An Expanding Synthetic Drugs Market − Implications for Precursor Control EN
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Precursors and Chemicals Frequently Used in the Illicit Manufacture of Narcotic Drugs and Psychotropic Substances 2017
INTERNATIONAL NARCOTICS CONTROL BOARD Precursors and chemicals frequently used in the illicit manufacture of narcotic drugs and psychotropic substances 2017 EMBARGO Observe release date: Not to be published or broadcast before Thursday, 1 March 2018, at 1100 hours (CET) UNITED NATIONS CAUTION Reports published by the International Narcotics Control Board in 2017 The Report of the International Narcotics Control Board for 2017 (E/INCB/2017/1) is supplemented by the following reports: Narcotic Drugs: Estimated World Requirements for 2018—Statistics for 2016 (E/INCB/2017/2) Psychotropic Substances: Statistics for 2016—Assessments of Annual Medical and Scientific Requirements for Substances in Schedules II, III and IV of the Convention on Psychotropic Substances of 1971 (E/INCB/2017/3) Precursors and Chemicals Frequently Used in the Illicit Manufacture of Narcotic Drugs and Psychotropic Substances: Report of the International Narcotics Control Board for 2017 on the Implementation of Article 12 of the United Nations Convention against Illicit Traffic in Narcotic Drugs and Psychotropic Substances of 1988 (E/INCB/2017/4) The updated lists of substances under international control, comprising narcotic drugs, psychotropic substances and substances frequently used in the illicit manufacture of narcotic drugs and psychotropic substances, are contained in the latest editions of the annexes to the statistical forms (“Yellow List”, “Green List” and “Red List”), which are also issued by the Board. Contacting the International Narcotics Control Board The secretariat of the Board may be reached at the following address: Vienna International Centre Room E-1339 P.O. Box 500 1400 Vienna Austria In addition, the following may be used to contact the secretariat: Telephone: (+43-1) 26060 Fax: (+43-1) 26060-5867 or 26060-5868 Email: [email protected] The text of the present report is also available on the website of the Board (www.incb.org). -
COMBINED LIST of Particularly Hazardous Substances
COMBINED LIST of Particularly Hazardous Substances revised 2/4/2021 IARC list 1 are Carcinogenic to humans list compiled by Hector Acuna, UCSB IARC list Group 2A Probably carcinogenic to humans IARC list Group 2B Possibly carcinogenic to humans If any of the chemicals listed below are used in your research then complete a Standard Operating Procedure (SOP) for the product as described in the Chemical Hygiene Plan. Prop 65 known to cause cancer or reproductive toxicity Material(s) not on the list does not preclude one from completing an SOP. Other extremely toxic chemicals KNOWN Carcinogens from National Toxicology Program (NTP) or other high hazards will require the development of an SOP. Red= added in 2020 or status change Reasonably Anticipated NTP EPA Haz list COMBINED LIST of Particularly Hazardous Substances CAS Source from where the material is listed. 6,9-Methano-2,4,3-benzodioxathiepin, 6,7,8,9,10,10- hexachloro-1,5,5a,6,9,9a-hexahydro-, 3-oxide Acutely Toxic Methanimidamide, N,N-dimethyl-N'-[2-methyl-4-[[(methylamino)carbonyl]oxy]phenyl]- Acutely Toxic 1-(2-Chloroethyl)-3-(4-methylcyclohexyl)-1-nitrosourea (Methyl-CCNU) Prop 65 KNOWN Carcinogens NTP 1-(2-Chloroethyl)-3-cyclohexyl-1-nitrosourea (CCNU) IARC list Group 2A Reasonably Anticipated NTP 1-(2-Chloroethyl)-3-cyclohexyl-1-nitrosourea (CCNU) (Lomustine) Prop 65 1-(o-Chlorophenyl)thiourea Acutely Toxic 1,1,1,2-Tetrachloroethane IARC list Group 2B 1,1,2,2-Tetrachloroethane Prop 65 IARC list Group 2B 1,1-Dichloro-2,2-bis(p -chloropheny)ethylene (DDE) Prop 65 1,1-Dichloroethane -
A Study of the Intermediate Steps in the Preparation of Alkylphenylbarbituric Acids James Edward Doyle University of Massachusetts Amherst
University of Massachusetts Amherst ScholarWorks@UMass Amherst Masters Theses 1911 - February 2014 1933 A study of the intermediate steps in the preparation of alkylphenylbarbituric acids James Edward Doyle University of Massachusetts Amherst Follow this and additional works at: https://scholarworks.umass.edu/theses Doyle, James Edward, "A study of the intermediate steps in the preparation of alkylphenylbarbituric acids" (1933). Masters Theses 1911 - February 2014. 1468. Retrieved from https://scholarworks.umass.edu/theses/1468 This thesis is brought to you for free and open access by ScholarWorks@UMass Amherst. It has been accepted for inclusion in Masters Theses 1911 - February 2014 by an authorized administrator of ScholarWorks@UMass Amherst. For more information, please contact [email protected]. A STUDY OF THE INTERMEDIATE STEPS IN THE PREPARATION OF ALKYLPHENYLBARBITURIC ACIDS JAMES EDWARD DOYLE Thesis submitted for the degree of Master of Science MASSACHUSETTS STATE COLLEGE June 1933 TABLE OF CONTENTS Page I. INTRODUCTION 1 II. THEORY AND REVIEW OF LITERATURE 2 A. Abstracts of Patents 2 B. Previous Work on Luminal 5 C. Reactions 9 D. Previous Work on Cyanophenylacetic Acid ll*. E f Previous Work on 5»5-Isopropylphenyl- barbituric Acid 17 III. EXPERIMENTAL WORK 19 A. Preparation of Luminal 19 1. Benzyl Cyanide 21 2. Ethyl Cyanophenylacetate 22 3. Ethyl Cyanoethylphenylacetate 2l\. 5,5-Sthylphenyl-^-iminobarbituric Acid25 5. 5,5-Ethylphenylbarbituric Acid 27 B. Preparation of Ethyl oc ,-f-Dicyano-oc ,f« diphenylacetoacetate 27 1. Ethyl oc ,-Y-Dicyano-cc ,v -diphenyl- acetoacetate 29 2. Ethyl y-Cyano-oc ,Y -diphenylacetoacetate 3 2 C. Preparation of Cyanophenylacetic Acid 3k 1. -
Benzyl Chlorid Final
Survey of benzyl chloride (CAS no. 100-44-7) Part of the LOUS-review [Series Title and year] Consultation draft Title: Editing: Survey of benzyl chloride (CAS no. 100-44-7) Pia Brunn Poulsen, FORCE Technology Maria Strandesen, FORCE Technology Anders Schmidt, FORCE Technology Published by: Photography: The Danish Environmental Protection Agency [Name] Strandgade 29 1401 Copenhagen K Denmark Illustration: www.mst.dk/english [Name] Year: Map: [xxxx] [Name] ISBN no. [xxxxxx] Disclaimer: When the occasion arises, the Danish Environmental Protection Agency will publish reports and papers concerning research and development projects within the environmental sector, financed by study grants provided by the Danish Environmental Protection Agency. It should be noted that such publications do not necessarily reflect the position or opinion of the Danish Environmental Protection Agency. However, publication does indicate that, in the opinion of the Danish Environmental Protection Agency, the content represents an important contribution to the debate surrounding Danish environmental policy. While the information provided in this report is believed to be accurate, The Danish Environmental Protection Agency disclaims any responsibility for possible inaccuracies or omissions and consequences that may flow from them. Neither the Danish Environmental Protection Agency nor FORCE Technology or any individual involved in the preparation of this publication shall be liable for any injury, loss, damage or prejudice of any kind that may be caused by persons who have acted based on their understanding of the information contained in this publication. Sources must be acknowledged. 2 Survey of benzyl chloride (CAS no. 100-44-7) Contents Preface ...................................................................................................................... 6 Summary and conclusions ......................................................................................... 8 Sammenfatning og konklusion ............................................................................... -
Safe Handling and Disposal of Chemicals Used in the Illicit Manufacture of Drugs
Vienna International Centre, PO Box 500, 1400 Vienna, Austria Tel.: (+43-1) 26060-0, Fax: (+43-1) 26060-5866, www.unodc.org Guidelines for the Safe handling and disposal of chemicals used in the illicit manufacture of drugs United Nations publication USD 26 Printed in Austria ISBN 978-92-1-148266-9 Sales No. E.11.XI.14 ST/NAR/36/Rev.1 V.11-83777—September*1183777* 2011—300 Guidelines for the Safe handling and disposal of chemicals used in the illlicit manufacture of drugs UNITED NATIONS New York, 2011 Symbols of United Nations documents are composed of letters combined with figures. Mention of such symbols indicates a reference to a United Nations document. ST/NAR/36/Rev.1 UNITED NATIONS PUBLICATION Sales No. E.11.XI.14 ISBN 978-92-1-148266-9 eISBN 978-92-1-055160-1 © United Nations, September 2011. All rights reserved. The designations employed and the presentation of material in this publication do not imply the expression of any opinion whatsoever on the part of the Secretariat of the United Nations concerning the legal status of any country, territory, city or area, or of its authorities, or concerning the delimitation of its frontiers or boundaries. Requests for permission to reproduce this work are welcomed and should be sent to the Secretary of the Publications Board, United Nations Headquarters, New York, N.Y. 10017, U.S.A. or also see the website of the Board: https://unp.un.org/Rights.aspx. Governments and their institutions may reproduce this work without prior authoriza- tion but are requested to mention the source and inform the United Nations of such reproduction. -
Metabolic Engineering of Escherichia Coli to High Efficient Synthesis
Zhang et al. AMB Expr (2017) 7:105 DOI 10.1186/s13568-017-0407-0 ORIGINAL ARTICLE Open Access Metabolic engineering of Escherichia coli to high efcient synthesis phenylacetic acid from phenylalanine Lihua Zhang1,2, Qian Liu1,2, Hong Pan2*, Xun Li2 and Daoyi Guo1,2* Abstract Phenylacetic acid (PAA) is a fne chemical with a high industrial demand for its widespread uses. Whereas, microor- ganic synthesis of PAA is impeded by the formation of by-product phenethyl alcohol due to quick, endogenous, and superfuous conversion of aldehydes to their corresponding alcohols, which resulted in less conversation of PAA from aldehydes. In this study, an Escherichia coli K-12 MG1655 strain with reduced aromatic aldehyde reduction (RARE) that does duty for a platform for aromatic aldehyde biosynthesis was used to prompt more PAA biosynthesis. We establish a microbial biosynthetic pathway for PAA production from the simple substrate phenylalanine in E. coli with heterolo- gous coexpression of aminotransferase (ARO8), keto acid decarboxylase (KDC) and aldehyde dehydrogenase H (AldH) gene. It was found that PAA transformation yield was up to ~94% from phenylalanine in E. coli and there was no by-product phenethyl alcohol was detected. Our results reveal the high efciency of the RARE strain for production of PAA and indicate the potential industrial applicability of this microbial platform for PAA biosynthesis. Keywords: Metabolic engineering, Phenylacetic acid, Phenylalanine, Phenylacetaldehyde Introduction utilizing a nitrile hydratase and an amidase of Rhodococ- Phenylacetic acid (PAA) has received much attention on cus equi TG328 (Gilligan et al. 1993) or an arylacetoni- account of its extensive applications, which ofer the huge trilase from Pseudomonas fuorescens EBC191 (Sosedov demand. -
Quantifying the Origins of Life on a Planetary Scale
Quantifying the origins of life on a planetary scale Caleb Scharfa,1 and Leroy Croninb,1 aColumbia Astrobiology Center, Columbia Astrophysics Laboratory, New York, NY 10027; and bSchool of Chemistry, University of Glasgow, Glasgow, G12 8QQ, United Kingdom Edited by Neta A. Bahcall, Princeton University, Princeton, NJ, and approved May 17, 2016 (received for review November 23, 2015) A simple, heuristic formula with parallels to the Drake Equation is currently impossible to construct a first principles quantitative introduced to help focus discussion on open questions for the origins estimate of an abiogenesis probability for the young Earth. It is of life in a planetary context. This approach indicates a number of also the case that we typically conflate the idea of “microabio- areas where quantitative progress can be made on parameter genesis”— namely, a highly localized assembly of molecular estimation for determining origins of life probabilities, based on structures that meets the minimum criterion for a living system— constraints from Bayesian approaches. We discuss a variety of “micro- with “macro-” or planet-wide abiogenesis. In other words the idea scale” factors and their role in determining “macroscale” abiogenesis of life arising on a planet is treated as a singular event rather than probabilities on suitable planets. We also propose that impact ejecta a possible accumulation of many microscale events, each of which exchange between planets with parallel chemistries and chemical evo- might be considered an origin event in its own right, and are ar- lution could in principle amplify the development of molecular com- guably more accessible through laboratory or modeling investi- plexity and abiogenesis probabilities. -
Identification of Substance P Precursor Forms in Human Brain Tissue
Proc. Nati. Acad. Sci. USA Vol. 82, pp. 3921-3924, June 1985 Neurobiology Identification of substance P precursor forms in human brain tissue (prohormones/tachykinins/hypothalamus/substantia nigra/caudate nucleus) FRED NYBERG, PIERRE LE GREvls, AND LARS TERENIUS Department of Pharmacology, University of Uppsala, S-751 24 Uppsala, Sweden Communicated by Tomas Hokfelt, January 28, 1985 ABSTRACT Substance P prohormones were identified in glycine (19). Enzymes involved in the processing of the the caudate nucleus, hypothalamus, and substantia nigra of precursors are incompletely known. human brain. A polypeptide fraction of acidic brain extracts The present paper reports the identification of substance P was fractionated on Sephadex G-50. The Iyophilized fractions precursors in human brain. The strategy for the experimental were sequentially treated with trypsin and a substance P- approach is based on the enzymatic generation in vitro of a degrading enzyme with strong preference toward the Phe7- unique peptide fragment (20, 21). Trypsin treatment of any Phe' and Phe8-Gly9 bonds. The released substance P(1-7) product of the preprotachykinins containing the substance P fragment was isolated by ion-exchange chromatography and sequence generates a fragment with the NH2-terminal region quantitated by a specific radioimmunoassay. Confirmation of identical with that of the native peptide. Further conversion the structure of the isolated radioimmunoassay-active frag- of this fragment with an endopeptidase capable of hydrolyz- ment was achieved by electrophoresis and HPLC. By using this ing substance P at the Phe7-Phe8 bond releases the substance enzymatic/radioimmunoassay procedure, two polypeptide P(1-7) sequence as a fragment that can be recovered by fractions of apparent M, 5000 and 15,000, respectively, were ion-exchange chromatography and quantitated by a specific identified. -
The Dissipative Photochemical Origin of Life: UVC Abiogenesis of Adenine
entropy Article The Dissipative Photochemical Origin of Life: UVC Abiogenesis of Adenine Karo Michaelian Department of Nuclear Physics and Applications of Radiation, Instituto de Física, Universidad Nacional Autónoma de México, Circuito Interior de la Investigación Científica, Cuidad Universitaria, Mexico City, C.P. 04510, Mexico; karo@fisica.unam.mx Abstract: The non-equilibrium thermodynamics and the photochemical reaction mechanisms are described which may have been involved in the dissipative structuring, proliferation and complex- ation of the fundamental molecules of life from simpler and more common precursors under the UVC photon flux prevalent at the Earth’s surface at the origin of life. Dissipative structuring of the fundamental molecules is evidenced by their strong and broad wavelength absorption bands in the UVC and rapid radiationless deexcitation. Proliferation arises from the auto- and cross-catalytic nature of the intermediate products. Inherent non-linearity gives rise to numerous stationary states permitting the system to evolve, on amplification of a fluctuation, towards concentration profiles providing generally greater photon dissipation through a thermodynamic selection of dissipative efficacy. An example is given of photochemical dissipative abiogenesis of adenine from the precursor HCN in water solvent within a fatty acid vesicle floating on a hot ocean surface and driven far from equilibrium by the incident UVC light. The kinetic equations for the photochemical reactions with diffusion are resolved under different environmental conditions and the results analyzed within the framework of non-linear Classical Irreversible Thermodynamic theory. Keywords: origin of life; dissipative structuring; prebiotic chemistry; abiogenesis; adenine; organic molecules; non-equilibrium thermodynamics; photochemical reactions Citation: Michaelian, K. The Dissipative Photochemical Origin of MSC: 92-10; 92C05; 92C15; 92C40; 92C45; 80Axx; 82Cxx Life: UVC Abiogenesis of Adenine. -
Precursors and Chemicals Frequently Used in the Illicit Manufacture Of
III. EXTENT OF Licit traDE AND Latest trenDS IN traFFICKING IN precursors 13 70. INCB wishes to reiterate the importance of substances and on shipments of substances that have engaging relevant sectors of industry to ensure the been stopped on the basis of sufficient evidence that successful and sustainable prevention of chemical the substances may have been diverted into illicit diversion. INCB also wishes to reiterate that, although channels, is essential to addressing emerging traf- determining the nature and extent of such cooperation ficking trends at an early stage and globally. INCB is the prerogative of individual countries, it is impor- also wishes to remind Governments that thwarted tant that competent national authorities share attempts to divert a given substance should receive information about suspicious requests, orders and the same investigative attention that would be transactions with INCB in order to prevent “company afforded to a seizure of the same substance, since shopping”, i.e., the shifting from one supplier to such cases provide valuable intelligence that, if another, across borders. shared internationally, could prevent attempts to divert the substances from other sources. 4. Tracking of precursor chemicals to prevent their diversion A. Substances used in the illicit 71. In response to Commission on Narcotic Drugs manufacture of amphetamine- resolution 62/1, entitled “Strengthening international type stimulants cooperation and comprehensive regulatory and institu- tional frameworks for the control of precursors used in the 1. Substances used in the illicit illicit manufacture of narcotic drugs and psychotropic manufacture of amphetamines substances”, INCB, in cooperation with the Government of Turkey, convened an expert working group to explore the (a) Ephedrine and pseudoephedrine possibility, practicability and effectiveness of innovative methods to track precursor chemicals, in particular acetic 74. -
Chapter Five, Part D (Supervised Release)
November 1, 2014 GUIDELINES MANUAL §2D1.1 PART D - OFFENSES INVOLVING DRUGS AND NARCO-TERRORISM Historical Note: Effective November 1, 1987. Amended effective November 1, 2007 (see Appendix C, amendment 711). 1. UNLAWFUL MANUFACTURING, IMPORTING, EXPORTING, TRAFFICKING, OR POSSESSION; CONTINUING CRIMINAL ENTERPRISE §2D1.1. Unlawful Manufacturing, Importing, Exporting, or Trafficking (Including Possession with Intent to Commit These Offenses); Attempt or Conspiracy (a) Base Offense Level (Apply the greatest): (1) 43, if the defendant is convicted under 21 U.S.C. § 841(b)(1)(A), (b)(1)(B), or (b)(1)(C), or 21 U.S.C. § 960(b)(1), (b)(2), or (b)(3), and the offense of conviction establishes that death or serious bodily injury resulted from the use of the substance and that the defendant committed the offense after one or more prior convictions for a similar offense; or (2) 38, if the defendant is convicted under 21 U.S.C. § 841(b)(1)(A), (b)(1)(B), or (b)(1)(C), or 21 U.S.C. § 960(b)(1), (b)(2), or (b)(3), and the offense of conviction establishes that death or serious bodily injury resulted from the use of the substance; or (3) 30, if the defendant is convicted under 21 U.S.C. § 841(b)(1)(E) or 21 U.S.C. § 960(b)(5), and the offense of conviction establishes that death or serious bodily injury resulted from the use of the substance and that the defendant committed the offense after one or more prior convictions for a similar offense; or (4) 26, if the defendant is convicted under 21 U.S.C. -
Chapter Five, Part D (Supervised Release)
PART D - OFFENSES INVOLVING DRUGS 1. UNLAWFUL MANUFACTURING, IMPORTING, EXPORTING, TRAFFICKING, OR POSSESSION; CONTINUING CRIMINAL ENTERPRISE §2D1.1. Unlawful Manufacturing. Importing. Exporting, or Trafficking (Including Possession with Intent to Commit These Offenses); Attempt or Conspiracy (a) Base Offense Level (Apply the greatest): (1) 43, if the defendant is convicted under 21 U.S.C. § 841(b)(l)(A), (b)(l)(B), or (b)(l)(C), or 21 U.S.C. § 960(b)(l), (b)(2), or (b)(3), and the offense of conviction establishes that death or serious bodily injury resulted from the use of the substance and that the defendant committed the offense after one or more prior convictions for a similar offense; or (2) 38, if the defendant is convicted under 21 U.S.C. § 841(b)(l)(A), (b)(l)(B), or (b)(l)(C), or 21 U.S.C. § 960(b)(l), (b)(2), or (b)(3), and the offense of conviction establishes that death or serious bodily injury resulted from the use of the substance; or (3) the offense level specified in the Drug Quantity Table set forth in subsection (c) below. (b) Specific Offense Characteristics (1) If a dangerous weapon (including a firearm) was possessed, increase by 2 levels. (2) If the defendant unlawfully imported or exported a controlled substance under circumstances in which (A) an aircraft other than a regularly scheduled commercial air carrier was used to import or export the controlled substance, or (B) the defendant acted as a pilot, copilot, captain, navigator, flight officer, or any other operation officer aboard any craft or vessel carrying a controlled substance, increase by 2 levels.