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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used in the illicit manufacture of narcotic drugs and psychotropic substances 2017 EMBARGO Observe release date: Not to be published or broadcast before Thursday, 1 March 2018, at 1100 hours (CET) UNITED NATIONS CAUTION Reports published by the International Narcotics Control Board in 2017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). -
Pp-03-25-New Dots.Qxd 10/23/02 2:41 PM Page 778
pp-03-25-new dots.qxd 10/23/02 2:41 PM Page 778 778 PRAESODYMIUM PRAESODYMIUM [7440–10–0] Symbol Pr; atomic number 59; atomic weight 140.908; a lanthanide–series rare earth element; belongs to the cerium group of rare earths; electron con- figuration [Xe] 4f36s2; partially filled f subshell; valence states +3, +4; most 3+ stable oxidation state +3; electrode potential E°/V (aq) for Pr + 3e¯ ↔ Pr is –2.35 V; atomic radius 1.828 Å; first ionization potential 5.46 eV; one natu- rally–occurring isotope, Pr–141; twenty–nine artificial radioactive isotopes known in the mass range 124, 126–140 and 142–154; the longest–lived isotope Pr–143, t1/2 13.57 day, and the shortest–lived isotope Pr–124, t1/2 1.2 second. History, Occurrence, and Uses Mosander extracted from the mineral lanthana a rare earth fraction, named didymia in 1841. In 1879, Boisbaudran separated a rare earth oxide called samaria (samarium oxide) from the didymia fraction obtained from the mineral samarskite. Soon after that in 1885, Baron Auer von Welsbach iso- lated two other rare earths from didymia. He named them as praseodymia (green twin) and neodymia (new twin) after their source didymia (twin). The name praseodymium finally was assigned to this new element, derived from the two Greek words, prasios meaning green and didymos meaning twin. Praseodymium occurs in nature associated with other rare earths in a rel- atively high abundance. It is more abundant than some common metals such as silver, gold, or antimony. The average concentration of this metal in the earth’s crust is estimated to be 8.2 mg/kg. -
The Preparation and Reactions of the Lower Chlorides and Oxychlorides of Silicon Joseph Bradley Quig Iowa State College
Iowa State University Capstones, Theses and Retrospective Theses and Dissertations Dissertations 1926 The preparation and reactions of the lower chlorides and oxychlorides of silicon Joseph Bradley Quig Iowa State College Follow this and additional works at: https://lib.dr.iastate.edu/rtd Part of the Inorganic Chemistry Commons Recommended Citation Quig, Joseph Bradley, "The preparation and reactions of the lower chlorides and oxychlorides of silicon " (1926). Retrospective Theses and Dissertations. 14278. https://lib.dr.iastate.edu/rtd/14278 This Dissertation is brought to you for free and open access by the Iowa State University Capstones, Theses and Dissertations at Iowa State University Digital Repository. It has been accepted for inclusion in Retrospective Theses and Dissertations by an authorized administrator of Iowa State University Digital Repository. For more information, please contact [email protected]. INFORMATION TO USERS This manuscript has been reproduced from the microfilm master. UlVli films the text directly from the original or copy submitted. Thus, some thesis and dissertation copies are in typewriter face, while others may be from any type of computer printer. The quality of this reproduction is dependent upon the quality of the copy submitted. Broken or indistinct print, colored or poor quality illustrations and photographs, print bleedthrough, substandard margins, and impiroper alignment can adversely affect reproduction. In the unlikely event that the author did not send UMI a complete manuscript and there are missing pages, these will be noted. Also, if unauthorized copyright material had to be removed, a note will indicate the deletion. Oversize materials (e.g., maps, drawings, charts) are reproduced by sectioning the original, beginning at the upper left-hand corner and continuing from left to right in equal sections with small overiaps. -
APPENDIX G Acid Dissociation Constants
harxxxxx_App-G.qxd 3/8/10 1:34 PM Page AP11 APPENDIX G Acid Dissociation Constants § ϭ 0.1 M 0 ؍ (Ionic strength ( † ‡ † Name Structure* pKa Ka pKa ϫ Ϫ5 Acetic acid CH3CO2H 4.756 1.75 10 4.56 (ethanoic acid) N ϩ H3 ϫ Ϫ3 Alanine CHCH3 2.344 (CO2H) 4.53 10 2.33 ϫ Ϫ10 9.868 (NH3) 1.36 10 9.71 CO2H ϩ Ϫ5 Aminobenzene NH3 4.601 2.51 ϫ 10 4.64 (aniline) ϪO SNϩ Ϫ4 4-Aminobenzenesulfonic acid 3 H3 3.232 5.86 ϫ 10 3.01 (sulfanilic acid) ϩ NH3 ϫ Ϫ3 2-Aminobenzoic acid 2.08 (CO2H) 8.3 10 2.01 ϫ Ϫ5 (anthranilic acid) 4.96 (NH3) 1.10 10 4.78 CO2H ϩ 2-Aminoethanethiol HSCH2CH2NH3 —— 8.21 (SH) (2-mercaptoethylamine) —— 10.73 (NH3) ϩ ϫ Ϫ10 2-Aminoethanol HOCH2CH2NH3 9.498 3.18 10 9.52 (ethanolamine) O H ϫ Ϫ5 4.70 (NH3) (20°) 2.0 10 4.74 2-Aminophenol Ϫ 9.97 (OH) (20°) 1.05 ϫ 10 10 9.87 ϩ NH3 ϩ ϫ Ϫ10 Ammonia NH4 9.245 5.69 10 9.26 N ϩ H3 N ϩ H2 ϫ Ϫ2 1.823 (CO2H) 1.50 10 2.03 CHCH CH CH NHC ϫ Ϫ9 Arginine 2 2 2 8.991 (NH3) 1.02 10 9.00 NH —— (NH2) —— (12.1) CO2H 2 O Ϫ 2.24 5.8 ϫ 10 3 2.15 Ϫ Arsenic acid HO As OH 6.96 1.10 ϫ 10 7 6.65 Ϫ (hydrogen arsenate) (11.50) 3.2 ϫ 10 12 (11.18) OH ϫ Ϫ10 Arsenious acid As(OH)3 9.29 5.1 10 9.14 (hydrogen arsenite) N ϩ O H3 Asparagine CHCH2CNH2 —— —— 2.16 (CO2H) —— —— 8.73 (NH3) CO2H *Each acid is written in its protonated form. -
United States Patent [19] [11] Patent Number: 5,368,832 Buckholtz Et A1
USOO5368832A United States Patent [19] [11] Patent Number: 5,368,832 Buckholtz et a1. [45] Date of Patent: Nov. 29, 1994 [54] ZERO DISCI'IARGE PRQCESS FOR 4,330,515 5/1982 Campbell .......................... .. 423/316 MANUFACI'URING OF PHOSPHOROUS 4,380,531 4/1983 Wisnouskas ....................... .. 423/316 ACID AND HYPOPHOSPHOROUS ACID FOREIGN PATENT DOCUMENTS [75] 1I1v¢m°rs= HWY E- Buckh‘?tz, Lewiswn; 0007493 2/1980 European Pat. Off. .......... .. 423/317 Mohan S. Saran, Grand Island, both 254166 11/1986 Japan _ Of N.Y.; Frederick C. Leiterf, 7900920 11/1979 WIPO ............................... .. 423/316 Madison; David A. Flautt, Ashtabula, both of Ohio Primary iExaminer-Michael Lewis Assistant Examiner—-Stephen G. Kalinchak [73] Assignee: gggiggg?gg? Corporation’ gltltglrgey, Agent, or Firm-Wayne A. Jones; Richard D. [21] Appl. No.: 711,841 [57] ' ABS Cr [22] Flled' : Jun . 7 ’ 1991 Dlsclosed. 1s. a method of making. phosphorous acid. or [51] Int. Cl.5 .................. .. C01B 25/165; COlB 25/163 hypophosphomus acid by reacting hydrogen chloride U:S. C1. ................................... .. 423/ 316; 423/ 317 with a sodium phosphite or a sodium hypophosphite’ [58] Field of Search ............. .. 423/ 167, 307, 316, 317, respectively, in the presence of water to precipitate 423/321 R sodium chloride crystals and form the acid. The acid is [56] References Cited separated from the sodium chloride crystals and-can be US PATENT DOCUMENTS passed through amon exchange column that 1s pref erably loaded with phosphite or hypophosphite lons, 2,595,198 4/1952 Leffore et a1. ............ .. 423/316 respectively, to remove'residual chloride ions_ 2,711,388 6/1955 Mottern et a1. -
EXTRACTION EQUILIBRIA of HYPOPHOSPHOROUS, PHOSPHOROUS and PHOSPHORIC ACIDS by TOLUENE SOLUTION of TRI-N-OCTYLAMINE
ARS SEPARATORIA AA ACTA Ars Separatoria Acta 2 (2003) 125-138 www.ars_separatoria.chem. uni.torun.pl EXTRACTION EQUILIBRIA OF HYPOPHOSPHOROUS, PHOSPHOROUS AND PHOSPHORIC ACIDS BY TOLUENE SOLUTION OF TRI-n-OCTYLAMINE Takashi SANA2, Koichiro SHIOMORI1, and Yoshinobu KAWANO1* 1 Department of Applied Chemistry, Miyazaki Univ., Miyazaki 889-2192, Japan e-mail: [email protected] 2 Yoshitama Surface Finishing Co., LTD, Nobeoka 882-0024, Japan ABSTRACT The extraction equilibria of hypophosphorous, phosphorous and phosphoric acids with tri-n-octylamine as an extractant in toluene were measured at 303K. Under these conditions, undissociated acid (A') reacts with the amine (B) to form various complexes in toluene. The complexes formed and equilibrium constants were estimated by a graphical analysis method. The complexes formed in these systems were found to be A'nB type species for hypophosphorous acid, A'nBm type species for phosphorous acid, (A'B)n type species for phosphoric acid, respectively. The experimental results could be explained by reaction models and equilibrium constants for each acid. Keywords: Hypophosphorous acid; Phosphorous acid; Phosphoric acid; Tri-n-octylamine; Extraction equilibrium INTRODUCTION Solvent extraction gives the advantage of selective separation in the recycling of useful materials [1,2]. The nonelectrolytic nickel-plating wastewater consists of nickel, some organic acids, hypophosphorous acid, phosphorous acid, and phosphoric acid. In order to design a new wastewater treatment equipment of nonelectrolytic nickel-plating, it is necessary to clarify the extraction equilibrium and kinetics for each component contained in wastewater. For that fundamental knowledge, the extraction equilibrium and kinetic for nickel with 5-dodecylsalicylaldoxime [3,4] as well as * Corresponding author 125 Sana, et.al. -
(12) Patent Application Publication (10) Pub. No.: US 2008/0103330 A1 Liu Et Al
US 20080 103330A1 (19) United States (12) Patent Application Publication (10) Pub. No.: US 2008/0103330 A1 Liu et al. (43) Pub. Date: May 1, 2008 (54) PROCESS FOR THE PREPARATION OF Publication Classification HIGHLY PURIFIED, (51) Int. Cl. DALKYDTHOPHOSPHINC COMPOUNDS C07F 9/30 (2006.01) C07F 9/34 (2006.01) (76) Inventors: Leo Zhaoqing Liu, Shanghai (CN); (52) U.S. Cl. ............................................... 562/9:568/14 Gary Woodward, Northwich (57) ABSTRACT Cheshire (GB) An improved process for production of dialkyldithiophos phinic acid including Sulfurizing a purified dialkylphosphinic Correspondence Address: acid by: reacting a hypophosphorous acid or salt with a sto Kevin E. McVeigh ichiometric excess of an alpha olefin in the presence of a free RHODANC. radical initiator to form a reaction product comprising 8 Cedar Brook Drive monoalkylphosphinic acid and dialkylphosphinic acid; add Cranbury, NJ 08512-7500 ing Sufficient aqueous base to the reaction product to i) form the salts of the phosphinic acids, and ii) establish an aqueous phase and an organic phase, wherein a monoalkylphosphinic (21) Appl. No.: 11/977,620 acid solubilizes into an aqueous phase; separating the organic phase from the aqueous phase; acidifying the organic phase (22) Filed: Oct. 25, 2007 and removing the olefin from the organic phase; isolating the purified dialkylphosphinic acid product; and Sulfurizing the Related U.S. Application Data purified dialkylphosphinic acid product to form a dialky dithiophosphinic acid. The present invention also provides a (60) Provisional application No. 60/854.279, filed on Oct. process for preparing purified dialkylthiophosphinic chlo 25, 2006, provisional application No. 60/914,558, ride, and a process for preparing purified dialkylmonothio filed on Apr. -
(12) Patent Application Publication (10) Pub. No.: US 2016/0115593 A1 KUCHENBESER Et Al
US 2016O115593A1 (19) United States (12) Patent Application Publication (10) Pub. No.: US 2016/0115593 A1 KUCHENBESER et al. (43) Pub. Date: Apr. 28, 2016 (54) AMINO(IODO)SILANE PRECURSORS FOR HOIL 2/3 II (2006.01) ALDACVD SILICON-CONTAINING FILM C23C I6/34 (2006.01) APPLICATIONS AND METHODS OF USING C23C I6/56 (2006.01) THE SAME (52) U.S. Cl. CPC ......... C23C 16/45553 (2013.01); C23C 16/345 (71) Applicant: American Air Liquide, Inc., Fremont, (2013.01); C23C I6/45536 (2013.01); C23C CA (US) I6/56 (2013.01); HOIL 21/31 III (2013.01); HOIL 21/02211 (2013.01); HOIL 21/02274 (72) Inventors: Glenn KUCHENBEISER, Newark, DE (2013.01); HOIL 2L/0228 (2013.01); HOIL (US); Bastien LEFEVRE, Wilmington, 21/0217 (2013.01) DE (US) (21) Appl. No.: 14/984,866 (57) ABSTRACT (22) Filed: Dec. 30, 2015 Publication Classification Disclosed are amino(iodo)silane precursors, methods of syn thesizing the same, and methods of using the same to deposit (51) Int. Cl. silicon-containing films using vapor deposition processes. C23C I6/455 (2006.01) The disclosed amino(iodo)silane precursors include SiHI(N HOIL 21/02 (2006.01) (iPr)) or SiHI(N(iBu)). Patent Application Publication Apr. 28, 2016 Sheet 1 of 6 US 2016/O115593 A1 FG Patent Application Publication Apr. 28, 2016 Sheet 2 of 6 US 2016/O115593 A1 100 T - - - - 90 - SiH(NMe2)2 atmoc 44mg 80 - - - - SiH(NMe2)2 closed cup 70 - 50 - 30 - 10 - O 1 OO 2OO 300 400 500 Temperature (°C) FIG. 3 - - SiH2(NEt2) atmoc 41 mg SiH2(NEt2) closed Cup 22mg s s cus s 9 CD 8 300 Temperature (°C) FIG. -
Dec. 12, 1961 H
Dec. 12, 1961 H. W. LNG 3,012,861 PRODUCTION OF SILICON Filed Jan. 15, 1960 zzzzz INVENTOR HARRY W. LING ATTORNEY 3,012,861 United States Patent Office Patented Dec. 12, 1961 1. 2 3,012,861 . Referring now to this drawing, there is shown a ver PRODUCTION OF SELICON tically disposed cylindrical or tubular reactor 1 with a Harry W. Ling, Wilmington, Del assignor to E. I. du conical bottom 3 provided with inlet 4 for entrance of Pont de Nemours and Company, Wilmington, Dei, a reactant fluidizing gas. The reactor 1 is sufficiently high corporation of Delaware to provide for a 2-3 times expansion of the bed 6 and also Filed Jan. 15, 1960, Ser. No. 3,708. a disengaging space 7 above the bed 6 to reduce solids 9. Claims. (C. 23-223.5) blowover to a minimum. A valved inlet 8 is provided for introduction of silicon bed particles. The reaction This invention relates to the production of elemental by-product gases are removed from the reactor through silicon. More particularly, it relates to a new and im 10 the outlet 9 and cyclone 13 which can be kept hot by a proved method of thermally decomposing volatile silicon furnace (not shown). These gases then pass to a con compounds. densing system 10 and cold trap (not shown) through Silicon can be produced by thermally decomposing sili which the vacuum pumping system (not shown) is con con iodide at a reduced pressure -on an electrically nected. The reactor 1 is maintained at the desired reactor heated, incandescent metal filament. -
Nitrous Acid)
5. Nitrogen Group Content 5.1 Occurrence 5.2 Group Properties Group 5.3 Physical Properties 15 or VA 5.4 Syntheses 7 1772 5.5 Chemical Behaviour N 15 5.6 Applications 1669 5.7 Chemistry of Elemental Nitrogen P 33 5.8 Compounds Made of Nitrogen and Hydrogen Antique 5.9 Nitrogen Compounds with Oxygen As 51 5.10 Nitrogen Compounds with Halides Antique Sb 5.11 Phosphorus/Hydrogen Compounds 83 1753 5.12 Phosphorus Oxides Bi 5.13 Oxo Acids of Phosphorus 115 2003 5.14 Phosphorus Compounds with Halides Mc 5.15 Arsenic, Antimony and Bismuth 5.16 Biological Aspects „Penteles“ Inorganic Chemistry I Slide 1 Prof. Dr. T. Jüstel 5.1 Occurrence Außer Phosphor kommen alle Pentele auch elementar (gediegen) vor Nitrogen (nitrogenium) N2 (78.1% in the air) NaNO3 Chile saltpetre KNO3 Saltpetre Phosphorus (phosphoros) Ca5(PO4)3(OH,F) Apatite greek: lightbearer Ca3(PO4)2 Phosphorite . Fe3(PO4)2 8H2O Vivianite Arsenic (arsenikos) FeAsS Arsenopyrite greek: mineral name As4S4 Realgar As4S3 Antimony (antimonium) Sb native Stibium = greek mineral name Sb2S3 Bismuth (bismutum) Bi native german: Wismut = Mutung “in the meadows” Bi2S3 Inorganic Chemistry I Slide 2 Prof. Dr. T. Jüstel 5.2 Group Properties Whereas Nitrogen Exhibits the Typical Properties of A Non-Metal, Bismuth Is Solely Metallic N P As Sb Bi Atomic number 7 15 33 51 83 Electronic [He] [Ne] [Ar] [Kr] [Xe]4f14 configuration 2s22p3 3s23p3 3d104s24p3 4d105s25p3 5d106s26p3 Electronegativity 3.0 2.1 2.2 1.8 1.7 Ionisation energy [eV] 14.5 11.0 9.8 8.6 7.3 Electronic affinity [eV] -0.3 0.6 0.7 0.6 > 0.7 Character of oxides acidic acidic amphoteric amphoteric alkaline Oxidation states -3, ...…, +5 With increasing atomic number, the oxidation state +3 becomes more stable, whilst the oxidation state +5 becomes instable. -
United States Patent Office Patented Aug
3,832,364 United States Patent Office Patented Aug. 27, 1974. 2 zene, o-, m- and p-dichlorobenzene, anisole, methyl. 3,832,364 benzyl ether, n-propyl phenyl ether, m-ethyl-anisole, 4 AMINATION OF AROMATIC COMPOUNDS IN methyldiphenyl ether, di-p-tolyl ether, ethyl 2-cyclohexyl LIQUID HYDROGEN FLUORIDE Dale Robert Coulson, Wilmington, Del assignor to E. I. phenyl ether, n-heptyl phenyl ether, isobutyl phenyl ether, du Pont de Nemours and Company, Wilmington, Del. 5 cyclohexyl phenyl ether, n-octyl phenyl ether, n-octyl p No Drawing. Filed May 25, 1972, Ser. No. 256,770 tolyl ether, n-octyl m-tolyl ether, decyl phenyl ether, 1 Int. C. C07c87/50, 97/12 benzylethylheptyl ether, benzoic acid, p-toluic acid, p U.S. C. 260-378 26 Claims chlorobenzoic acid, phthalic acid, nitrobenzene, m-dinitro benzene, o-, m- and p-nitrotoluene, acetophenone, methyl O benzyl ketone, p-methylacetophenone, 3-phenyl-2-buta ABSTRACT OF THE DISCLOSURE none, propriophenone, 2-methyl-1-tetralone, phenyl. n Disclosed herein is a process for making aromatic butyl ketone, benzophenone, p-methylbenzophenone, di amines from benzene or substituted benzene and an o-tolyl ketone, phenyl isobutyl ketone, phenyl n-hexyl aminating agent via direct amination in liquid hydrogen ketone, phenyl n - undecyl ketone, anthraquinone, 2 - fluoride medium as solvent and catalyst. 15 methylanthraquinone, and 1-methyl-4-isopropylanthra quinone. Preferred aromatic compounds are those containing BACKGROUND OF THE INVENTION two or fewer substituents. Especially preferred com 1. Field of the Invention pounds are those containing two or fewer substituents 20 selected from halogen and alkyl of up to four carbons. -
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.