Ammonium Carbamate Hazard Summary Identification
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Modifications on the Basic Skeletons of Vinblastine and Vincristine
Molecules 2012, 17, 5893-5914; doi:10.3390/molecules17055893 OPEN ACCESS molecules ISSN 1420-3049 www.mdpi.com/journal/molecules Review Modifications on the Basic Skeletons of Vinblastine and Vincristine Péter Keglevich, László Hazai, György Kalaus and Csaba Szántay * Department of Organic Chemistry and Technology, University of Technology and Economics, H-1111 Budapest, Szt. Gellért tér 4, Hungary * Author to whom correspondence should be addressed; E-Mail: [email protected]; Tel: +36-1-463-1195; Fax: +36-1-463-3297. Received: 30 March 2012; in revised form: 9 May 2012 / Accepted: 10 May 2012 / Published: 18 May 2012 Abstract: The synthetic investigation of biologically active natural compounds serves two main purposes: (i) the total synthesis of alkaloids and their analogues; (ii) modification of the structures for producing more selective, more effective, or less toxic derivatives. In the chemistry of dimeric Vinca alkaloids enormous efforts have been directed towards synthesizing new derivatives of the antitumor agents vinblastine and vincristine so as to obtain novel compounds with improved therapeutic properties. Keywords: antitumor therapy; vinblastine; vincristine; derivatives 1. Introduction Vinblastine (1) and vincristine (2) are dimeric alkaloids (Figure 1) isolated from the Madagaskar periwinkle plant (Catharantus roseus), exhibit significant cytotoxic activity and are used in the antitumor therapy as antineoplastic agents. In the course of cell proliferation they act as inhibitors during the metaphase of the cell cycle and by binding to the microtubules inhibit the development of the mitotic spindle. In tumor cells these agents inhibit the DNA repair and the RNA synthesis mechanisms, blocking the DNA-dependent RNA polymerase. Molecules 2012, 17 5894 Figure 1. -
Carbamate Pesticides Aldicarb Aldicarb Sulfoxide Aldicarb Sulfone
Connecticut General Statutes Sec 19a-29a requires the Commissioner of Public Health to annually publish a list setting forth all analytes and matrices for which certification for testing is required. Connecticut ELCP Drinking Water Analytes Revised 05/31/2018 Microbiology Total Coliforms Fecal Coliforms/ E. Coli Carbamate Pesticides Legionella Aldicarb Cryptosporidium Aldicarb Sulfoxide Giardia Aldicarb Sulfone Carbaryl Physicals Carbofuran Turbidity 3-Hydroxycarbofuran pH Methomyl Conductivity Oxamyl (Vydate) Minerals Chlorinated Herbicides Alkalinity, as CaCO3 2,4-D Bromide Dalapon Chloride Dicamba Chlorine, free residual Dinoseb Chlorine, total residual Endothall Fluoride Picloram Hardness, Calcium as Pentachlorophenol CaCO3 Hardness, Total as CaCO3 Silica Chlorinated Pesticides/PCB's Sulfate Aldrin Chlordane (Technical) Nutrients Dieldrin Endrin Ammonia Heptachlor Nitrate Heptachlor Epoxide Nitrite Lindane (gamma-BHC) o-Phosphate Metolachlor Total Phosphorus Methoxychlor PCB's (individual aroclors) Note 1 PCB's (as decachlorobiphenyl) Note 1 Demands Toxaphene TOC Nitrogen-Phosphorus Compounds Alachlor Metals Atrazine Aluminum Butachlor Antimony Diquat Arsenic Glyphosate Barium Metribuzin Beryllium Paraquat Boron Propachlor Cadmium Simazine Calcium Chromium Copper SVOC's Iron Benzo(a)pyrene Lead bis-(2-ethylhexyl)phthalate Magnesium bis-(ethylhexyl)adipate Manganese Hexachlorobenzene Mercury Hexachlorocyclopentadiene Molybdenum Nickel Potassium Miscellaneous Organics Selenium Dibromochloropropane (DBCP) Silver Ethylene Dibromide (EDB) -
WO 2018/005077 Al O O© O
(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 2018/005077 Al 04 January 2018 (04.01.2018) W ! P O PCT (51) International Patent Classification: SC, SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, A61K 31/78 (2006.01) C08J 7/04 (2006.01) TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW. C08G 59/77 (2006.01) (84) Designated States (unless otherwise indicated, for every (21) International Application Number: kind of regional protection available): ARIPO (BW, GH, PCT/US20 17/037 176 GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, ST, SZ, TZ, UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, RU, TJ, (22) International Filing Date: TM), European (AL, AT, BE, BG, CH, CY, CZ, DE, DK, 13 June 2017 (13.06.2017) EE, ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LT, LU, LV, (25) Filing Language: English MC, MK, MT, NL, NO, PL, PT, RO, RS, SE, SI, SK, SM, TR), OAPI (BF, BJ, CF, CG, CI, CM, GA, GN, GQ, GW, (26) Publication Language: English KM, ML, MR, NE, SN, TD, TG). (30) Priority Data: 62/356,918 30 June 2016 (30.06.2016) US Published: — with international search report (Art. 21(3)) (71) Applicant: ELEMENTIS SPECIALTIES, INC. [US/US]; 469 Old Trenton Road, East Windsor, NJ 085 12 (US). (72) Inventors: IJDO, Wouter; 1224 Bridle Estates Dri ve, Yardley, PA 19067 (US). CHEN, Yanhui; 4 Hal- stead Place, Princeton, NJ 08540 (US). -
A Study on Physical Chemistry of Solid a Mmonium Materials for Nox Reduction of Diesel Engine Emissions
A Study on Physical Chemistry of Solid A mmonium Materials for NOx Reduction of Diesel Engine Emissions Cheon Seog (Steve) Yoon and Jong Kook Shin Hannam University, Daejeon, KOREA Hoyeol Lee and Hongsuk Kim Korea Institute of Machinery & Materials, Daejeon, KOREA 2014 DOE CLEERS Workshop University of Michigan, Dearborn, MI, USA 1 Table of Contents • Introduction of Solid SCR System • Ammonium Salts • Chemical Reactions, Decomposition Chemistry • Chemical Kinetic Parameters by TGA, DTA and DSC • Decomposition Rate from Hot Plate Test and Chemical Kinetic Parameters • Simple Reactor with Visible Window • Equilibrium Vapor Pressure Curve for Ammonium Carbonate • Acquisition of Re-solidified Materials from Ammonium Carbonate • Analytical Study of Re-solidified Materials from Ammonium Carbonate by XRD, FT-IR, and EA • Concluding Remarks • Acknowledgement • Reference 2 Solid SCR System • NOx purification technology by using NH3, which is generated from solid ammonium. • Ammonium carbonate, (NH4)2CO3 , is solid at room temperature, and it decomposes into NH3, H2O & CO2 above temperature of 60℃. 3 Material Properties of Ammonium Salts Solid urea Ammonium carbonate Ammonium cabarmate Molecular formula (NH2)2CO (NH4)2CO3 NH2COONH4 Molecular weight 60.07 96.09 78.07 3 Density, g/cm 1.33 1.5 1.6 Mols NH3 per Mol 2 2 2 Mols NH3 per kg 33.3 20.8 25.6 Decomposition temp., ℃ 140 58 60 NH2CONH2↔ NH3+HNCO Reaction mechanism (NH4)2CO3↔2NH3+CO2+H2O NH4COONH2 ↔ 2NH3 + CO2 HNCO +H2O ↔ NH3 + CO2 Cost cheap cheap moderate * HNCO: Isocyanic Acid [ref] G. Fulks, -
1 Abietic Acid R Abrasive Silica for Polishing DR Acenaphthene M (LC
1 abietic acid R abrasive silica for polishing DR acenaphthene M (LC) acenaphthene quinone R acenaphthylene R acetal (see 1,1-diethoxyethane) acetaldehyde M (FC) acetaldehyde-d (CH3CDO) R acetaldehyde dimethyl acetal CH acetaldoxime R acetamide M (LC) acetamidinium chloride R acetamidoacrylic acid 2- NB acetamidobenzaldehyde p- R acetamidobenzenesulfonyl chloride 4- R acetamidodeoxythioglucopyranose triacetate 2- -2- -1- -β-D- 3,4,6- AB acetamidomethylthiazole 2- -4- PB acetanilide M (LC) acetazolamide R acetdimethylamide see dimethylacetamide, N,N- acethydrazide R acetic acid M (solv) acetic anhydride M (FC) acetmethylamide see methylacetamide, N- acetoacetamide R acetoacetanilide R acetoacetic acid, lithium salt R acetobromoglucose -α-D- NB acetohydroxamic acid R acetoin R acetol (hydroxyacetone) R acetonaphthalide (α)R acetone M (solv) acetone ,A.R. M (solv) acetone-d6 RM acetone cyanohydrin R acetonedicarboxylic acid ,dimethyl ester R acetonedicarboxylic acid -1,3- R acetone dimethyl acetal see dimethoxypropane 2,2- acetonitrile M (solv) acetonitrile-d3 RM acetonylacetone see hexanedione 2,5- acetonylbenzylhydroxycoumarin (3-(α- -4- R acetophenone M (LC) acetophenone oxime R acetophenone trimethylsilyl enol ether see phenyltrimethylsilyl... acetoxyacetone (oxopropyl acetate 2-) R acetoxybenzoic acid 4- DS acetoxynaphthoic acid 6- -2- R 2 acetylacetaldehyde dimethylacetal R acetylacetone (pentanedione -2,4-) M (C) acetylbenzonitrile p- R acetylbiphenyl 4- see phenylacetophenone, p- acetyl bromide M (FC) acetylbromothiophene 2- -5- -
Environmental Protection Agency § 117.3
Environmental Protection Agency § 117.3 (4) Applicability date. This paragraph TABLE 117.3—REPORTABLE QUANTITIES OF (i) is applicable beginning on February HAZARDOUS SUBSTANCES DESIGNATED PUR- 6, 2020. SUANT TO SECTION 311 OF THE CLEAN (j) Process waste water means any WATER ACT—Continued water which, during manufacturing or Cat- RQ in pounds processing, comes into direct contact Material egory (kilograms) with or results from the production or use of any raw material, intermediate Ammonium benzoate ...................... D ...... 5,000 (2,270) Ammonium bicarbonate .................. D ...... 5,000 (2,270) product, finished product, byproduct, Ammonium bichromate ................... A ....... 10 (4.54) or waste product. Ammonium bifluoride ...................... B ....... 100 (45.4) Ammonium bisulfite ......................... D ...... 5,000 (2,270) [44 FR 50776, Aug. 29, 1979, as amended at 58 Ammonium carbamate .................... D ...... 5,000 (2,270) FR 45039, Aug. 25, 1993; 65 FR 30904, May 15, Ammonium carbonate ..................... D ...... 5,000 (2,270) 2000; 80 FR 37112, June 29, 2015; 83 FR 5208, Ammonium chloride ........................ D ...... 5,000 (2,270) Feb. 6, 2018] Ammonium chromate ...................... A ....... 10 (4.54) Ammonium citrate dibasic ............... D ...... 5,000 (2,270) Ammonium fluoborate ..................... D ...... 5,000 (2,270) § 117.2 Abbreviations. Ammonium fluoride ......................... B ....... 100 (45.4) NPDES equals National Pollutant Ammonium hydroxide ..................... C -
Chemical Name Federal P Code CAS Registry Number Acutely
Acutely / Extremely Hazardous Waste List Federal P CAS Registry Acutely / Extremely Chemical Name Code Number Hazardous 4,7-Methano-1H-indene, 1,4,5,6,7,8,8-heptachloro-3a,4,7,7a-tetrahydro- P059 76-44-8 Acutely Hazardous 6,9-Methano-2,4,3-benzodioxathiepin, 6,7,8,9,10,10- hexachloro-1,5,5a,6,9,9a-hexahydro-, 3-oxide P050 115-29-7 Acutely Hazardous Methanimidamide, N,N-dimethyl-N'-[2-methyl-4-[[(methylamino)carbonyl]oxy]phenyl]- P197 17702-57-7 Acutely Hazardous 1-(o-Chlorophenyl)thiourea P026 5344-82-1 Acutely Hazardous 1-(o-Chlorophenyl)thiourea 5344-82-1 Extremely Hazardous 1,1,1-Trichloro-2, -bis(p-methoxyphenyl)ethane Extremely Hazardous 1,1a,2,2,3,3a,4,5,5,5a,5b,6-Dodecachlorooctahydro-1,3,4-metheno-1H-cyclobuta (cd) pentalene, Dechlorane Extremely Hazardous 1,1a,3,3a,4,5,5,5a,5b,6-Decachloro--octahydro-1,2,4-metheno-2H-cyclobuta (cd) pentalen-2- one, chlorecone Extremely Hazardous 1,1-Dimethylhydrazine 57-14-7 Extremely Hazardous 1,2,3,4,10,10-Hexachloro-6,7-epoxy-1,4,4,4a,5,6,7,8,8a-octahydro-1,4-endo-endo-5,8- dimethanonaph-thalene Extremely Hazardous 1,2,3-Propanetriol, trinitrate P081 55-63-0 Acutely Hazardous 1,2,3-Propanetriol, trinitrate 55-63-0 Extremely Hazardous 1,2,4,5,6,7,8,8-Octachloro-4,7-methano-3a,4,7,7a-tetra- hydro- indane Extremely Hazardous 1,2-Benzenediol, 4-[1-hydroxy-2-(methylamino)ethyl]- 51-43-4 Extremely Hazardous 1,2-Benzenediol, 4-[1-hydroxy-2-(methylamino)ethyl]-, P042 51-43-4 Acutely Hazardous 1,2-Dibromo-3-chloropropane 96-12-8 Extremely Hazardous 1,2-Propylenimine P067 75-55-8 Acutely Hazardous 1,2-Propylenimine 75-55-8 Extremely Hazardous 1,3,4,5,6,7,8,8-Octachloro-1,3,3a,4,7,7a-hexahydro-4,7-methanoisobenzofuran Extremely Hazardous 1,3-Dithiolane-2-carboxaldehyde, 2,4-dimethyl-, O- [(methylamino)-carbonyl]oxime 26419-73-8 Extremely Hazardous 1,3-Dithiolane-2-carboxaldehyde, 2,4-dimethyl-, O- [(methylamino)-carbonyl]oxime. -
Amino Acid Metabolism, Urea Cycle Semester Iv, Paper Cc8
AMINO ACID METABOLISM, UREA CYCLE SEMESTER IV, PAPER CC8 UREA CYCLE + Some of the NH4 formed in the breakdown of amino acids is consumed in the biosynthesis of nitrogen compounds. Most aquatic species, such as the bony fishes, are ammonotelic, excreting amino nitrogen as ammonia. The toxic ammonia is simply diluted in the surrounding water. Most terrestrial animals are ureotelic, excreting amino nitrogen in the form of urea; birds and reptiles are uricotelic, excreting amino nitrogen as uric acid. In ureotelic organisms, the ammonia deposited in the mitochondria of hepatocytes is converted to urea in the urea cycle. This pathway was discovered in 1932 by Hans Krebs. The urea cycle begins inside liver mitochondria, but three of the subsequent steps take place in the cytosol. The first amino group to enter the urea cycle is derived from ammonia in the mitochondrial matrix arising from various amino acids. The urea cycle begins with the coupling of free NH4 + with HCO3- to form carbamoyl phosphate. The synthesis of carbamoyl phosphate, though a simple molecule, is complex, comprising three steps, all catalyzed by carbamoyl phosphate synthetase. - The reaction begins with the phosphorylation of HCO3 to form carboxyphosphate, which then reacts with ammonium ion to form carbamic acid. Finally, a second molecule of ATP phosphorylates carbamic acid to carbamoyl phosphate. The consumption of two molecules of ATP makes this synthesis of carbamoyl phosphate essentially irreversible. Next, the carbamoyl group of carbamoyl phosphate, which has a high transfer potential because of its anhydride bond, is transferred to ornithine to form citrulline, in a reaction catalyzed by + ornithine transcarbamoylase. -
United States Patent (19) 11 Patent Number: 5,788,915 Blount (45) Date of Patent: Aug
IIIUSOO5788915A United States Patent (19) 11 Patent Number: 5,788,915 Blount (45) Date of Patent: Aug. 4, 1998 54 FLAME RETARDANT COMPOSITIONS 57 ABSTRACT UTILIZING PARTIALLY HYDROLYZED AMNO CONDENSATON COMPOUNDS Flame retardant compositions of this invention are produced by incorporating a partially index (LOI) hydrolyzed amino 76 Inventor: David H. Blount, 6728 Del Cerro condensation composition in a more flammable organic Blvd., San Diego, Calif. 92120 material. The partially hydrolyzed amino condensation com pounds are produced by heating urea or heating urea with (21) Appl. No.: 801,776 other nitrogen containing compounds that will condensate with or react with isocyanic acid and/or cyanic acid thereby 22 Filed: Feb. 14, 1997 producing an amino condensation compound which is then Related U.S. Application Data partially hydrolysis is done by reacting it with a limited amount of water. The partially hydrolyzed amino conden 62) Division of Ser. No. 723,779, Sep. 30, 1996. sation compounds may be used alone or may be mixed with or reacted with carbonization auxiliaries, aldehydes and (51) Int. Cl. ........................ C09K 21A00; C08G 12/12 fillers to produce a partially hydrolyzed amino condensation 52 U.S. Cl. ........................... 252/609; 528/259; 252/601 composition which is incorporated in more flammable 58) Field of Search ..................................... 252/609, 601: organic compositions such as polyurethanes, polyester 528/259 resins. epoxy resins, vinyl resins and other resins. The partially hydrolyzed amino condensation salts of 56 References Cited phosphorus, boron or sulfur containing compounds and the U.S. PATENT DOCUMENTS partially hydrolyzed amino condensation-aldehyde resins 3,900,665 8/1975 Weil ....................................... -
N-Methyl Carbamate Cumulative Risk Assessment: Pilot Cumulative Analysis
UNITED STATES ENVIRONMENTAL PROTECTION AGENCY WASHINGTON, D.C. 20460 OFFICE OF PREVENTION, PESTICIDES, AND TOXIC SUBSTANCES April 15, 2005 MEMORANDUM SUBJECT: Transmittal of Meeting Minutes of the FIFRA Scientific Advisory Panel Meeting Held February 15 - 18, 2005 on the N-methyl Carbamate Cumulative Risk Assessment: Pilot Cumulative Analysis TO: James J. Jones, Director Office of Pesticide Programs FROM: Myrta R. Christian, Designated Federal Official Joseph E. Bailey, Designated Federal Official FIFRA Scientific Advisory Panel Office of Science Coordination and Policy THRU: Larry C. Dorsey, Executive Secretary FIFRA Scientific Advisory Panel Office of Science Coordination and Policy Clifford J. Gabriel, Director Office of Science Coordination and Policy Attached, please find the meeting minutes of the FIFRA Scientific Advisory Panel open meeting held in Arlington, Virginia on February 15 - 18, 2005. This report addresses a set of scientific issues being considered by the Environmental Protection Agency pertaining to the N- methyl carbamate cumulative risk assessment: pilot cumulative analysis. Attachment 1 of 113 cc: Susan Hazen Margaret Schneider Anne Lindsay Margie Fehrenbach Janet Andersen Debbie Edwards Steven Bradbury William Diamond Arnold Layne Tina Levine Lois Rossi Frank Sanders Richard Keigwin Randolph Perfetti William Jordan Douglas Parsons Enesta Jones Vanessa Vu (SAB) Anna Lowit David J. Miller Nelson Thurman Dirk Young David Hrdy Jeff Evans Steve Nako Stephanie Padilla R. Woodrow Setzer Ginger Moser Miles Okino Jerry Blancato Fred Power Curtis Dary Tom Nolan, USGS OPP Docket 2 of 113 FIFRA Scientific Advisory Panel Members Stephen M. Roberts, Ph.D. (Chair of the FIFRA SAP) Janice E. Chambers, Ph.D. H. Christopher Frey, Ph.D. -
Ammonium Carbonate. Drogen in Chlorine Is Dissolved in Water and Then Reacted with Gaseous Ammo- (A) Ammonium Carbonate ((NH4)2CO3, Nia
Food and Drug Administration, HHS § 184.1138 (1) The ingredient is used as a dough (d) Prior sanctions for this ingredient strengthener as defined in § 170.3(o)(6) different from the uses established in of this chapter; a leavening agent as this section do not exist or have been defined in § 170.3(o)(17) of this chapter; waived. a pH control agent as defined in § 170.3(o)(23) of this chapter; and a [48 FR 52439, Nov. 18, 1983] texturizer as defined in § 170.3(o)(32) of § 184.1138 Ammonium chloride. this chapter. (2) The ingredient is used in food at (a) Ammonium chloride (NH4Cl, CAS levels not to exceed current good man- Reg. No. 12125–02–9) is produced by the ufacturing practice. reaction of sodium chloride and an am- (d) Prior sanctions for this ingredient monium salt in solution. The less solu- different from the uses established in ble sodium salt separates out at ele- this section do not exist or have been vated temperatures, and ammonium waived. chloride is recovered from the filtrate on cooling. Alternatively, hydrogen [48 FR 52439, Nov. 18, 1983] chloride formed by the burning of hy- § 184.1137 Ammonium carbonate. drogen in chlorine is dissolved in water and then reacted with gaseous ammo- (a) Ammonium carbonate ((NH4)2CO3, nia. Ammonium chloride is crystallized CAS Reg. No. 8000–73–5) is a mixture of from the solution. ammonium bicarbonate (NH4HCO3) and (b) The ingredient meets the speci- ammonium carbamate (NH2COONH4). fications of the Food Chemicals Codex, It is prepared by the sublimation of a 3d Ed. -
Selective Effects of Carbamate Pesticides on Rat Neuronal Nicotinic Acetylcholine Receptors and Rat Brain Acetylcholinesterase Chantal J.G.M
Available online at www.sciencedirect.com R Toxicology and Applied Pharmacology 193 (2003) 139–146 www.elsevier.com/locate/taap Selective effects of carbamate pesticides on rat neuronal nicotinic acetylcholine receptors and rat brain acetylcholinesterase Chantal J.G.M. Smulders,a Tjerk J.H. Bueters,b Regina G.D.M. Van Kleef,a and Henk P.M. Vijverberga,* a Institute for Risk Assessment Sciences, Utrecht University, P.O. Box 80176, NL-3508 TD Utrecht, The Netherlands b TNO Prins Maurits Laboratory, P.O. Box 45, NL-2280 AA Rijswijk, The Netherlands Received 14 May 2003; accepted 31 July 2003 Abstract Effects of commonly used carbamate pesticides on rat neuronal nicotinic acetylcholine receptors expressed in Xenopus laevis oocytes have been investigated using the two-electrode voltage clamp technique. The potencies of these effects have been compared to the potencies of the carbamates to inhibit rat brain acetylcholinesterase. The potency order of six carbamates to inhibit ␣44 nicotinic receptors is fenoxycarb Ͼ EPTC Ͼ carbaryl, bendiocarb Ͼ propoxur Ͼ aldicarb with IC50 values ranging from 3 M for fenoxycarb to 165 M for propoxur and Ͼ1 mM for aldicarb. Conversely, the potency order of these carbamates to inhibit rat brain acetylcholinesterase is bendiocarb Ͼ propoxur, aldicarb Ͼ carbaryl ϾϾ EPTC, fenoxycarb with IC50 values ranging from 1 M for bendiocarb to 17 M for carbaryl and ϾϾ1 mM for EPTC and fenoxycarb. The ␣42, ␣34, and ␣32 nicotinic acetylcholine receptors are inhibited by fenoxycarb, EPTC, and carbaryl with potency orders similar to that for ␣44 receptors. Comparing the potencies of inhibition of the distinct subtypes of nicotinic acetylcholine receptors shows that the ␣32 receptor is less sensitive to inhibition by fenoxycarb and EPTC.