccccc TOET IUPAC nomenclature Chemical name Thio Thio mescaline Chemical formula C sub 13 sub H sub 21 sub NOS colspan 2 align center Image 2 TOET.png 175px 2 TOET, an example of a TOET compound TOET , or methyl Thio thio ethyl group ethyl methoxy amphetamine , is a series of lesser known Psychedelics, dissociatives and deliriants psychedelic drugs and substituted amphetamines . 2 TOET and 5 TOET are the 2 and 5 methylthio analogs of DOET , respectively. They were first synthesized by Alexander Shulgin and written up in his book PiHKAL PiHKAL Phenethylamines i Have Known And Loved . Very little data is known about their dangers or toxicity. TOET compounds Image 2 TOET.png thumb right 140px 2 TOET, or 2 methylthio 4 ethyl 5 methoxyphenethylamine Image 5 TOET.png thumb right 140px 5 TOET, or 5 methylthio 4 ethyl 2 methoxy phenethylamine 2 TOET Dosage 65 mg or greater Duration unknown Effects few to none 5 TOET Dosage 12 25 mg Duration 8 24 hours Effects pathologic nystagmus nystagmus , strong LSD like visuals and hallucinations , eyes closed imagery See also Phenethylamine Psychedelics, dissociatives and deliriants PiHKAL DOET External links http www.erowid.org library books online pihkal pihkal169.shtml 2 TOET entry in PiHKAL http pihkal.info read.php?domain pk&id 169 2 TOET in PiHKAL info http www.erowid.org library books online pihkal pihkal170.shtml 5 TOET entry in PiHKAL http pihkal.info read.php?domain pk&id 170 5 TOET in PiHKAL info PiHKAL Category Amphetamines ... more details
chembox verifiedrevid 400293175 Name 2,5 dimethoxy 4 propoxyamphetamine ImageFile MPM.png ImageSize IUPACName 1 2,4 dimethoxy 5 propoxyphenyl propan 2 amine OtherNames Section1 Chembox Identifiers ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 21106339 InChI 1 C14H23NO3 c1 5 6 18 14 8 11 7 10 2 15 12 16 3 9 13 14 17 4 h8 10H,5 7,15H2,1 4H3 InChIKey FTJOFRCENIVFLC UHFFFAOYAE StdInChI Ref stdinchicite correct chemspider StdInChI 1S C14H23NO3 c1 5 6 18 14 8 11 7 10 2 15 12 16 3 9 13 14 17 4 h8 10H,5 7,15H2,1 4H3 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey FTJOFRCENIVFLC UHFFFAOYSA N CASNo PubChem SMILES COc1cc OC c cc1OCCC CC C N Section2 Chembox Properties Formula C sub 14 sub H sub 23 sub NO sub 3 sub MolarMass 253.337 g mol Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition MPM 2,5 di methoxy 4 Propane prop oxy amphetamine is a lesser known Psychedelics, dissociatives and deliriants psychedelic drug and a substituted amphetamine . MPM was first synthesized by Alexander Shulgin . In his book PiHKAL PiHKAL Phenethylamines i Have Known And Loved , dosage is given as 30 mg or more and duration probably short . MPM is of low potency and produced only slight effects at the highest dose reported in PiHKAL of 30 mg, although its effects at higher doses than this have not been reported. Very little data exists about the pharmacological properties, metabolism, and toxicity of MPM. See also Phenethylamine s Psychedelics, dissociatives and deliriants External links http www.erowid.org library books online pihkal pihkal1138.shtml MPM entry in PiHKAL on Erowid http pihkal.info read.php?domain pk&id 138 MPM entry in PiHKAL info PiHKAL Category Amphetamines Category Phenol ethers Psychoactive stub fa ... more details
chembox verifiedrevid 400293093 ImageFile MME.png ImageSize 200px IUPACName 1 5 ethoxy 2,4 dimethoxyphenyl propan 2 amine OtherNames Section1 Chembox Identifiers InChI 1 C13H21NO3 c1 5 17 13 7 10 6 9 2 14 11 15 3 8 12 13 16 4 h7 9H,5 6,14H2,1 4H3 InChIKey NAMNXRTWJMASNT UHFFFAOYAR StdInChI Ref stdinchicite correct chemspider StdInChI 1S C13H21NO3 c1 5 17 13 7 10 6 9 2 14 11 15 3 8 12 13 16 4 h7 9H,5 6,14H2,1 4H3 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey NAMNXRTWJMASNT UHFFFAOYSA N CASNo 23693 32 5 ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 21106338 PubChem SMILES COc1cc OC c cc1OCC CC C N Section2 Chembox Properties Formula C sub 13 sub H sub 21 sub NO sub 3 sub MolarMass 239.311 g mol Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition MME , or 2,4 di methoxy 5 ethoxy amphetamine , is a lesser known Psychedelics, dissociatives and deliriants psychedelic drug . It is a dimethoxy ethoxy analog chemistry analog of Trimethoxyamphetamine TMA 2 . MME was first synthesized by Alexander Shulgin . In his book PiHKAL PiHKAL Phenethylamines i Have Known And Loved , the minimum dosage is listed as 40 mg, and the duration listed as 6 10 hours. Shulgin gives MME a on the Shulgin Rating Scale . Very little data exists about the pharmacological properties, metabolism, and toxicity of MME. See also Phenethylamine Psychedelics, dissociatives and deliriants External links http www.erowid.org library books online pihkal pihkal136.shtml MEM entry in PiHKAL http pihkal.info read.php?domain pk&id 136 MEM entry in PiHKAL info PiHKAL Category Amphetamines Category Phenol ethers Psychoactive stub fa ... more details
chembox verifiedrevid 399530822 ImageFile1 Ariadne.svg IUPACName 1 2,5 Dimethoxy 4 methyl benzyl propylamine OtherNames 4 Methyl 2,5 dimethoxy alpha ethylphenethylamine br 4 Methyl 2,5 dimethoxybutanamine Section1 Chembox Identifiers ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 148565 InChI 1 C13H21NO2 c1 5 11 14 7 10 8 12 15 3 9 2 6 13 10 16 4 h6,8,11H,5,7,14H2,1 4H3 t11 m1 s1 InChIKey MLYCFWZIAJAIGW LLVKDONJBY InChI1 1 C13H21NO2 c1 5 11 14 7 10 8 12 15 3 9 2 6 13 10 16 4 h6,8,11H,5,7,14H2,1 4H3 InChIKey1 MLYCFWZIAJAIGW UHFFFAOYAX SMILES1 O c1cc c OC cc1CC N CC C C StdInChI Ref stdinchicite correct chemspider StdInChI 1S C13H21NO2 c1 5 11 14 7 10 8 12 15 3 9 2 6 13 10 16 4 h6,8,11H,5,7,14H2,1 4H3 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey MLYCFWZIAJAIGW UHFFFAOYSA N CASNo 52842 59 8 PubChem 169886 SMILES O c1cc c OC cc1C C H N CC C C Section2 Chembox Properties Formula C sub 13 sub H sub 21 sub NO sub 2 sub MolarMass 223.31 g mol ExactMass 223.157229 Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition Ariadne Dimoxamine , Et DOM , or 4 methyl 2,5 di methoxy alpha ethyl group ethyl phenethylamine , is a lesser known Psychedelics, dissociatives and deliriants psychedelic drug . It is a homologue chemistry homologue of 2C D and 2,5 Dimethoxy 4 methylamphetamine DOM . Ariadne was first synthesized by Alexander Shulgin . In his book PiHKAL PiHKAL Phenethylamines i Have Known And Loved , Shulgin reported testing Ariadne up to a dose of 32 mg, and reported that it produces psychedelia and a bare threshold. ref CitePiHKAL ref Very little data exists about the pharmacological properties, metabolism, and toxicity of Ariadne in humans apart from Shulgin s limited testing. However, in more recent animal studies, Et DOM was shown to produce stimulus generalisation in rats trained to respond to the drug MDMA . ref Glennon RA. MDMA Like Stimulus Effects of Ethyltryptamine and th ... more details
chembox verifiedrevid 399319677 ImageFile1 4 D.svg ImageSize1 200px ImageFile2 4 D 3d sticks.png ImageSize2 200px IUPACName 3,5 Methoxy 4 trideuteromethoxyphenethylamine OtherNames Section1 Chembox Identifiers ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 21106241 InChI 1 C12H19NO3 c1 8 13 5 9 6 10 14 2 12 16 4 11 7 9 15 3 h6 8H,5,13H2,1 4H3 i4D3 SMILES1 2H C 2H 2H Oc1c cc cc1OC CC C N OC InChIKey WGTASENVNYJZBK GKOSEXJEEY StdInChI Ref stdinchicite correct chemspider StdInChI 1S C12H19NO3 c1 8 13 5 9 6 10 14 2 12 16 4 11 7 9 15 3 h6 8H,5,13H2,1 4H3 i4D3 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey WGTASENVNYJZBK GKOSEXJESA N CASNo PubChem SMILES 2H C 2H 2H Oc1c OC cc cc1OC CC N C Section2 Chembox Properties Formula C sub 11 sub H sub 14 sub NO sub 3 sub D sub 3 sub MolarMass 228.28 g mol Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition 4 D , or 3,5 methoxy 4 tri Deuterium deutero methoxy phenethylamine , is a lesser known Psychedelics, dissociatives and deliriants psychedelic drug . It is one of the only phenethylamine s that contain deuterium , the other being beta D . It is also the 4 trideuteromethoxy analogue of 2C H . It may be prepared either as a sulfate salt chemistry salt or a hydrochloride salt. 4 D was first synthesized by Alexander Shulgin . In his book PiHKAL PiHKAL Phenethylamines i Have Known And Loved , the dosage is listed as approximately 200 400 mg for the sulfate salt, and 178 356 mg for the hydrochloride salt. 4 D lasts for approximately 12 hours. It causes closed eye visuals, mild open eye visuals, color distortion, and mydriasis . ref CitePiHKAL ref Very little data exists about the pharmacological properties, metabolism, and toxicity of 4 D. See also Phenethylamine Psychedelics, dissociatives and deliriants References reflist External links http www.erowid.org library books online pihkal pihkal050.shtml 4 D Entry in PiHKAL http pihkal.info re ... more details
chembox verifiedrevid 413307056 ImageFile1 2,5 dimethoxy 4 methylthioamphetamine.svg ImageSize1 200px IUPACName 2 2,5 Dimethoxy 4 methylsulfanyl phenyl 1 methylethylamine OtherNames 2,5 Dimethoxy 4 methylthioamphetamine br 1 4 Methylthio 2,5 dimethoxyphenyl 2 aminopropane Section1 Chembox Identifiers ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 126887 InChI 1 C12H19NO2S c1 8 13 5 9 6 11 15 3 12 16 4 7 10 9 14 2 h6 8H,5,13H2,1 4H3 InChIKey COBYBOVXXDQRAU UHFFFAOYAK SMILES1 O c1cc c OC cc1SC CC N C C ChEMBL Ref ebicite correct EBI ChEMBL 447830 StdInChI Ref stdinchicite correct chemspider StdInChI 1S C12H19NO2S c1 8 13 5 9 6 11 15 3 12 16 4 7 10 9 14 2 h6 8H,5,13H2,1 4H3 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey COBYBOVXXDQRAU UHFFFAOYSA N CASNo 61638 07 1 PubChem 143828 SMILES C1 C C C C C1 SC OC CC C N OC Section2 Chembox Properties Formula C sub 12 sub H sub 19 sub NO sub 2 sub S MolarMass 240.35 g mol Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition Aleph , or 2,5 di methoxy 4 methyl Thio thio amphetamine , is a psychedelic Psychedelics, dissociatives and deliriants hallucinogenic drug and a substituted amphetamine of the phenethylamine class of compounds, which can be used as an entheogen . It was first synthesized by Alexander Shulgin . In his book PiHKAL PiHKAL Phenethylamines i Have Known And Loved , Shulgin lists the dosage range as 5 10 mg. ref CitePiHKAL ref According to Shulgin, the effects of aleph typically last for 6 to 8 hours. Homologues Aleph 2 Image 2,5 dimethoxy 4 ethylthioamphetamine.svg thumb left 200px Aleph 2 br style clear left Dosage 4 8 mgs Duration 8 16 hours Effects Strong visuals 2C psychedelics 2C analog 2C T 2 CAS number 185562 00 9 SMILES C1 C C C C C1 SCC OC CC C N OC Aleph 4 Image Aleph 4.svg thumb left 200px Aleph 4 br style clear left Dosage 7 12 mgs Duration 12 20 hours Effects profound and deep learning experiences Alexander Shulg ... more details
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