Amphetamine Syntheses Overview & Reference Guide for Professionals (Psychoactive Synthesis Series Vol 1)
by: Otto Snow

Amphetamine Syntheses Overview & Reference Guide for Professionals
By Otto Snow

Product Description:

the most comprehensive reference guide on the syntheses of amphetamines, phenyethylamines, ephedrine, cathinone, their immediate precursors and precursors. This includes the syntheses of mescaline and all popular psychedelic amphetamines including MDMA, MDEA, 2CB, TMA, DOB, DOM etc.

Hundreds of reactions are described including a review of the Controlled Substance Analogue Act. Many of the reactions include: Reductions of phenyl-2-propanone using aluminum amalgam, aluminum turnings or aluminum foil. The preparation of aluminum amalgam, mercury bichloride. Electrolytic reductions. Phenyl-2-nitropropenes From pseudonitrosites. Phenyl-2-propanone (P-2-P) from phenylacetic acid; from phenyl-2-nitropropenes; from monochloroacetone; from phenyl-1,2-propanediol. (Friedel-Crafts Reaction); ketones from phenols. The preparation of amphetamines (Leuckart-Wallach Reaction); (Ritter Reaction); (Willgerodt Reaction); (Hofmann Reaction). Amphetamines From phenyl-2-bromopropane. Preparation of cathinone. The preparation of substituted benzaldehydes; (Duff Reaction); (Elbs Persulfate Reaction); Phenols From Benzaldehydes; (Dakin Reaction). Benzaldehydes from Propenylbenzenes. Ally and propenylbenzenes from natural sources. Propenylbenzenes From phenyl-1-propanols. Phenylpropenes by thermal dehydration. Propenylbenzenes from benzenes; (Quelet Reaction). Preparation of phenyl-1-propanols using the Grignard Reagent; by the reduction of propiophenone. Preparation of cinnamic acids. Cinnamic acids from coumarins. Naturally occurring coumarins. The Crossed Aldol Condensation. The Haloform Reaction. Hydrocinnamic acid from propiophenone. Preparation of nitroethane. Preparation of 4-bromoamphetamine and 4-chloroamphetamine. Preparation of neurotransmitters & neurotoxins and much more…

80 references from scientific and medical journals.

Indexed for fast identification of chemicals, reactions and products.

AMAZON DESCRIPTION

Amphetamine Syntheses Overview & Reference Guide for Professionals (Paperback)
by Otto Snow

Product Details
Paperback: 257 pages
Publisher: Thoth Press (June 2, 1998)
Language: English
ISBN-10: 0966312805
ISBN-13: 978-0966312805

Editorial Reviews Review
Snow’s new book Amphetamine Syntheses is an excellent volley filled with facts, testimony, history and of course lots of chemistry. I found the book quite readable, easy to understand, and noteworthy so far as presenting the overlooked position of the independent neuroscientist and his world. I suspect you will see this book being used by a lot of lawyers, forensic chemists, social scientists and drug philosophers looking for some truth, facts, sanity and common-sense – all collected in one spot. — Psychedelics ReImagined, Thomas Lyttle; Autonomedia 1998

Product Description
the most comprehensive reference guide on the syntheses of amphetamines, phenyethylamines, ephedrine, cathinone, their immediate precursors and precursors. This includes the syntheses of mescaline and all popular psychedelic amphetamines including MDMA, MDEA, 2CB, TMA, DOB, DOM etc. Hundreds of reactions are described including a review of the Controlled Substance Analogue Act. Many of the reactions include: Reductions of phenyl-2-propanone using aluminum amalgam, aluminum turnings or aluminum foil. The preparation of aluminum amalgam, mercury bichloride. Electrolytic reductions. Phenyl-2-nitropropenes From pseudonitrosites. Phenyl-2-propanone (P-2-P) from phenylacetic acid; from phenyl-2-nitropropenes; from monochloroacetone; from phenyl-1,2-propanediol. (Friedel-Crafts Reaction); ketones from phenols. The preparation of amphetamines (Leuckart-Wallach Reaction); (Ritter Reaction); (Willgerodt Reaction); (Hofmann Reaction). Amphetamines From phenyl-2-bromopropane. Preparation of cathinone. The preparation of substituted benzaldehydes; (Duff Reaction); (Elbs Persulfate Reaction); Phenols From Benzaldehydes; (Dakin Reaction). Benzaldehydes from Propenylbenzenes. Ally and propenylbenzenes from natural sources. Propenylbenzenes From phenyl-1-propanols. Phenylpropenes by thermal dehydration. Propenylbenzenes from benzenes; (Quelet Reaction). Preparation of phenyl-1-propanols using the Grignard Reagent; by the reduction of propiophenone. Preparation of cinnamic acids. Cinnamic acids from coumarins. Naturally occurring coumarins. The Crossed Aldol Condensation. The Haloform Reaction. Hydrocinnamic acid from propiophenone. Preparation of nitroethane. Preparation of 4-bromoamphetamine and 4-chloroamphetamine. Preparation of neurotransmitters & neurotoxins and much more… 380 references from scientific and medical journals. Indexed for fast identification of chemicals, reactions and products.

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THC & Tropacocaine
by: Otto Snow

THC & Tropacocaine
By Otto Snow

Product Description:

THC is a new miracle medication, used to treat sleep disorders allergies, inflammatory diseases, auto immune disorders, migraines, addictions, post traumatic stress disorder, anorexia, etc.

Syntheses of THC and chemical analogs are described. Human testing are also included. The extraction of THC (eg. 40%, 70% and 92% THC Hash Oil) from cannabis is detailed. Isomerisation: a quick route from cannabidiol.

The discovery of its endogenous ligand, anandamide (a fatty acid amide) has revolutionized the investigation of this new neurotransmitter system. Anandamides have been used in the treatment of insomnia, allergies and post traumatic stress disorder yet remain undeveloped. Anandamides will replaced THC and marijuana because of ease of synthesis; preparation from commonly available grocery store oils (eg. olive oil). Multiple reactions are explained.

Tropacocaine was discovered as a trace alkaloid in Coca leaves from Java. It is longer acting and less toxic than cocaine.

Tropacocaine is prepared from atropine obtained from nightshade plants. The synthesis of tropacocaine from Datura (eg. nightshade) is described and referenced. Reactions have been translated into English. Millions of Americans are addicted to cocaine and crack, yet tropacocaine has never been studied to assess its value as a replacement medication. 400 refs. Color cover. Laminated.

AMAZON INFO

THC & Tropacocaine (Paperback)
by Otto Snow(Author)

Product Details
Paperback: 182 pages
Publisher: THOTH (August 31, 2004)
Language: English
ISBN-10: 0966312856
ISBN-13: 978-0966312850

Editorial Reviews
Product Description
THC is a new miracle medication, used to treat sleep disorders allergies, inflammatory diseases, auto immune disorders, migraines, addictions, post traumatic stress disorder, anorexia, etc.
Syntheses of THC and chemical analogs are described. Human testing are also included. The extraction of THC (eg. 40%, 70% and 92% THC Hash Oil) from cannabis is detailed. Isomerisation: a quick route from cannabidiol.

The discovery of its endogenous ligand, anandamide (a fatty acid amide) has revolutionized the investigation of this new neurotransmitter system. Anandamides have been used in the treatment of insomnia, allergies and post traumatic stress disorder yet remain undeveloped. Anandamides will replaced THC and marijuana because of ease of synthesis; preparation from commonly available grocery store oils (eg. olive oil). Multiple reactions are explained.

Tropacocaine was discovered as a trace alkaloid in Coca leaves from Java. It is longer acting and less toxic than cocaine.

Tropacocaine is prepared from atropine obtained from nightshade plants. The synthesis of tropacocaine from Datura (eg. nightshade) is described and referenced. Reactions have been translated into English. Millions of Americans are addicted to cocaine and crack, yet tropacocaine has never been studied to assess its value as a replacement medication. 400 refs. Color cover. Laminated.

From the Publisher
Book Includes:

Medical Cannabis: CANNABIS. U.S. (Br.) CANNABIS Cannab; THC; Synhexyl Stereochemical Requirements for Cannabimimetic Activity Cannabinoid Receptors CB2 Agonist Treament of Autoimmunine Disorders CB-2 Receptor Agonist Compounds Inhibition of Cell Proliforation; Cannabinoids in the Treatment of Glaucoma Anandamide Amidase Inhibitors as Analgesic Agents CB1 Agonists for Use in Brain Trauma Erratic Gastrointestial Absorbtion of delta-9-Tetrahydrocannabinol Treating Mental Diseases, Inflammation and Pain with Anandamides

Extraction of Delta-9-Tetrahydrocannabinol from Cannabis Extraction of Cannabis Buds (41% THC Oil) Extraction of Cannabis Buds 2 (40% THC Oil) (92% THC Oil) Preparing Delta-9-Tetrahydrocannabinol Reprocessing of the Residue Left After Fractional Distillation of Cannabis Extracts (82% THC Yellow Oil); THC Syntheses Water Soluble Derivatives of Cannabinoids Synthesis of Compound (4) Ketones from Nitriles THC in the Treatment of Glaucoma in Patients who can not take Beta-blockers Compositions useful as a cannabinoid receptor probe Production of 6,12-Dihydro-6-hydroxy-cannabidiol Production of trans-delta-9-Tetrahydrocannabinol Production of 6,12-Dihydro-6-hydroxy-cannabidiol Production of trans-delta-9-Detrahydrocannabinol Preparation of cis-p-Menth-2-ene-1,8,-diol Novel Tetrahydrocannabinol Type Compounds Preparation of (-)-6a,10a-trans-6a,7,8,10a-Tetrahydrodibenzo[b,d]-pyrans Preparation of Optically Active trans-Hexahydrodibenzopyranones 1-Hydroxy-3-(1,1-dimethylheptyl)-6,6-dimethyl-6,6aR,7,8,10,10aR-hexahydro-9-H-dibenzo[b,d]pyran-9-one Producing 6a,10a-trans-6a,7,8,10a-Tetrahydrodibenzo (b,d)-pyrans 3-(1,2-Dimethylheptyl)-6a,7,10,10a-tetra-hydro-1-hydroxy-6,6,9-trimethyl-6H-dibenzo [b,d]pyran

5-Alkylresorcinols: Preparation of l-Hydroxy-2,6-dimethoxy-4-(tertiaryalkyl)benzene 1-Hydroxy-2,6-dimethoxy-4-(1,1-dimethylheptyl)benzene Divarin Dimethyl Ether from 3,4,5-Trimethoxy-propiophenone Reduction of Ketones to Resorcinols Synthesis of 5-Alkylresorcinols; Synthesis of 5-Ethylresorcinol Preparation of Hexylresorcinol by Electrolytic Reduction of Hexanoylresorcinol Synthesis of 5-Methylresorcinol (Orcinol) 5-Alkylresorcinol from Demethylation of 1-(Alkyl)-3,5-Dimethoxybenzene Demethylation Using Pyridine 5-(1,1-dimethylheptyl)resorcinol Demethylation Using 48% Hydrobromic Acid 5-(1,1-Dimethylheptyl)resorcinol ; Preparation of 5-Alkoxyresorcinols Preparation of Phloroglucinol and its Mono-ethers Preparation of Compounds with Marijuana Activity Formation of Tetrahydrocannabinols by Isomerization of Cannabidiol A. By p-toluenesulfonic acid; B. By sulfuric acid; C. By pyridine hydrochloride; D. By phosphoric acid; E. Sulfamic acid; zinc chloride

Converting cis-Hexahydrodibenzo[b,d]pyran-9-ones to trans-Hexahydrodibenzo[b,d]-pyran-9-ones dl-trans-1-Hydroxy-3-(1,1-dimethyl-heptyl) -6,6-dimethyl-6,6a,7,8,10,10a-hexahydro-9H- dibenzo[b,d]pyran-9-one dl-trans-1-Hydroxy-3-n-pentyl-6,6-dimethyl-6,6a,7,8,10,10a-hexahydro-9H-dibenzo[b,d]pyran-9-one dl-trans-1-Hydroxy-3-(1,1-dimethyl-heptyl)-6,6-dimethyl-6,6a,7,8,10,10a-hexahydro-9H-dibenzo[b,d]pyran-9-one Stereoselective Preparation of Hexahydrodibenzopyranones and intermediates (-)-trans-1-Hydroxy-3-(1,1-dimethyl-heptyl)-6,6-dimethyl-6,6a,7,8,10,10a-hexahydro-9H-dibenzo[b,d]pyran-9-one; Acetylation of THC

Delta 1-THC-7-oic acid Analgesic and Anti-inflammatory Agents Platelet Activating Factor Antagonist Non-psychoactive Derivatives of 鈭?-THC-7-oic Acid which have Analgesic and Anti-inflammatory Properties Synthesis of (3R,4R)-鈭?-THC-DMH-7-oic Acid Acetate

Andanamides: Fatty Acid Amides; Preparation of Arachidonyl Ethanolamide Compounds Isolated from the Brain and Synthesized Synthetic Compounds Prepared and Tested Anandamide Amidase Inhibitors as Analgesic Agents Treating Anxiety and Mood Disorders with Oleamide

Fatty Acid Amides Preparation from Common Household Oils Preparation of Oleamide The Reactions Used N-Substituted Amides of Natural Fatty Acids Preparation of N-Methyl Linseed Oil Fatty Acid Amide Preparation of N-Cyclohexyl Linseed Oil Fatty Acid Amide Preparation of Lauric Diethanolamide from Lauroyl Chloride Preparation of Cocoa Fatty Acid Amide Using the Aminolysis Method

Industrial Manufacture of Fatty Acid Ethanolamides reparation of Oleic Acid Monoethanolamide Purification of Fatty Acid Amides Using Urea Preparation of Olive Oil and Coconut Oil Ethanolamides Preparation of Fatty Acids; Isolation of Linoleic Acid Isolation of Oleic Acid from Olive Oil; Production of Monoalkyolamines

TROPACOCAINE

Coca, The Source of Cocaine; COCAINA. U.S., Br.; COCAINE HYDROCHLORIDUM. U.S., Br. Atropine and the Tropeines Cocaine and the Local Anesthetic; Tropacocaine Benzoyl Ester of Ecgonine Using Benzoic Anhydride Tropacocaine from Pseudo-tropine & Benzoic Anhydride Pseudotropine by Electrolytic Reduction of Tropine Tropineone by Oxidation of Tropine; Extraction of Pseudotropine Pseudotropine by the Electrolytic Reduction of Tropinone Tropinone by the Oxydation of Tropine; Tropinone by the Oxydation of Pseudotropine Tropinone by the Electrolytic Reduction of Tropine or Pseudotropine Benzoic Anhydride

Narcotic Daturas Origin of the Name Jimson, or Jamestown Weed; The Huaca-Cachu of Peru Datura Alkaloids ; Hyoscyamine and Atropine; Atropine Sulphate Hyoscine or Scopolamine ; Extraction of Atropine Growing Datura and Related Species BELLADONNA Atropa belladonna; Atropa belladonna (Belladonna) Cultivation Datura stramonium L. (Jimson Weed) ; Datura stramonium (Jimson weed) Cultivation Hyoscyamus niger (Henbane) Cultivation ; Solanum nigram L. (Black Nightshade)

Anyone interested in the construction and future of CB-1 agonists (eg. THC, Oleamide) or cocaine agonists (eg. tropacocaine) will find this book cutting edge.

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