Acutely Toxic Chemicals Chemical Class Standard Operating Procedure
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Quinolines from the Cyclocondensation of Isatoic Anhydride with Ethyl Acetoacetate: Preparation of Ethyl 4- Hydroxy-2-Methylquinoline-3-Carboxylate and Derivatives
Supporting Information for Quinolines from the cyclocondensation of isatoic anhydride with ethyl acetoacetate: preparation of ethyl 4- hydroxy-2-methylquinoline-3-carboxylate and derivatives Nicholas G. Jentsch, Jared D. Hume, Emily B. Crull, Samer M. Beauti, Amy H. Pham, Julie A. Pigza, Jacques J. Kessl and Matthew G. Donahue* Address: 1Department of Chemistry and Biochemistry, University of Southern Mississippi, 118 College Drive #5043, Hattiesburg, MS 39406 Email: Matthew G. Donahue - [email protected] *Corresponding author Experimental procedures and analytical data Table of contents General Procedures .......................................................................................................... S3 1H-Benzo[d][1,3]oxazine-2,4-dione (9a): ........................................................................... S7 6-Bromo-1H-benzo[d][1,3]oxazine-2,4-dione (9b): ............................................................ S8 6-Iodo-1H-benzo[d][1,3]oxazine-2,4-dione (9c): ................................................................ S8 6-Hydroxy-1H-benzo[d][1,3]oxazine-2,4-dione (9d): ......................................................... S9 6-Nitro-1H-benzo[d][1,3]oxazine-2,4-dione(9e): ................................................................ S9 7-Bromo-1H-benzo[d][1,3]oxazine-2,4-dione (9f): ............................................................. S9 S1 7-Nitro-1H-benzo[d][1,3]oxazine-2,4-dione (9g): ............................................................... S10 8-Bromo-1H-benzo[d][1,3]oxazine-2,4-dione -
Carbonylation of Protected Or Non-Protected 2-Bromobenzaldehyde Catalyzed by Cobalt Carbonyl
772 Bull. Korean Chem. Soc. 1994, Vol. 15, No. 9 Sang Chui Shim et al. Carbonylation of Protected or Non-protected 2-Bromobenzaldehyde Catalyzed by Cobalt Carbonyl Sang Chui S버 m*, Dong Yub Lee, Heung Jin Choi, Chil Hoon Doh1, and Keun Tai Huh* ^Department of Industrial Chemistry, Kyungpook National University, Taegu 701-702, Korea ^Department of Materials Science and Engineering Kyungsung University, Pusan 608-736, Korea Korea Electrotechnology Research Institute, Changwon, Korea Received May 11, 1994 The cobalt catalyzed carbonylation of bromobenzene having protected aldehyde group gives the corresponding ester in good yields, but 2-bromobenzaldehyde gives 3-alkoxyphthalide in the noticeable yield instead of alkyl 2-formylben- zoates. Introduction Table 1. Carbonylation of 2-Bromobenzenes Having Protected Aldehyde Groups to 2-Substituted Alkyl Benzoates Catalyzed by The metal-catalyzed carbonyl가 ion of aryl halides has ver Cobalt CarbonyF satile utility in the preparative organic chemistry1. Of many Run Reactant catalysts2 used in the carbonylation of aryl halides cobalt Alcohol Product Yield (%y carbonyl species have been conducted under mild conditions, 1 1 CH3CH2OH 2b 88 room temperature and one atmospheric pressure of carbon 2 1 CH3CH2OH 2b 75 。 monoxide. More recently, using dicobalt octacarbonyl at room 3 1 CH3CH2OH 2b 38d temperature under one atmospheric pressure of carbon mo 4 1 CH3OH 2a 80 noxide many applications were reported on the carbonylation 5 1 CH3CH2CH2OH 2c 85 of benzal halides,3-5 and halo (halomethyl)benzenes6-8. 6 (CH3)2CHOH 21 However, studies2,9-11 on the carbonylation of aryl halides 1 2d 7 CH3CH2CH2CH2OH having other reactive functional groups are rare. -
Supporting Information Lewis Acid–Base Synergistic Catalysis Of
Electronic Supplementary Material (ESI) for ChemComm. This journal is © The Royal Society of Chemistry 2020 Supporting information Lewis acid–base synergistic catalysis of cationic halogen-bonding-donors with nucleophilic counter anions Koki Torita,a Ryosuke Haraguchi,*b Yoshitsugu Morita,a Satoshi Kemmochi,a Teruyuki Komatsu,a and Shin-ichi Fukuzawa*a aDepartment of Applied Chemistry, Institute of Science and Engineering, Chuo University, 1-13-27 Kasuga, Bunkyo-ku, 112-8551 Tokyo, Japan bDepartment of Applied Chemistry, Faculty of Engineering, Chiba Institute of Technology, 2-17-1 Tsudanuma, Narashino, Chiba 275-0016, Japan. Contents Instrumentation and Chemicals S2 Effect of Counter Anions on the Catalytic Activity S4 Effect of Water on the Catalytic Efficiency S4 NMR Titration Experiment S5 Experimental Procedure S7 Characterization Data S11 Theoretical Study S18 NMR Spectra Data S38 References S77 S1 Instrumentation and Chemicals All manipulations of oxygen- and moisture-sensitive materials were conducted under argon or nitrogen atmosphere in a flame dried Schlenk flask. Nuclear magnetic resonance spectra were taken on a JEOL ECA spectrometer using tetramethylsilane for 1 H NMR as an internal standard (δ = 0 ppm) when CDCl3 was used as a solvent, using 1 CD3CN for H NMR as an internal standard (δ = 1.94 ppm) when CD3CN was used as a 1 solvent, using (CD3)2SO for H NMR as an internal standard (δ = 2.50 ppm) when 13 (CD3)2SO was used as a solvent, using CDCl3 for C NMR as an internal standard (δ = 13 77.16 ppm) when CDCl3 was used as a solvent, using CD3CN for C NMR as an internal standard (δ = 118.26 ppm) when CD3CN was used as a solvent, using (CD3)2SO 13 for C NMR as an internal standard (δ = 39.52 ppm) when (CD3)2SO was used as a solvent. -
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. -
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- -
Transfer of Bromoform Present in Asparagopsis Taxiformis to Milk and Urine of Lactating Dairy Cows
foods Article Safety and Transfer Study: Transfer of Bromoform Present in Asparagopsis taxiformis to Milk and Urine of Lactating Dairy Cows Wouter Muizelaar 1,2,* , Maria Groot 3 , Gert van Duinkerken 1, Ruud Peters 3 and Jan Dijkstra 2 1 Wageningen Livestock Research, Wageningen University & Research, P.O. Box 338, 6700 AH Wageningen, The Netherlands; [email protected] 2 Animal Nutrition Group, Wageningen University & Research, P.O. Box 338, 6700 AH Wageningen, The Netherlands; [email protected] 3 Wageningen Food Safety Research, Wageningen University & Research, P.O. Box 230, 6700 AE Wageningen, The Netherlands; [email protected] (M.G.); [email protected] (R.P.) * Correspondence: [email protected]; Tel.: +31-317-487-941 Abstract: Enteric methane (CH4) is the main source of greenhouse gas emissions from ruminants. The red seaweeds Asparagopsis taxiformis (AT) and Asparagopsis armata contain halogenated compounds, including bromoform (CHBr3), which may strongly decrease enteric CH4 emissions. Bromoform is known to have several toxicological effects in rats and mice and is quickly excreted by the animals. This study investigated the transfer of CHBr3 present in AT to milk, urine, feces, and animal tissue when incorporated in the diet of dairy cows. Twelve lactating Holstein-Friesian dairy cows were randomly assigned to three treatment groups, representing the target dose (low), 2× target dose (medium), and 5× target dose (high). The adaptation period lasted seven days, and subsequently Citation: Muizelaar, W.; Groot, M.; cows were fed AT for 22 days maximally. The transfer of CHBr3 to the urine at days 1 and 10 (10–148 van Duinkerken, G.; Peters, R.; µg/L) was found with all treatments. -
MATERIAL SAFETY DATA SHEET According to the Hazard Communication Standard (29 CFR 1910.1200)
MATERIAL SAFETY DATA SHEET according to the Hazard Communication Standard (29 CFR 1910.1200) Date of issue: 12/20/2012 Version 1.0 SECTION 1. Identification Product identifier Product number 101944 Product name Bromoform for separation of minerals mixtures Relevant identified uses of the substance or mixture and uses advised against Identified uses Reagent for analysis Details of the supplier of the safety data sheet Company EMD Millipore Corporation | 290 Concord Road, Billerica, MA 01821, United States of America | SDS Phone Support: +1-978-715-1335 | General Inquiries: +1-978-751-4321 | Monday to Friday, 9:00 AM to 4:00 PM Eastern Time (GMT-5) e-mail: [email protected] Emergency telephone 800-424-9300 CHEMTREC (USA) +1-703-527-3887 CHEMTREC (International) 24 Hours/day; 7 Days/week SECTION 2. Hazards identification GHS Classification Acute toxicity, Category 3, Inhalation, H331 Acute toxicity, Category 4, Oral, H302 Eye irritation, Category 2, H319 Skin irritation, Category 2, H315 Chronic aquatic toxicity, Category 2, H411 For the full text of the H-Statements mentioned in this Section, see Section 16. GHS-Labeling Hazard pictograms Signal Word Danger Hazard Statements H331 Toxic if inhaled. Page 1 of 11 MATERIAL SAFETY DATA SHEET according to the Hazard Communication Standard (29 CFR 1910.1200) Product number 101944 Version 1.0 Product name Bromoform for separation of minerals mixtures H302 Harmful if swallowed. H319 Causes serious eye irritation. H315 Causes skin irritation. H411 Toxic to aquatic life with long lasting effects. Precautionary Statements P273 Avoid release to the environment. P304 + P340 IF INHALED: Remove victim to fresh air and keep at rest in a position comfortable for breathing. -
Ionic Compound Ratios Time: 1 -2 Class Periods
Collisions Lesson Plan Ionic Compound Ratios Time: 1 -2 class periods Lesson Description In this lesson, students will use Collisions to explore the formation of ionic compounds and compound ratios. Key Essential Questions 1. What makes up an ionic compound? 2. Are ionic compounds found in common ratios? Learning Outcomes Students will be able to determine the ionic compound ratio of an ionic compound. Prior Student Knowledge Expected Cations are postiviely charged ions and anions are negatively charged ions. Lesson Materials • Individual student access to Collisions on tablet, Chromebook, or computer. • Projector / display of teacher screen • Accompanying student resources (attached) Standards Alignment NGSS Alignment Science & Enginnering Practices Disciplinary Core Ideas Crosscutting Concepts • Developing and using • HS-PS-12. Construct and • Structure and Function models revise an explanation for the • Construcing explanations outcome of a simple chemical and designing solutions rection based on the outermost electron states of atoms, trends int he periodic table, and knowl- edge of the partterns of chemi- cal properties. www.playmadagames.com ©2018 PlayMada Games LLC. All rights reserved. 1 PART 1: Explore (15 minutes) Summary This is an inquiry-driven activity where students will complete the first few levels of the Collisions Ionic Bonding game to become introduced to the concept of ionic bonding and compound ratios. Activity 1. Direct students to log into Collisions with their individual username and password. 2. Students should enter the Ionic Bonding game and play Levels 1-6 levels. 3. Have your students answer the following questions during gameplay: 1. What combination of ions did you use to successfully match a target? 2. -
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'- -
Direct Carboniiatiom of Aromatic Nttriles Using
DIRECT CARBONIIATIOM OF AROMATIC NTTRILES USING DICOBALT OCTACARBONIL by JOSEPH EDMUND GERVAX B..Sc Honours, University of Montreal, Loyola College, l?6l A THESIS SUBMITTED IN PARTIAL FUIFIIMENT OF THE REQUIREMENTS FOR THE DEGREE OF MASTER OF SCIENCE in the Department of Chemistry We accept this; thesis as conforming to the required standard THE UNIVERSITY OF BRITISH COLUMBIA June, 1963 In presenting this thesis in partial fulfilment of the requirements for an advanced degree at the University of British Columbia, I agree that the Library shall make it freely available for reference and study. I further agree that per• mission for extensive copying of this thesis for scholarly purposes may be granted by the Head of my Department or by his representatives. It is understood that copying, or publi• cation of this thesis for financial gain shall not be allowed without my written permission. Department of CHEMISTRY The University of British Columbia,. Vancouver 8, Canada. Date June 2°» W ABSTRACT A new method of synthesizing N-substituted phthalimidines is described. When benzonitrile was reacted with carbon monoxide containing about 0.0k volume percent of hydrogen and in the presence of dicobalt octacarbonyl and pyridine in benzene solution at 235° and 3U00 p.s.i. pressure the following compounds were produced: MTbenzyphthalimidine (8$), N-phenylphthalimidine (3»7%), and benzamide (3*9%)- When lj.0 p.s.i. hydrogen was added under the same reaction conditions, the yield of N-benzylphthalimidine increased (16%)., When benzonitrile was subjected to the same reaction conditions using 2U0 p.s.d* hydrogen and no pyridine, N-benzylphthalimidine (1%%) and sym-dibenzylurea (8$) were produced. -
A Study of Lithium Precursors on Nanoparticle Quality
Electronic Supplementary Material (ESI) for Nanoscale. This journal is © The Royal Society of Chemistry 2021 Electronic Supplementary Information Elucidating the role of precursors in synthesizing single crystalline lithium niobate nanomaterials: A study of lithium precursors on nanoparticle quality Rana Faryad Ali, Byron D. Gates* Department of Chemistry and 4D LABS, Simon Fraser University, 8888 University Drive Burnaby, BC, V5A 1S6, Canada * E-mail: [email protected] This work was supported in part by the Natural Sciences and Engineering Research Council of Canada (NSERC; Grant No. RGPIN-2020-06522), and through the Collaborative Health Research Projects (CHRP) Partnership Program supported in part by the Canadian Institutes of Health Research (Grant No. 134742) and the Natural Science Engineering Research Council of Canada (Grant No. CHRP 462260), the Canada Research Chairs Program (B.D. Gates, Grant No. 950-215846), CMC Microsystems (MNT Grant No. 6345), and a Graduate Fellowship (Rana Faryad Ali) from Simon Fraser University. This work made use of 4D LABS (www.4dlabs.com) and the Center for Soft Materials shared facilities supported by the Canada Foundation for Innovation (CFI), British Columbia Knowledge Development Fund (BCKDF), Western Economic Diversification Canada, and Simon Fraser University. S1 Experimental Materials and supplies All chemicals were of analytical grade and were used as received without further purification. Niobium ethoxide [Nb(OC2H5)5, >90%] was obtained from Gelest Inc., and benzyl alcohol (C7H7OH, 99%) and triethylamine [N(C2H5)3, 99.0%] were purchased from Acros Organics and Anachemia, respectively. Lithium chloride (LiCl, ~99.0%) was obtained from BDH Chemicals, and lithium bromide (LiBr, ≥99.0%), lithium fluoride (LiF, ~99.9%), and lithium iodide (LiI, 99.0%) were purchased from Sigma Aldrich. -
PAPERS READ BEFORE the CHEMICAL SOCIETY. XXII1.-On
View Article Online / Journal Homepage / Table of Contents for this issue 773 PAPERS READ BEFORE THE CHEMICAL SOCIETY. XXII1.-On Tetrabromide of Carbon. No. II. By THOMASBOLAS and CHARLESE. GROVES. IN a former paper* we described several methods for the preparation of the hitherto unknown tetrabromide of carbon, and in the present communication we desire to lay before the Society the results of our more recent experiments. In addition to those methods of obtaining the carbon tetrabromide, which we have already published, the fol- lowing are of interest, either from a theoretical point of view, or as affording advantageous means for the preparation of that substance. Action of Bromine on Carbon Disulphide. Our former statement that? bromine had no action on carbon disul- phide requires some modification, as we find that when it is heated to 180" or 200" for several hundred hours with bromine free from both chlorine and iodine, and the contents of the tubes are neutralised and distilled in the usual way, a liquid is obtained, which consists almost entirely of unaltered carbon disulphide ; but when this is allowed to evaporate spontaneously, a small quantity of a crystalline substance is left, which has the appearance and properties of carbon tetrabromide. The length of time required for this reaction, and the very small relative amount of substance obtained, would, however, render this Published on 01 January 1871. Downloaded by Brown University 25/10/2014 10:39:25. quite inapplicable as a process for the preparation of the tetra- bromide. Action of Bromine on Carbon Disdphide in, presence of Certain Bromides.