Technical Secretariat

Total Page:16

File Type:pdf, Size:1020Kb

Technical Secretariat OPCW Technical Secretariat Verification Division S/634/2007 28 March 2007 ENGLISH only REPORT OF THE TWENTY-FIFTH MEETING OF THE VALIDATION GROUP FOR THE UPDATING OF THE OPCW CENTRAL ANALYTICAL DATABASE 27 AND 28 MARCH 2007 1. The Validation Group (hereinafter “the Group”) met for the 25th time on 27 and 28 March 2007 to discuss the evaluation of new analytical data for possible inclusion in the OPCW Central Analytical Database (OCAD), and to consider related matters. Mr Hugh Gregg of the United States of America chaired the Meeting. 2. The evaluators for the analytical techniques evaluated new data and sent their written reports to the coordinators for each analytical technique. The table below lists the names of the coordinators who were present at the Meeting, along with the technique for which each is responsible. Technique Coordinator Mass spectrometry (MS) Mr Edward White (United States of America) Gas chromatography (retention Mr Martin Söderström (Finland) index) GC(RI) Infrared (IR) spectrometry Mr Colin Pottage (United Kingdom of Great Britain and Northern Ireland) 3. These coordinators provided an evaluation summary to the Group for discussion at the Meeting. The evaluators finalised the evaluation of the analytical data and confirmed that the approved data are technically valid. 4. The Group forwarded lists of the validated analytical data to the Director-General for appropriate action (see Annexes 1 and 2). 5. The Technical Secretariat (hereinafter “the Secretariat”) requested that the Group discuss the data on several chemicals, already in the OCAD, that are neither from scheduled chemicals nor are they analytical derivatives of scheduled chemicals. The Group recommends that the Secretariat seek further guidance on the possible inclusion in the OCAD of data on non-scheduled chemicals that may be relevant in the analysis of chemical weapons-related samples. The Group recognised that technically valid data of some non-scheduled chemicals are already included in the OCAD (see Annex 3). CS-2007-5124(E) distributed 20/04/2007 *CS-2007-5124.E* S/634/2007 page 2 6. The Group, after obtaining more information regarding IR spectrum 04-1-0242v, which was initially evaluated at the 23rd meeting of the Group, recommends that this spectrum now be accepted. 7. The Secretariat reported that the decision concerning data on scheduled chemicals, submitted to the Executive Council (hereinafter “the Council”) at its Forty-Eighth Session, was postponed to the next Session. 8. The Secretariat reported that the PDF Version 10 (Electronic Version 8) of the OCAD should be ready for release by the end of 2007. 9. The Secretariat informed the Group that the OCAD project involving the creation of a relational database is ongoing, and that work is continuing on the creation of a working database that contains analytical data on relevant non-scheduled chemicals. The Group will also request that the Secretariat submit this database to the Group’s coordinators as part of the authentication process. 10. The naming rules for several analytical derivatives of lewisites (Schedule 1.A.05) were discussed, and names for specific analytical derivatives of lewisites were established. The “Rules for Naming Compounds in the OPCW Central Analytical Database” were updated (see Annex 4, paragraph 2.13). 11. Following the discussion on this matter that took place at the Ninth Meeting of the Scientific Advisory Board (subparagraph 3.3(c) of SAB-9/1, dated 14 February 2007), the Group discussed the possibility of establishing a liquid chromatography-mass spectrometry (LC-MS) database for potential inclusion in the OCAD. Mr Martin Söderström agreed to lead an effort to poll several laboratories and create a proposal for the Group to consider at its next Meeting. 12. The following analytical data are available for evaluation: MS 16-2-0028 to 16-2-0059, 04-2-0071, 07-2-1930, 07-2-1931, 07-2-2385, 18-2-0073, 07-2-2350 GC(RI) 16-4-0067 to 16-4-0095 13. Additional data are expected for nuclear magnetic resonance spectrometry (NMR), MS, GC(RI), and IR. 14. The Group appointed evaluators for the analytical techniques. Annex 5 to this report lists the evaluators by analytical technique. The evaluators agreed to send their written evaluation reports to the appointed coordinators no later than 4 September 2007. The coordinators agreed to send evaluation summary reports to the Group’s Chairperson and to the evaluators no later than 11 September 2007, so that the reports can be discussed at the Group’s next Meeting, which is scheduled for 18 and 19 September 2007. The evaluators agreed to come to that meeting prepared to finalise the evaluation of the analytical data referred to in paragraphs 12 and 13. 15. The Group would like to welcome Mr R. S. Verma (India) as the new evaluator for MS data. S/634/2007 page 3 Annexes: Annex 1: List of Approved Data Recommended for Inclusion in the OPCW Central Analytical Database Annex 2: List of Technically Valid Data Not Recommended for Inclusion in the OPCW Central Analytical Database Annex 3: Non-scheduled Chemicals in the OPCW Central Analytical Database Annex 4: Rules for Naming Compounds in the OPCW Central Analytical Database Annex 5: List of Evaluators by Analytical Technique S/634/2007 Annex 1 page 4 Annex 1 LIST OF APPROVED DATA RECOMMENDED FOR INCLUSION IN THE OPCW CENTRAL ANALYTICAL DATABASE Note: In the last column of the tables that follow in this and the next Annex, “A” means “accepted”; “B”, “accepted subject to minor corrections”. A “1” under the “Column” heading means an HP5 or an SE54 column. TABLE 1. LIST OF APPROVED MS DATA OPCW Chemical Name Schedule Decision Code 04-2-0374r Diisopropyl methylphosphonate 2.B.04 A 04-2-0450 Nonyl S-2-diethylaminoethyl ethylphosphonothiolate 1.A.03 A 04-2-0452 Decyl S-2-diethylaminoethyl ethylphosphonothiolate 1.A.03 A 04-2-0453 1-Methylnonyl S-2-diethylaminoethyl ethylphosphonothiolate 1.A.03 A 04-2-0454 Cyclopentyl S-2-diethylaminoethyl ethylphosphonothiolate 1.A.03 A 04-2-0455 Cyclohexyl S-2-diethylaminoethyl ethylphosphonothiolate 1.A.03 A 04-2-0456 Cycloheptyl S-2-diethylaminoethyl ethylphosphonothiolate 1.A.03 A 04-2-0457 2-Methylcyclohexyl S-2-diethylaminoethyl 1.A.03 A ethylphosphonothiolate 04-2-0458 Cyclooctyl S-2-diethylaminoethyl ethylphosphonothiolate 1.A.03 A 04-2-0459 tert-Butyl S-2-diethylaminoethyl ethylphosphonothiolate 1.A.03 A 04-2-0460 3-Methylbutyl S-2-diethylaminoethyl ethylphosphonothiolate 1.A.03 A 04-2-0461 1,1-Dimethylpropyl S-2-diethylaminoethyl 1.A.03 A ethylphosphonothiolate 08-2-0117 O-Cyclopentyl S-ethyl methylphosphonothiolate 2.B.04 A 09-2-0013r Butyl N,N-diethylphosphoramidocyanidate 1.A.02 A 09-2-0015r Cyclohexyl N,N-diethylphosphoramidocyanidate 1.A.02 A 09-2-0023r Cyclohexyl N,N-dipropylphosphoramidocyanidate 1.A.02 A 09-2-0024r 2-Ethylhexyl N,N-dipropylphosphoramidocyanidate 1.A.02 A 09-2-0028r Propyl N-ethyl-N-methylphosphoramidocyanidate 1.A.02 A 09-2-0029r sec-Butyl N-ethyl-N-methylphosphoramidocyanidate 1.A.02 A 09-2-0038r Methyl N-methyl-N-propylphosphoramidocyanidate 1.A.02 A 09-2-0039r Ethyl N-methyl-N-propylphosphoramidocyanidate 1.A.02 A 09-2-0040r Propyl N-methyl-N-propylphosphoramidocyanidate 1.A.02 A 09-2-0041r Butyl N-methyl-N-propylphosphoramidocyanidate 1.A.02 A 09-2-0042r Pentyl N-methyl-N-propylphosphoramidocyanidate 1.A.02 A 09-2-0043r Hexyl N-methyl-N-propylphosphoramidocyanidate 1.A.02 A 09-2-0044r Isopropyl N-methyl-N-propylphosphoramidocyanidate 1.A.02 A 09-2-0045r Isobutyl N-methyl-N-propylphosphoramidocyanidate 1.A.02 A 09-2-0046r 1-Ethylpropyl N-methyl-N-propylphosphoramidocyanidate 1.A.02 A 09-2-0047r 3-Methylbutyl N-methyl-N-propylphosphoramidocyanidate 1.A.02 A 09-2-0048r Cyclohexyl N-methyl-N-propylphosphoramidocyanidate 1.A.02 A 09-2-0049r sec-Butyl N-methyl-N-propylphosphoramidocyanidate 1.A.02 A 09-2-0051r Octyl N-methyl-N-propylphosphoramidocyanidate 1.A.02 A 09-2-0061r 3-Methylbutyl N-isopropyl-N-methylphosphoramidocyanidate 1.A.02 A 09-2-0064r Hexyl N-isopropyl-N-methylphosphoramidocyanidate 1.A.02 A 09-2-0066r Octyl N-isopropyl-N-methylphosphoramidocyanidate 1.A.02 A 09-2-0074r 3-Methylbutyl N-ethyl-N-propylphosphoramidocyanidate 1.A.02 A 09-2-0075r Hexyl N-ethyl-N-propylphosphoramidocyanidate 1.A.02 A S/634/2007 Annex 1 page 5 OPCW Chemical Name Schedule Decision Code 09-2-0079r Isopropyl N-ethyl-N-propylphosphoramidocyanidate 1.A.02 A 09-2-0080r 1-Ethylpropyl N-ethyl-N-propylphosphoramidocyanidate 1.A.02 A 09-2-0081r Octyl N-ethyl-N-propylphosphoramidocyanidate 1.A.02 A 09-2-0086r Pentyl N-ethyl-N-isopropylphosphoramidocyanidate 1.A.02 A 09-2-0089r Isobutyl N-ethyl-N-isopropylphosphoramidocyanidate 1.A.02 A 09-2-0090r 1-Ethylpropyl N-ethyl-N-isopropylphosphoramidocyanidate 1.A.02 A 09-2-0092r Octyl N-ethyl-N-isopropylphosphoramidocyanidate 1.A.02 A 09-2-0094r Hexyl N-ethyl-N-isopropylphosphoramidocyanidate 1.A.02 A 09-2-0099r Butyl N-isopropyl-N-propylphosphoramidocyanidate 1.A.02 A 14-2-0024 Octyl methylphosphonochloridate 2.B.04 B 14-2-0025 1-Methylheptyl methylphosphonochloridate 2.B.04 B 14-2-0026 1-Ethylpropyl ethylphosphonochloridate 2.B.04 B 14-2-0027 3-Methylbutyl ethylphosphonochloridate 2.B.04 B 14-2-0028 1,2-Dimethylbutyl ethylphosphonochloridate 2.B.04 B 14-2-0029 Cyclohexyl isopropylphosphonochloridate 2.B.04 B 14-2-0030 4,4-Dimethylcyclohexyl methylphosphonofluoridate 1.A.01 B 14-2-0031 Cyclopropylmethyl isopropylphosphonofluoridate 1.A.01 B 14-2-0033 2-Dipropylaminoethyl methylphosphonofluoridate 2.B.04 B 14-2-0034 2-Diisopropylaminoethyl methylphosphonofluoridate 2.B.04 B 14-2-0036
Recommended publications
  • Regulated Substance List
    INSTRUCTIONS FOR THE UNIFIED PROGRAM (UP) FORM REGULATED SUBSTANCE LIST CHEMICAL NAME CAS # TQ Listing CHEMICAL NAME CAS # TQ Listing (Lbs) Basis (Lbs) Basis Acetaldehyde 75-07-0 10,000 g Cantharidin 56-25-7 100/10,0001 * Acetone Cyanohydrin 75-86-5 1,000 Carbachol Chloride 51-83-2 500/10,0001 Acetone Thiosemicarbazide 1752-30-3 1,000/10,0001 Acetylene (Ethyne) 74-86-2 10,000 f Carbamic Acid, Methyl-,o- Acrolein (2-Propenal) 107-02-8 500 b (((2,4-Dimethyl-1,3-Dithiolan- Acrylamide 79-06-1 1,000/10,0001 2-YL) Methylene)Amino)- 26419-73-8 100/10,0001 Acrylonitrile (2- Propenenitrile) 107-13-1 10,000 b Carbofuran 1563-66-2 10/10,0001 Acrylyl Chloride Carbon Disulfide 75-15-0 10,000 b (2-Propenoyl Chloride) 814-68-6 100 b Carbon Oxysulfide Aldicarb 116-06-3 100/10,0001 (Carbon Oxide Sulfide (COS)) 463-58-1 10,000 f Aldrin 309-00-2 500/10,0001 Chlorine 7782-50-5 100 a,b Allyl Alcohol (2-Propen-1-ol) 107-18-6 1,000 b Chlorine Dioxide Allylamine (2-Propen-1-Amine) 107-11-9 500 b (Chlorine Oxide (ClO2)) 10049-04-4 1,000 c Aluminum Phosphide 20859-73-8 500 Chlorine Monoxide (Chlorine Oxide) 7791-21-1 10,000 f Aminopterin 54-62-6 500/10,0001 Chlormequat Chloride 999-81-5 100/10,0001 Amiton Oxalate 3734-97-2 100/10,0001 Chloroacetic Acid 79-11-8 100/10,0001 Ammonia, Anhydrous 2 7664-41-7 500 a,b Chloroform 67-66-3 10,000 b Ammonia, Aqueous Chloromethyl Ether (conc 20% or greater) 7664-41-7 20,000 a,b (Methane,Oxybis(chloro-) 542-88-1 100 b * Aniline 62-53-3 1,000 Chloromethyl Methyl Ether Antimycin A 1397-94-0 1,000/10,0001 (Chloromethoxymethane)
    [Show full text]
  • The Detection and Determination of Esters
    Louisiana State University LSU Digital Commons LSU Historical Dissertations and Theses Graduate School 1958 The etD ection and Determination of Esters. Mohd. Mohsin Qureshi Louisiana State University and Agricultural & Mechanical College Follow this and additional works at: https://digitalcommons.lsu.edu/gradschool_disstheses Recommended Citation Qureshi, Mohd. Mohsin, "The eD tection and Determination of Esters." (1958). LSU Historical Dissertations and Theses. 501. https://digitalcommons.lsu.edu/gradschool_disstheses/501 This Dissertation is brought to you for free and open access by the Graduate School at LSU Digital Commons. It has been accepted for inclusion in LSU Historical Dissertations and Theses by an authorized administrator of LSU Digital Commons. For more information, please contact [email protected]. Copright by Mohcl Mohsin Qureshi 1959 THE DETECTION AND DETERMINATION OF ESTERS A Dissertation Submitted to the Graduate Faculty of the Louisiana State University and Agricultural and Mechanical College in partial fulfillment of the requirements for the degree of Doctor of Philosophy in The Department of Chemistry by Mohd. Mohsin Qureshi M.Sc., Aligarh University, 1944 August, 1958 ACKNOWLEDGMENT The author wishes to express his sincere apprecia­ tion and gratitude to Dr. Philip W. West under whose guidance this research was carried out. He is grateful to Dr. James G. Traynham for sup­ plying him with a number of esters and for his many helpful suggestions. The financial support given to him by the Continental Oil Company is gratefully acknowledged. He offers his sincere thanks to Miss Magdalena Usategul for her valuable suggestions and her ungrudging help during the course of this investigation. Dr. Anil K.
    [Show full text]
  • Aldrich Vapor
    Aldrich Vapor Library Listing – 6,611 spectra This library is an ideal tool for investigator using FT-IR to analyze gas phase materials. It contains gas phase spectra collected by Aldrich using a GC-IR interface to ensure chromatographically pure samples. The Aldrich FT-IR Vapor Phase Library contains 6,611 gas phase FT-IR spectra collected by Aldrich Chemical Company using a GC interface. The library includes compound name, molecular formula, CAS (Chemical Abstract Service) registry number, Aldrich catalog number, and page number in the Aldrich Library of FT-IR Spectra, Edition 1, Volume 3, Vapor-Phase. Aldrich Vapor Index Compound Name Index Compound Name 6417 ((1- 3495 (1,2-Dibromoethyl)benzene; Styrene Ethoxycyclopropyl)oxy)trimethylsilane dibromide 2081 (+)-3-(Heptafluorobutyryl)camphor 3494 (1-Bromoethyl)benzene; 1-Phenylethyl 2080 (+)-3-(Trifluoroacetyl)camphor bromide 262 (+)-Camphene; 2,2-Dimethyl-3- 6410 (1-Hydroxyallyl)trimethylsilane methylenebicyclo[2.2.1]heptane 6605 (1-Methyl-2,4-cyclopentadien-1- 2828 (+)-Diisopropyl L-tartrate yl)manganese tricarbonyl 947 (+)-Isomenthol; [1S-(1a,2b,5b)]-2- 6250 (1-Propynyl)benzene; 1-Phenylpropyne Isopropyl-5-methylcyclohexano 2079 (1R)-(+)-3-Bromocamphor, endo- 1230 (+)-Limonene oxide, cis + trans; (+)-1,2- 2077 (1R)-(+)-Camphor; (1R)-(+)-1,7,7- Epoxy-4-isopropenyl-1- Trimethylbicyclo[2.2.1]heptan- 317 (+)-Longifolene; (1S)-8-Methylene- 976 (1R)-(+)-Fenchyl alcohol, endo- 3,3,7-trimethyltricyclo[5.4.0 2074 (1R)-(+)-Nopinone; (1R)-(+)-6,6- 949 (+)-Menthol; [1S-(1a,2b,5a)]-(+)-2- Dimethylbicyclo[3.1.1]heptan-2-
    [Show full text]
  • Warfare Agents for Modeling Airborne Dispersion in and Around Buildings
    LBNL-45475 ERNEST ORLANDO LAWRENCE BERKELEY NATIn NAL LABORATORY Databaseof Physical,Chemicaland ToxicologicalPropertiesof Chemical and Biological(CB)WarfitreAgentsfor ModelingAirborneDispersionIn and AroundBuildings TracyThatcher,RichSextro,andDonErmak Environmental Energy Technologies Division DISCLAIMER This document was prepared as an account of work sponsored by the United States Government. While this document is believed to contain correct information, neither the United States Government nor any agency thereof, nor The Regents of the University of Catifomia, nor any of their employees, makes any warranty, express or implied, or assumes any legal responsibility for the accuracy, completeness, or usefulness of anY information, apparatus, product, or process disclosed, or represents that its use would not infringe privately owned rights. Reference herein to any specific commercial product, process, or service by its trade name, trademark, manufacturer, or otherwise, does not necessarily constitute or imply its endorsement, recommend at i on, or favoring by the United States Government or any agency thereof, or The Regents of the University of California. The views and opinions of authors expressed herein do not necessarily state or reflect those of the United States Government or any agency thereof, or The Regents of the University of California. Ernest Orlando Lawrence Berkeley National Laboratory is an equal opportunity employer. DISCLAIMER Portions of this document may be illegible in electronic image products. Images are produced
    [Show full text]
  • Aldrich Raman
    Aldrich Raman Library Listing – 14,033 spectra This library represents the most comprehensive collection of FT-Raman spectral references available. It contains many common chemicals found in the Aldrich Handbook of Fine Chemicals. To create the Aldrich Raman Condensed Phase Library, 14,033 compounds found in the Aldrich Collection of FT-IR Spectra Edition II Library were excited with an Nd:YVO4 laser (1064 nm) using laser powers between 400 - 600 mW, measured at the sample. A Thermo FT-Raman spectrometer (with a Ge detector) was used to collect the Raman spectra. The spectra were saved in Raman Shift format. Aldrich Raman Index Compound Name Index Compound Name 4803 ((1R)-(ENDO,ANTI))-(+)-3- 4246 (+)-3-ISOPROPYL-7A- BROMOCAMPHOR-8- SULFONIC METHYLTETRAHYDRO- ACID, AMMONIUM SALT PYRROLO(2,1-B)OXAZOL-5(6H)- 2207 ((1R)-ENDO)-(+)-3- ONE, BROMOCAMPHOR, 98% 12568 (+)-4-CHOLESTEN-3-ONE, 98% 4804 ((1S)-(ENDO,ANTI))-(-)-3- 3774 (+)-5,6-O-CYCLOHEXYLIDENE-L- BROMOCAMPHOR-8- SULFONIC ASCORBIC ACID, 98% ACID, AMMONIUM SALT 11632 (+)-5-BROMO-2'-DEOXYURIDINE, 2208 ((1S)-ENDO)-(-)-3- 97% BROMOCAMPHOR, 98% 11634 (+)-5-FLUORODEOXYURIDINE, 769 ((1S)-ENDO)-(-)-BORNEOL, 99% 98+% 13454 ((2S,3S)-(+)- 11633 (+)-5-IODO-2'-DEOXYURIDINE, 98% BIS(DIPHENYLPHOSPHINO)- 4228 (+)-6-AMINOPENICILLANIC ACID, BUTANE)(N3-ALLYL)PD(II) CL04, 96% 97 8167 (+)-6-METHOXY-ALPHA-METHYL- 10297 ((3- 2- NAPHTHALENEACETIC ACID, DIMETHYLAMINO)PROPYL)TRIPH 98% ENYL- PHOSPHONIUM BROMIDE, 12586 (+)-ANDROSTA-1,4-DIENE-3,17- 99% DIONE, 98% 13458 ((R)-(+)-2,2'- 963 (+)-ARABINOGALACTAN BIS(DIPHENYLPHOSPHINO)-1,1'-
    [Show full text]
  • Scientific Advisory Board
    OPCW Scientific Advisory Board Eleventh Session SAB-11/1 11 – 13 February 2008 13 February 2008 Original: ENGLISH REPORT OF THE ELEVENTH SESSION OF THE SCIENTIFIC ADVISORY BOARD 1. AGENDA ITEM ONE – Opening of the Session The Scientific Advisory Board (SAB) met for its Eleventh Session from 11 to 13 February 2008 at the OPCW headquarters in The Hague, the Netherlands. The Session was opened by the Vice-Chairperson of the SAB, Mahdi Balali-Mood. The meeting was chaired by Philip Coleman of South Africa, and Mahdi Balali-Mood of the Islamic Republic of Iran served as Vice-Chairperson. A list of participants appears as Annex 1 to this report. 2. AGENDA ITEM TWO – Adoption of the agenda 2.1 The SAB adopted the following agenda for its Eleventh Session: 1. Opening of the Session 2. Adoption of the agenda 3. Tour de table to introduce new SAB Members 4. Election of the Chairperson and the Vice-Chairperson of the SAB1 5. Welcome address by the Director-General 6. Overview on developments at the OPCW since the last session of the SAB 7. Establishment of a drafting committee 8. Work of the temporary working groups: (a) Consideration of the report of the second meeting of the sampling-and-analysis temporary working group; 1 In accordance with paragraph 1.1 of the rules of procedure for the SAB and the temporary working groups of scientific experts (EC-XIII/DG.2, dated 20 October 1998) CS-2008-5438(E) distributed 28/02/2008 *CS-2008-5438.E* SAB-11/1 page 2 (b) Status report by the Industry Verification Branch on the implementation of sampling and analysis for Article VI inspections; (c) Presentation by the OPCW Laboratory; (d) Update on education and outreach; and (e) Update on the formation of the temporary working group on advances in science and technology and their potential impact on the implementation of the Convention: (i) composition of the group; and (ii) its terms of reference 9.
    [Show full text]
  • Pacs by Chemical Name (Mg/M3) (Pdf)
    Table 4: Protective Action Criteria (PAC) Rev 25 based on applicable 60-minute AEGLs, ERPGs, or TEELs. Values are presented in mg/m3. August 2009 Table 4 is an alphabetical listing of the chemicals in the PAC data set. It provides Chemical Abstract Service Registry Numbers (CASRNs)1, PAC values, and technical information on the source of the PAC values. Table 4 presents all values for TEEL-0, PAC-1, PAC-2, and PAC-3 in mg/m3. The conversion of ppm to mg/m3 is calculated assuming 25 ºC and 760 mm Hg. The columns presented in Table 4 provide the following information: Heading Definition No. The ordered numbering of the chemicals as they appear in this alphabetical listing. Chemical Name The chemical name given to the PAC Development Team. CASRN The Chemical Abstract Service Registry Number for this chemical. TEEL-0 This is the threshold concentration below which most people will experience no adverse health effects. This PAC is always based on TEEL-0 because AEGL-0 or ERPG-0 values do not exist. PAC-1 Based on the applicable AEGL-1, ERPG-1, or TEEL-1 value. PAC-2 Based on the applicable AEGL-2, ERPG-2, or TEEL-2 value. PAC-3 Based on the applicable AEGL-3, ERPG-3, or TEEL-3 value. Source of PACs: Technical comments provided by the PAC development team that TEEL-0, PAC-1, indicate the source of the data used to derive PAC values. Future efforts PAC-2, PAC-3 are directed at reviewing, revising, and enhancing this information.
    [Show full text]
  • WO 2016/147132 Al 22 September 2016 (22.09.2016) P O P C T
    (12) INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property Organization International Bureau (10) International Publication Number (43) International Publication Date WO 2016/147132 Al 22 September 2016 (22.09.2016) P O P C T (51) International Patent Classification: (81) Designated States (unless otherwise indicated, for every C07C 227/32 (2006.01) C07D 405/04 (2006.01) kind of national protection available): AE, AG, AL, AM, AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, (21) International Application Number: BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DK, DM, PCT/IB20 16/05 14 1 DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, (22) International Filing Date: HN, HR, HU, ID, IL, IN, IR, IS, JP, KE, KG, KN, KP, KR, 17 March 2016 (17.03.2016) KZ, LA, LC, LK, LR, LS, LU, LY, MA, MD, ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, OM, (25) Filing Language: English PA, PE, PG, PH, PL, PT, QA, RO, RS, RU, RW, SA, SC, (26) Publication Language: English SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW. (30) Priority Data: 895/MUM/2015 18 March 2015 (18.03.2015) (84) Designated States (unless otherwise indicated, for every kind of regional protection available): ARIPO (BW, GH, (71) Applicant: PIRAMAL ENTERPRISES LIMITED GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, ST, SZ, [IN/IN]; Piramal Tower, Ganpatrao Kadam Marg, Lower TZ, UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, RU, Parel, Mumbai 400 013 (IN).
    [Show full text]
  • The Use of Natural Product Substrates for the Synthesis of Libraries of Biologically Active, New Chemical Entities
    University of Montana ScholarWorks at University of Montana Graduate Student Theses, Dissertations, & Graduate School Professional Papers 2010 The seU of Natural Product Substrates for the Synthesis of Libraries of Biologically Active, New Chemical Entities Joshua Bryant Phillips The University of Montana Let us know how access to this document benefits ouy . Follow this and additional works at: https://scholarworks.umt.edu/etd Recommended Citation Phillips, Joshua Bryant, "The sU e of Natural Product Substrates for the Synthesis of Libraries of Biologically Active, New Chemical Entities" (2010). Graduate Student Theses, Dissertations, & Professional Papers. 1100. https://scholarworks.umt.edu/etd/1100 This Dissertation is brought to you for free and open access by the Graduate School at ScholarWorks at University of Montana. It has been accepted for inclusion in Graduate Student Theses, Dissertations, & Professional Papers by an authorized administrator of ScholarWorks at University of Montana. For more information, please contact [email protected]. THE USE OF NATURAL PRODUCT SUBSTRATES FOR THE SYNTHESIS OF LIBRARIES OF BIOLOGICALLY ACTIVE, NEW CHEMICAL ENTITIES by Joshua Bryant Phillips B.S. Chemistry, Northern Arizona University, 2002 B.S. Microbiology (health pre-professional), Northern Arizona University, 2002 Presented in partial fulfillment of the requirements for the degree of Doctor of Philosophy Chemistry The University of Montana June 2010 Phillips, Joshua Bryant Ph.D., June 2010 Chemistry THE USE OF NATURAL PRODUCT SUBSTRATES FOR THE SYNTHESIS OF LIBRARIES OF BIOLOGICALLY ACTIVE, NEW CHEMICAL ENTITIES Advisor: Dr. Nigel D. Priestley Chairperson: Dr. Bruce Bowler ABSTRACT Since Alexander Fleming first noted the killing of a bacterial culture by a mold, antibiotics have revolutionized medicine, being able to treat, and often cure life-threatening illnesses and making surgical procedures possible by eliminating the possibility of opportunistic infection.
    [Show full text]
  • ITAR Category
    Category XIV—Toxicological Agents, Including Chemical Agents, Biological Agents, and Associated Equipment *(a) Chemical agents, to include: (1) Nerve agents: (i) O-Alkyl (equal to or less than C10, including cycloalkyl) alkyl (Methyl, Ethyl, n-Propyl or Isopropyl)phosphonofluoridates, such as: Sarin (GB): O-Isopropyl methylphosphonofluoridate (CAS 107–44–8) (CWC Schedule 1A); and Soman (GD): O-Pinacolyl methylphosphonofluoridate (CAS 96–64–0) (CWC Schedule 1A); (ii) O-Alkyl (equal to or less than C10, including cycloalkyl) N,N-dialkyl (Methyl, Ethyl, n- Propyl or Isopropyl)phosphoramidocyanidates, such as: Tabun (GA): O-Ethyl N, N- dimethylphosphoramidocyanidate (CAS 77–81–6) (CWC Schedule 1A); (iii) O-Alkyl (H or equal to or less than C10, including cycloalkyl) S–2-dialkyl (Methyl, Ethyl, n- Propyl or Isopropyl)aminoethyl alkyl (Methyl, Ethyl, n-Propyl or Isopropyl)phosphonothiolates and corresponding alkylated and protonated salts, such as: VX: O-Ethyl S-2- diisopropylaminoethyl methyl phosphonothiolate (CAS 50782–69–9) (CWC Schedule 1A); (2) Amiton: O,O-Diethyl S-[2(diethylamino)ethyl] phosphorothiolate and corresponding alkylated or protonated salts (CAS 78–53–5) (CWC Schedule 2A); (3) Vesicant agents: (i) Sulfur mustards, such as: 2-Chloroethylchloromethylsulfide (CAS 2625–76–5) (CWC Schedule 1A); Bis(2-chloroethyl)sulfide (CAS 505–60–2) (CWC Schedule 1A); Bis(2- chloroethylthio)methane (CAS 63839–13–6) (CWC Schedule 1A); 1,2-bis (2- chloroethylthio)ethane (CAS 3563–36–8) (CWC Schedule 1A); 1,3-bis (2-chloroethylthio)-n- propane (CAS
    [Show full text]
  • Investigation and Risk Assessment of Ships Loaded with Chemical Ammunition Scuttled in Skagerrak
    Investigation and risk assessment of ships loaded with chemical ammunition scuttled in Skagerrak TA-1907/2002 Tørnes John Aa, Voie Øyvind A, Ljønes Marita, Opstad Aase M, Bjerkeseth Leif Haldor, Hussain Fatima Investigation and risk assessment of ships loaded with chemical ammunition scuttled in Skagerrak (TA-1907/2002) Preface The current report gives a description of the investigation carried out by Forsvarets forskningsinstitutt (FFI) of the wrecks dumped in Skagerrak after World War II with chemical ammunition on board. The aim of the investigation was to give an evaluation of the conditions of the dumped wrecks and to assess whether the chemical warfare agents have leaked out from the wrecks. This was done by using a remote-operated vehicle with video cameras. Sediment samples were collected and analysed with respect to chemical warfare agents and some related compounds. Temperature and sea current at the sea bottom was measured. This made it possible to give a rough estimate of the risks associated with leaking ammunition. Some recommendation for further work is also given. FFI, Kjeller, November 2002 Bjørn A Johnsen Director of Research 3 Investigation and risk assessment of ships loaded with chemical ammunition scuttled in Skagerrak (TA-1907/2002) 4 Investigation and risk assessment of ships loaded with chemical ammunition scuttled in Skagerrak (TA-1907/2002) Contents 1. Summary..................................................................................................7 1.1 Background .................................................................................................................
    [Show full text]
  • Justin Pals.Pdf
    MECHANISMS OF MONOHALOGENATED ACETIC ACID INDUCED GENOMIC DNA DAMAGE BY JUSTIN A. PALS DISSERTATION Submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy in Crop Sciences in the Graduate College of the University of Illinois at Urbana-Champaign, 2014 Urbana, Illinois Doctoral Committee: Professor Michael J. Plewa, Chair Professor Benito J. Mariñas Professor A. Layne Rayburn Brian K. Miller, Director of Illinois-Indiana Sea Grant ABSTRACT Disinfection of drinking water stands among the greatest public health achievements in human history. Killing or inactivation of pathogenic microbes by chemical oxidants such as chlorine, chloramine, or ozone have greatly reduced incidence of waterborne diseases. However, the disinfectant also reacts with organic and inorganic matter in the source water and generates a mixture of toxic disinfection byproducts (DBPs) as an unintended consequence. Since they were first discovered in 1974, over 600 individual DBPs have been detected in disinfected water. Exposure to DBPs is associated with increased risks for developing cancers of the colon, rectum, and bladder, and also for adverse pregnancy outcomes including small for gestational age and congenital malformations. While individual DBPs are teratogenic or carcinogenic, because they are formed at low concentrations during disinfection, it is unlikely that any one DBP can account for these increased risks. While genotoxicity and oxidative stress have been suggested, the mechanisms connecting DBP exposures to adverse health and pregnancy outcomes remain unknown. Investigating mechanisms of toxicity for individual, or classes of DBPs will provide a better understanding of how multiple DBPs interact to generate adverse health and pregnancy outcomes. Monohalogenated acetic acids (monoHAAs) iodoacetic acid (IAA), bromoacetic acid (BAA), and chloroacetic acid (CAA) are genotoxic and mutagenic with the consistent rank order of toxicity of IAA > BAA > CAA.
    [Show full text]