Toxicological Profile for Antimony
Total Page:16
File Type:pdf, Size:1020Kb

Load more
Recommended publications
-
Tartaric Acid
TECHNICAL DATA SHEET SPECIFIC TREATMENTS TARTARIC ACID Acidity regulator COMPOSITION L (+) tartaric acid (E334) APPLICATIONS ▪ Acid correction in wine and juice. ▪ Treatment of tanks and concrete containers. DOSAGE Fresh grapes, partially fermented must, fermenting wien limited to wine-growing zones C I, C II, C III a and C III b: up to a limit of 150 g/hL. (except for exceptions). In wine: up to 250 g/hL (except for exceptions and always limited to the above-mentioned zones). In the European Union, it is allowed to acidify must and wine with tartaric acid together with L-lactic acid, L-malic acid and DL-malic acid. In case other organic acids are used in the same must or wine, it is necessary to calculate the maximum amount of tartaric acid that can be used in compliance with the limits set by the regulation. For countries outside Europe, please refer to local regulations. USA: Legal Limits 9.0 grams per liter. In cases where the wine contains 8.0 or more grams of total solids per 100 milliliters of wine, acids may be added to the extent that the finished wine does not contain more than 11.0 grams per liter of fixed acid (calculated as tartaric acid). INSTRUCTIONS FOR USE Dissolve directly into a small amount of must or wine and add uniformly to the mass to be treated. PACKAGING AND STORAGE CONDITIONS 1 kg, 25 kg Sealed package: store in a cool, dry, well-ventilated area. Open package: carefully reseal and store it as indicated above. COMPLIANCE The product is in compliance with: Codex Œnologique International Reg. -
An Investigation of the Crystal Growth of Heavy Sulfides in Supercritical
AN ABSTRACT OF THE THESIS OF LEROY CRAWFORD LEWIS for the Ph. D. (Name) (Degree) in CHEMISTRY presented on (Major) (Date) Title: AN INVESTIGATION OF THE CRYSTAL GROWTH OF HEAVY SULFIDES IN SUPERCRITICAL HYDROGEN SULFIDE Abstract approved Redacted for privacy Dr. WilliarriIJ. Fredericks Solubility studies on the heavy metal sulfides in liquid hydrogen sulfide at room temperature were carried out using the isopiestic method. The results were compared with earlier work and with a theoretical result based on Raoult's Law. A relative order for the solubilities of sulfur and the sulfides of tin, lead, mercury, iron, zinc, antimony, arsenic, silver, and cadmium was determined and found to agree with the theoretical result. Hydrogen sulfide is a strong enough oxidizing agent to oxidize stannous sulfide to stannic sulfide in neutral or basic solution (with triethylamine added). In basic solution antimony trisulfide is oxi- dized to antimony pentasulfide. In basic solution cadmium sulfide apparently forms a bisulfide complex in which three moles of bisul- fide ion are bonded to one mole of cadmium sulfide. Measurements were made extending the range over which the volumetric properties of hydrogen sulfide have been investigated to 220 °C and 2000 atm. A virial expression in density was used to represent the data. Good agreement, over the entire range investi- gated, between the virial expressions, earlier work, and the theorem of corresponding states was found. Electrical measurements were made on supercritical hydro- gen sulfide over the density range of 10 -24 moles per liter and at temperatures from the critical temperature to 220 °C. Dielectric constant measurements were represented by a dielectric virial ex- pression. -
Resolution of Racemic Amphetamines Into D- and L-Amphetamines - Dru
Resolution of Racemic Amphetamines into d- and l-Amphetamines - Dru... http://www.drugs-forum.co.uk/forum/showthread.php?t=37740&highlig... Drugs Forum > Forum > VARIOUS DRUG RELATED TOPICS > Drug Welcome, Quantum Dude. You last visited: 11-05-2007 at 11:56 AM related chemistry and extraction > Phenethylamine Chemistry > Private Messages: Unread 0, Total 11. Methamphetamine Chemistry Resolution of Racemic Amphetamines into d- and l-Amphetamines User CP FAQ n Rules Radio Stations New Posts Search Quick Links Log Out Methamphetamine Chemistry Discussion of the synthesis of methamphetamine Thread Tools Search this Thread Rate Thread Display Modes 08-26-2007, 07:16 PM #1 Join Date: Jun 2007 Location: Europe Age: 22 outriderx Donating Silver Member Posts: 109 Resolution of Racemic Amphetamines into d- and l-Amphetamines Contents 1 Methamphetamine Optical Resolution by Distillation After Partial Diastereoisomeric Salt Formation 2 Dutch Resolution: Separation of Enantiomers with Families of Resolving Agents. A Status Report 1 Resolution of racemic Amphetamine 2 Resolution of racemic Methamphetamine 3 Resolution of racemic Amphetamine 4 Resolution of racemic Methamphetamine using selective extraction 5 Resolution of racemic Methamphetamine using O,O-Dibenzoyl-R,R-Tartaric Acid Methamphetamine Optical Resolution by Distillation After Partial Diastereoisomeric [top] Salt Formation Solvent-free optical resolution of N-methylamphetamine was developed by distillation after partial diastereoisomeric salt formation. From the 18 chiral acids tested by this method, five provide by this method resolution: O,O'-dibenzoyltartaric acid, O,O'-di-p-toluoyltartaric acid, 6-methoxy-alpha-methyl-2-naphthaleneacetic acid (Naproxen), the cis-permetrinic acid, and the 2-phenoxypropionic acid. Among them the O,O'-dibenzoyltartaric acid in water-free form 1 of 7 05/11/2007 4:02 PM Resolution of Racemic Amphetamines into d- and l-Amphetamines - Dru.. -
Classification of Medicinal Drugs and Driving: Co-Ordination and Synthesis Report
Project No. TREN-05-FP6TR-S07.61320-518404-DRUID DRUID Driving under the Influence of Drugs, Alcohol and Medicines Integrated Project 1.6. Sustainable Development, Global Change and Ecosystem 1.6.2: Sustainable Surface Transport 6th Framework Programme Deliverable 4.4.1 Classification of medicinal drugs and driving: Co-ordination and synthesis report. Due date of deliverable: 21.07.2011 Actual submission date: 21.07.2011 Revision date: 21.07.2011 Start date of project: 15.10.2006 Duration: 48 months Organisation name of lead contractor for this deliverable: UVA Revision 0.0 Project co-funded by the European Commission within the Sixth Framework Programme (2002-2006) Dissemination Level PU Public PP Restricted to other programme participants (including the Commission x Services) RE Restricted to a group specified by the consortium (including the Commission Services) CO Confidential, only for members of the consortium (including the Commission Services) DRUID 6th Framework Programme Deliverable D.4.4.1 Classification of medicinal drugs and driving: Co-ordination and synthesis report. Page 1 of 243 Classification of medicinal drugs and driving: Co-ordination and synthesis report. Authors Trinidad Gómez-Talegón, Inmaculada Fierro, M. Carmen Del Río, F. Javier Álvarez (UVa, University of Valladolid, Spain) Partners - Silvia Ravera, Susana Monteiro, Han de Gier (RUGPha, University of Groningen, the Netherlands) - Gertrude Van der Linden, Sara-Ann Legrand, Kristof Pil, Alain Verstraete (UGent, Ghent University, Belgium) - Michel Mallaret, Charles Mercier-Guyon, Isabelle Mercier-Guyon (UGren, University of Grenoble, Centre Regional de Pharmacovigilance, France) - Katerina Touliou (CERT-HIT, Centre for Research and Technology Hellas, Greece) - Michael Hei βing (BASt, Bundesanstalt für Straßenwesen, Germany). -
Material Safety Data Sheet
Material Safety Data Sheet Antimony trichloride, reagent ACS, crystals, 99+% ACC# 00252 Section 1 - Chemical Product and Company Identification MSDS Name: Antimony trichloride, reagent ACS, crystals, 99+% Catalog Numbers: AC401370000, AC401370050, AC401371000, AC401375000 Synonyms: Trichlorostibine; Antimonous chloride; Antimony(III) chloride; Antimony trichloride. Company Identification: Acros Organics N.V. One Reagent Lane Fair Lawn, NJ 07410 For information in North America, call: 800-ACROS-01 For emergencies in the US, call CHEMTREC: 800-424-9300 Section 2 - Composition, Information on Ingredients CAS# Chemical Name Percent EINECS/ELINCS 10025-91-9 Antimony(III) chloride >99 233-047-2 Section 3 - Hazards Identification EMERGENCY OVERVIEW Appearance: white solid. Danger! Corrosive. Causes severe eye and skin burns. Causes severe digestive and respiratory tract burns. May be harmful if swallowed. Moisture sensitive. Hygroscopic (absorbs moisture from the air). Target Organs: Lungs, cardiovascular system, eyes, skin, mucous membranes. Potential Health Effects Eye: Causes eye burns. Skin: Causes skin burns. Ingestion: Causes gastrointestinal tract burns. May be harmful if swallowed. Inhalation: Causes chemical burns to the respiratory tract. May cause lung damage. May produce cardiovascular effects. Chronic: Chronic exposure may cause liver damage. Section 4 - First Aid Measures Eyes: In case of contact, immediately flush eyes with plenty of water for a t least 15 minutes. Get medical aid immediately. Skin: In case of contact, immediately flush skin with plenty of water for at least 15 minutes while removing contaminated clothing and shoes. Get medical aid immediately. Wash clothing before reuse. Ingestion: If swallowed, do NOT induce vomiting. Get medical aid immediately. If victim is fully conscious, give a cupful of water. -
Generation of Carbon Dioxide and Mobilization of Antimony Trioxide by Fungal Decomposition of Building Materials John D
University of South Florida Scholar Commons Graduate Theses and Dissertations Graduate School 3-25-2005 Generation of Carbon Dioxide and Mobilization of Antimony Trioxide by Fungal Decomposition of Building Materials John D. Krause University of South Florida Follow this and additional works at: https://scholarcommons.usf.edu/etd Part of the American Studies Commons Scholar Commons Citation Krause, John D., "Generation of Carbon Dioxide and Mobilization of Antimony Trioxide by Fungal Decomposition of Building Materials" (2005). Graduate Theses and Dissertations. https://scholarcommons.usf.edu/etd/730 This Dissertation is brought to you for free and open access by the Graduate School at Scholar Commons. It has been accepted for inclusion in Graduate Theses and Dissertations by an authorized administrator of Scholar Commons. For more information, please contact [email protected]. Generation of Carbon Dioxide and Mobilization of Antimony Trioxide by Fungal Decomposition of Building Materials by John D. Krause A dissertation submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy Department of Environmental and Occupational Health College of Public Health University of South Florida Major Professor: Yehia Y. Hammad, Sc.D. Noreen D. Poor, Ph.D. Ann C. Debaldo, Ph.D. Diane Te Strake, Ph.D. Date of Approval: March 25, 2005 Keywords: mold, mould, carbon dioxide, antimony trioxide, flame retardant © Copyright 2005, John D. Krause Dedication For their love, support, patience and understanding throughout this endeavor, I dedicate this work to my family, daughter, and most of all, my loving wife. Acknowledgements I would like to acknowledge the following individuals and companies for their assistance in this research. -
Gsaüiiveiwibte
'C or GSAÜIIVEIWIBTE CUflIIITIIIi MïtiTHI AJIAlfïïf ,7 -' y/ . •'• .'7. 's -i, . \ STELLINGEN BEHORENDE BIJ HEJ FROEFSCHRIffT VAN R. FURLER 1. De episoomtheorie over het ontstaan van het mitochon- drion is weinig plausibel. R.A, Ratt and H.R. Mahler, Science 221 O972),575 2, Doordat S. Cirendini et al. de dragergassnelheid aan 'aet einde van een chromatografische kolom gebruiken, ontstaat een geflatteerd beeld van de weergegeven re- sultaten. Tevens is het niet mogelijk een dragergas- snelheid te berekenen zonder dat men de interstitiële porositeit kent» S, Cirendini, J. Vermont, J.C. Gressin and CL. Guilleain , J. Chromat. 84 (1973),24 3. De in de mode zijnde bepaling van RNA-moleculair ge- wichten door metingen aan formaldehyde behandelde RNA's berust op dubieuze aannamen. J.M. Kaper and M.E. v/aterworth,Virology 51 (1973),183 T.O. Diener and D.R. Smith, Virology *£ (^973), 359 M.M. El Manna and G. Bruening, Virology 56 (1973),198 4, Op grond van de zeer grote verschillen in stralingska- rakteristiek van de isotopen 1-131 en 1-123 is het streven van isotopenproducenten om een zo 'schoon' mogelijk 1-123 voor diagnostische doeleinden te leve- ren in strijd met de volksgezondheid, doordat de ver- tragingen#die dit oplevert onnodige stralingsbelasting voor patiënten veroorzaakt. H. ïlishiyama et al. J.Nucl.Med. 1£ (1974),261 5« De analogie die Gilbert et al. opmerken tussen de "exchange peak" in de kolom vloaistofchromatografie met behulp van ionenwisselaar en de luchtpi.ek bij gaschromatografie is twijfelachtig. T.W. Gilbert and R.A, Dobbs, Analyt.Chem. 45 (1>73), 1390. -
4. Inorganic Flame Retardants. Plastics Can Be Given Flame Retardant Characteristics by Introducing Elements of Organic, Inorganic and Halogen Origin
4. Inorganic Flame Retardants. Plastics can be given flame retardant characteristics by introducing elements of organic, inorganic and halogen origin. Such elements include magnesium, aluminium, phosphorous, molybdenum, antimony, tin, chlorine and bromine. Flame retardants are added in either the manufacturing step of the polymer or the compounding step of the polymeric article. Phosphorous bromine and chlorine are usually included as some organic compound. Inorganic flame retardants are usually added together with other flame retardants to provide a more efficient flame retardant action through synergism. Halogen flame retardants usually need an addition of about 40% in order to be effective, and this affects the properties of the polymer quite negatively. Structural integrity of the polymer article is often very important, and a drastic decrease in strength and other mechanical properties is simply not acceptable. The efficiency of halogen flame retardants is often enhanced by the addition of inorganic flame retardants. A smaller mass percentage halogen flame retardant is now needed, so the adverse effect on the polymer properties is also reduced (Touval, 1993) . 4.1 Antimony Compounds The antimony compounds used for flame retardancy include antimony trioxide, antimony pentoxide and antimony-metal compounds. In 1990 in the United States alone, the use of antimony trioxide amounted to 20 000 metric tons just for the flame retardancy of plastics. Antimony oxide is readily found in nature but in very impure form. This is not suitable for 29 direct use as flame retardant, so antimony oxide is often rather produced from antimony metal. There are therefore many different grades of antimony oxide that can be used for flame retardants. -
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. -
CAS No.) Screening Justification Is Public Comment Now Open? CAS No
EGLE Air Quality Division (AQD) Air Toxics Screening Level Justifications (Numerically by CAS No.) Screening Justification Is Public Comment Now Open? CAS No. Chemical Name Level & Responses Info E-Mail AQD Deadline None ad acid View View Not Open for Public Comment None amyl acetate (mixture) View View Not Open for Public Comment None atlox 848 View View Not Open for Public Comment None biosam tp-1.5 View View Not Open for Public Comment None calcium chloride View View Not Open for Public Comment None epoxy resin solution View View Not Open for Public Comment None heptamethyl-1-vinyl-1,7-dichlorotetrasilazane View View Not Open for Public Comment None n-butylglucamine View View Not Open for Public Comment None n-chloro-2,6-difluorobenzamide View View Not Open for Public Comment None trichloroethylene View View Not Open for Public Comment None triethylammonium suleptanate View View Not Open for Public Comment 50-00-0 formaldehyde View View Not Open for Public Comment 50-03-3 hydrocortisone acetate View View Not Open for Public Comment 50-21-5 lactic acid View View Not Open for Public Comment 50-28-2 estradiol View View Not Open for Public Comment 50-29-3 ddt View View Not Open for Public Comment 50-32-8 benzo(a)pyrene View View Not Open for Public Comment 51-28-5 2,4-dinitrophenol View View Not Open for Public Comment 53-36-1 methyl predisolone acetate View View Not Open for Public Comment 53-70-3 dibenz(a,h)anthracene View View Not Open for Public Comment 56-23-5 carbon tetrachloride View View Not Open for Public Comment 56-49-5 3-methylcholanthrene View View Not Open for Public Comment 56-55-3 benz(a)anthracene View View Not Open for Public Comment 56-81-5 glycerol View View Not Open for Public Comment 57-11-4 stearic acid View View Not Open for Public Comment Revised Monday, September 27, 2021 Page 1 of 51 EGLE Air Quality Division (AQD) Air Toxics Screening Level Justifications (Numerically by CAS No.) Screening Justification Is Public Comment Now Open? CAS No. -
Properties and Human Exposure; Sanford Garner; Roc; Jan. 24, 2018
Draft RoC Monograph on Antimony Trioxide Properties and Human Exposure Sanford Garner, PhD Integrated Laboratory Systems, Inc. Contractor supporting the Office of the Report on Carcinogens National Institute of Environmental Health Sciences January 24, 2018 Properties Antimony and antimony compounds • Antimony is a metalloid found in nature in over 100 mineral species – Exists as four oxidation states: -3, 0, +3 and +5 • +3 (trivalent) and +5 (pentavalent) are most common in environmental, biological, and geochemical systems – Antimony species can undergo transformation during manufacturing processes, in the environment, or in vivo • Elemental antimony is a silver-white metal used to make alloys • Antimony(III) trioxide exists as an odorless white powder or polymorphic crystals Properties Solubility of antimony oxides and antimony metal is higher in biological fluids than in water • Antimony trioxide: 3.3 mg/L in water • Antimony pentoxide: 0.043 mg/L in water • Antimony metal: Insoluble in water Source: ECHA Registration Dossiers for diantimony pentoxide and diantimony trioxide. Properties and Human Exposure Human Exposure Human Exposure A significant number of people in the United States are exposed to antimony(III) trioxide based on: • Consumption (~ 70 million lb/yr; 1 producer and 10 importers reported in the United States) in manufacturing • Widespread use in industrial applications (e.g., 273 companies in the flame retardant industry) • Occupational exposure • General population exposure – Consumer products – Environmental exposure Uses of Antimony(III) Trioxide Antimony(III) trioxide is the most commercially significant form of processed antimony • Workers in formulation, processing, and manufacturing of consumer products are exposed to antimony(III) trioxide Consumer Formulation Processing products flame retardant e.g., furniture, flame retardant plastics (including electrical and synergist PVC), textiles, electronic equipment rubbers e.g., PET containers PET packaging and PET catalyst for water, soft drinks, fibers etc. -
123. Antimony
1998:11 The Nordic Expert Group for Criteria Documentation of Health Risks from Chemicals 123. Antimony John Erik Berg Knut Skyberg Nordic Council of Ministers arbete och hälsa vetenskaplig skriftserie ISBN 91–7045–471–x ISSN 0346–7821 http://www.niwl.se/ah/ah.htm National Institute for Working Life National Institute for Working Life The National Institute for Working Life is Sweden's center for research and development on labour market, working life and work environment. Diffusion of infor- mation, training and teaching, local development and international collaboration are other important issues for the Institute. The R&D competence will be found in the following areas: Labour market and labour legislation, work organization and production technology, psychosocial working conditions, occupational medicine, allergy, effects on the nervous system, ergonomics, work environment technology and musculoskeletal disorders, chemical hazards and toxicology. A total of about 470 people work at the Institute, around 370 with research and development. The Institute’s staff includes 32 professors and in total 122 persons with a postdoctoral degree. The National Institute for Working Life has a large international collaboration in R&D, including a number of projects within the EC Framework Programme for Research and Technology Development. ARBETE OCH HÄLSA Redaktör: Anders Kjellberg Redaktionskommitté: Anders Colmsjö och Ewa Wigaeus Hjelm © Arbetslivsinstitutet & författarna 1998 Arbetslivsinstitutet, 171 84 Solna, Sverige ISBN 91–7045–471–X ISSN 0346-7821 Tryckt hos CM Gruppen Preface The Nordic Council is an intergovernmental collaborative body for the five countries, Denmark, Finland, Iceland, Norway and Sweden. One of the committees, the Nordic Senior Executive Committee for Occupational Environmental Matters, initiated a project in order to produce criteria documents to be used by the regulatory authorities in the Nordic countries as a scientific basis for the setting of national occupational exposure limits.