Safety Data Sheet SODIUM BISULFITE
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Sodium Chlorite Neutralization
® Basic Chemicals Sodium Chlorite Neutralization Introduction that this reaction is exothermic and liberates a If sodium chlorite is spilled or becomes a waste, significant amount of heat (H). it must be disposed of in accordance with local, state, and Federal regulations by a NPDES NaClO2 + 2Na2SO3 2Na2SO4 + NaCl permitted out-fall or in a permitted hazardous 90.45g + 2(126.04g) 2(142.04g) + 58.44g waste treatment, storage, and disposal facility. H = -168 kcal/mole NaClO2 Due to the reactivity of sodium chlorite, neutralization for disposal purposes should be For example, when starting with a 5% NaClO2 avoided whenever possible. Where permitted, solution, the heat generated from this reaction the preferred method for handling sodium could theoretically raise the temperature of the chlorite spills and waste is by dilution, as solution by 81C (146F). Adequate dilution, discussed in the OxyChem Safety Data Sheet thorough mixing and a slow rate of reaction are (SDS) for sodium chlorite in Section 6, important factors in controlling the temperature (Accidental Release Measures). Sodium chlorite increase (T). neutralization procedures must be carried out only by properly trained personnel wearing Procedure appropriate protective equipment. The complete neutralization procedure involves three sequential steps: dilution, chlorite Reaction Considerations reduction, and alkali neutralization. The dilution If a specific situation requires sodium chlorite to step lowers the strength of the sodium chlorite be neutralized, the chlorite must first be reduced solution to 5% or less; the reduction step reacts by a reaction with sodium sulfite. The use of the diluted chlorite solution with sodium sulfite to sodium sulfite is recommended over other produce a sulfate solution, and the neutralization reducing agents such as sodium thiosulfate step reduces the pH of the alkaline sulfate (Na2S2O3), sodium bisulfite (NaHSO3), and solution from approximately 12 to 4-5. -
Reregistration Eligibility Decision (RED) for Inorganic Sulfites
Reregistration Eligibility Decision – Inorganic Sulfites May 2007 Reregistration Eligibility Decision Inorganic Sulfites Special Review and Reregistration Division Office of Pesticide Programs U.S. Environmental Protection Agency 1801 South Bell Street Arlington, VA 22202 Introduction The Environmental Protection Agency (EPA) has completed its Reregistration Eligibility Decision (RED) for the inorganic sulfites case, which includes the chemicals sulfur dioxide and sodium metabisulfite. This assessment provides information to support the issuance of a Reregistration Eligibility Decision for inorganic sulfites. EPA’s pesticide reregistration process provides for the review of older pesticides (those initially registered prior to November 1984) under the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA) to ensure that they meet current scientific and regulatory standards. In this document, EPA presents the results of its review of the potential human health effects of dietary, drinking water and occupational/bystander exposure to inorganic sulfites, as well as its ecological risk findings. Evaluations performed by the World Health Organization (WHO), the International Agency for Research on Cancer (IARC), and the Agency for Toxic Substances and Disease Registry (ATSDR) were relied upon for this assessment, in addition to peer-reviewed evaluations performed by the Cosmetic Ingredient Review (CIR), the Organization for Economic Cooperation and Development-Screening Information Data Set (OECD-SIDS) and from other open literature sources. Based on this assessment, the Agency has determined that products containing sulfur dioxide or sodium metabisulfite are eligible for reregistration provided the necessary label changes are made. As a result of this assessment, one tolerance has been reassessed. I. Use Information The inorganic sulfites reregistration case includes the chemicals sulfur dioxide (CAS No. -
DNA Methylation Analysis: Choosing the Right Method
biology Review DNA Methylation Analysis: Choosing the Right Method Sergey Kurdyukov 1,* and Martyn Bullock 2 Received: 8 July 2015; Accepted: 22 December 2015; Published: 6 January 2016 Academic Editor: Melanie Ehrlich 1 Genomics Core facility, Kolling Institute of Medical Research, University of Sydney, Sydney 2065, Australia 2 Cancer Genetics Laboratory, Kolling Institute of Medical Research, University of Sydney, Sydney 2065, Australia; [email protected] * Correspondence: [email protected]; Tel.: +61-299-264-756 Abstract: In the burgeoning field of epigenetics, there are several methods available to determine the methylation status of DNA samples. However, choosing the method that is best suited to answering a particular biological question still proves to be a difficult task. This review aims to provide biologists, particularly those new to the field of epigenetics, with a simple algorithm to help guide them in the selection of the most appropriate assay to meet their research needs. First of all, we have separated all methods into two categories: those that are used for: (1) the discovery of unknown epigenetic changes; and (2) the assessment of DNA methylation within particular regulatory regions/genes of interest. The techniques are then scrutinized and ranked according to their robustness, high throughput capabilities and cost. This review includes the majority of methods available to date, but with a particular focus on commercially available kits or other simple and straightforward solutions that have proven to be useful. Keywords: DNA methylation; 5-methylcytosine; CpG islands; epigenetics; next generation sequencing 1. Introduction DNA methylation in vertebrates is characterized by the addition of a methyl or hydroxymethyl group to the C5 position of cytosine, which occurs mainly in the context of CG dinucleotides. -
“Inactive” Ingredients in Pharmaceutical Products: Update (Subject Review)
AMERICAN ACADEMY OF PEDIATRICS Committee on Drugs “Inactive” Ingredients in Pharmaceutical Products: Update (Subject Review) ABSTRACT. Because of an increasing number of re- bronchospasm from antiasthmatic drugs, aspartame- ports of adverse reactions associated with pharmaceutical induced headache and seizures, saccharin-induced excipients, in 1985 the Committee on Drugs issued a cross-sensitivity reactions in children with sulfon- position statement1 recommending that the Food and amide allergy, benzyl alcohol toxicity in neonates Drug Administration mandate labeling of over-the- receiving high-dose continuous infusion with pre- counter and prescription formulations to include a qual- served medications, dye-related cross-reactions in itative list of inactive ingredients. However, labeling of inactive ingredients remains voluntary. Adverse reac- children with aspirin intolerance, lactose-induced di- tions continue to be reported, although some are no arrhea, and propylene glycol-induced hyperosmola- longer considered clinically significant, and other new lity and lactic acidosis. Although many other excipi- reactions have emerged. The original statement, there- ents have been implicated in causing adverse fore, has been updated and its information expanded. reactions, these are the most significant in the pedi- atric population. ABBREVIATIONS. FDA, Food and Drug Administration; MDIs, metered-dose inhalers ANTIASTHMATIC MEDICATIONS It is readily appreciated that some percentage of asthmatic children will develop a “paradoxical” Pharmaceutical products often contain agents that bronchospasm after they inhale their medication. Be- have a variety of purposes, including improvement cause many of these reactions were attributed to of the appearance, bioavailability, stability, and pal- sulfite, which had been highly publicized as a caus- atability of the product. Excipients (substances ative agent, it was often first suspected. -
Sulfur Dioxide and Some Sulfites, Bisulfites and Metabisulfites
SULFUR DIOXIDE AND SOME SULFITES, BISULFITES AND METABISULFITES 1. Exposure Data 1.1 Chemical and physical data 1.1.1 Synonyms and structural and molecular data Sulfr dioxi Chem. Abstr. Serv Reg. No.: 7446-09-5 Replaced CAS Nos.: 8014-94-6; 12396-99-5; 83008-56-4; 89125-89-3 Chem. Abstr. Name; Sulfur dioxide IUPAC Systematic Name: Sulfur dioxide Synonyms: Sulfurous acid anhydride; sulfurous anhydride; sulfurous oxide; sulfur oxide (S02); sulfur superoxide; sulphur dioxide 0=8=0 S02 MoL. wt: 64.07 Sodium sulfte Chem. Abstr. Serv Reg. No.: 7757-83-7 Altemate CAS No.: 10579-83-6 Replaced CAS No.: 68135-69-3 Chem. Abstr. Name: Sulfurous acid, di sodium salt IUPAC Systematic Name: Sulfurous acid, disodium salt Synonyms: Anhydrous sodium sulfite; disodium sulfite; sodium sulphite o 1/ Na · 0 - 8 - 0 · Na Na2S0J MoL. wt: 126.04 Sodium bisulfe Chem. Abstr. Serv Reg. No.: 7631-90-5 Replaced CAS Nos.: 57414-01-4; 69098-86-8; 89830-27-3; 91829-63-9 Chem. Abstr. Name: Sulfurous acid, monosodium salt IUPAC Systematic Name: Sulfurous acid, monosodium salt -131- 132 lARe MONOGRAPHS VOLUME 54 Synonyms: Hydrogen sulfite sodium; monosodium sulfite; sodium acid sulfite; sodium bisulphite; sodium hydrogen sulfite; sodium sulfite (NaHS03) o Il HO - S - a · Na NaHS03 MoL. wt: 104.06 Sodium metabisulfte Chem. Abstr. Serv Reg. No.: 7681-57-4 Altemate CAS No.: 7757-74-6 Replaced CAS No.: 15771-29-6 Chem. Abstr. Name: Disulfurous acid, disodium salt IUPAC Systematic Name: Pyrosulfurous acid, disodium salt Synonyms: Disodium disulfite; disodium metabisulfite; disodium pyrosulfite; sodium disulfite; sodium metabisulphite; sodium pyrosulfite oIl Il0 Na · 0- S - a - S - a · Na .Na2S20S MoL. -
Synthetic and Biosynthetic Approaches to Cherylline and Related Compounds Richard Duane Shaffer Iowa State University
Iowa State University Capstones, Theses and Retrospective Theses and Dissertations Dissertations 1972 Synthetic and biosynthetic approaches to cherylline and related compounds Richard Duane Shaffer Iowa State University Follow this and additional works at: https://lib.dr.iastate.edu/rtd Part of the Organic Chemistry Commons Recommended Citation Shaffer, Richard Duane, "Synthetic and biosynthetic approaches to cherylline and related compounds " (1972). Retrospective Theses and Dissertations. 5277. https://lib.dr.iastate.edu/rtd/5277 This Dissertation is brought to you for free and open access by the Iowa State University Capstones, Theses and Dissertations at Iowa State University Digital Repository. It has been accepted for inclusion in Retrospective Theses and Dissertations by an authorized administrator of Iowa State University Digital Repository. For more information, please contact [email protected]. INFORMATION TO USERS This dissertation was produced from a microfilm copy of the original document. While the most advanced technological means to photograph and reproduce this document have been used, the quality is heavily dependent upon the quality of the original submitted. The following explanation of techniques is provided to help you understand markings or patterns which may appear on this reproduction. 1. The sign or "target" for pages apparently lacking from the document photographed is "Missing Page(s)". If it was possible to obtain the missing psge(s) or section, they are spliced into the film along with adjacent pages. This may have necessitated cutting thru an image and duplicating adjacent pages to insure you complete continuity. 2. When an image on the film is obliterated with a large round black mark, it is an indication that the photographer suspected that the copy may have moved during exposure and thus cause a blurred image. -
In Bisulfite/Permanganate for Organic Compounds Oxidation
Water Research 148 (2019) 198e207 Contents lists available at ScienceDirect Water Research journal homepage: www.elsevier.com/locate/watres New insight into the reactivity of Mn(III) in bisulfite/permanganate for organic compounds oxidation: The catalytic role of bisulfite and oxygen * Shifa Zhong, Huichun Zhang Department of Civil Engineering, Case Western Reserve University, 2104 Adelbert Road, Cleveland, OH, 44106-7201, USA article info abstract À À Article history: A recently discovered bisulfite(HSO3 )/permanganate(MnO4 ) system was reported to produce highly Received 24 June 2018 reactive free Mn(III) that can oxidize organic compounds in milliseconds. However, this characteristic Received in revised form reactivity was not found in all other known reaction systems that can also produce free Mn(III). Why can 18 September 2018 Mn(III) in NaHSO /KMnO be so active? Here, we found NaHSO and O acted as catalysts for the reaction Accepted 12 October 2018 3 4 3 2 between Mn(III) and organic compounds. Without O , 0% of organic compounds were oxidized in Available online 23 October 2018 2 NaHSO3/KMnO4, indicating the absence of O2 inactivated Mn(III) reactivity. When the reaction between NaHSO and KMnO was monitored in air, Mn(III) catalyzed rapid oxidation of NaHSO by O . Then, the Keywords: 3 4 3 2 Bisulfite and permanganate Mn(III) that could oxidize organic compounds was found to be the ones involved in the catalytic reaction Bisulfite/oxygen reaction between NaHSO3 and O2, thus the link between O2 and Mn(III) reactivity was established. Finally, Disproportionation NaHSO3/O2 can be viewed as catalysts for the reaction between Mn(III) and organic compounds because Mn(III) catalyst 1) when Mn(III) was involved in oxidizing organic compounds, it stopped being the catalyst for the Mn(III) oxidant reaction between NaHSO3 and O2 so that they were consumed to a much smaller extent; and 2) without Water treatment NaHSO3 and O2, Mn(III) lost its oxidation ability. -
Winemaking Basics-Bruce Hagen.Pdf
Winemaking Basics Bruce Hagen Sourcing grapes: good wine starts with good grapes Ripeness: is generally expressed as percent sugar or °Brix (°B). The normal range is 22 – 26°B (17.5 to 19 for sparkling and 21 for some ‘crisp’ and austere whites). Use a hydrometer or a refractometer to check it. If you harvest much above 26, you should consider diluting the juice (must) with water to adjust it to downward a bit, depending on the alcohol level you are comfortable with. The problem with making wines from high °Brix grapes is that the resulting alcohol level will be high. The fermentation may stop (stick) and the wine may taste hot. Therefore, you should consider diluting the must or juice, if the sugar level is much above 26 (see adjusting the °Brix below). The alcohol conversion factor for most yeasts is about .57, but ranges from .55 to as high as .64. Multiply the °B by the conversion factor to determine the probable alcohol level: ex 26°B x .57 = 14.8%. If the °B level is 27, the resulting alcohol level will be 15.4 —very hot! If you dilute to 25, the alcohol will be 14.25%. If you dilute it to 24ºB, the alcohol will be 13.7% —quite acceptable. Whites vs. reds: § White grapes are de-stemmed, crushed, and pressed before fermentation. § Skin contact is relatively short. § Red grapes are typically de-stemmed, crushed, cold-soaked (optional), and he wine pressed off the skins and seeds after fermentation. Skin contact is lengthy, so color and tannins are more intense. -
Website Exposure May Cause Bronchitis to Develop with Coughing, ( Or in Your Facility’S RTK Phlegm, And/Or Shortness of Breath
Right to Know Hazardous Substance Fact Sheet Common Name: SODIUM BISULFITE Synonym: Sodium Hydrogen Sulfite CAS Number: 7631-90-5 Chemical Name: Sulfurous Acid, Monosodium Salt RTK Substance Number: 1685 Date: August 1998 Revision: April 2008 DOT Number: UN 2693 (Solution) Description and Use EMERGENCY RESPONDERS >>>> SEE BACK PAGE Sodium Bisulfite is a white, crystalline solid with a slight odor Hazard Summary of rotten eggs. It is often in a liquid solution. It is used in Hazard Rating NJDOH NFPA making paper and leather, as a food preservative and in dye HEALTH 2 - and chemical production. FLAMMABILITY 0 - REACTIVITY 0 - CORROSIVE POISONOUS GASES ARE PRODUCED IN FIRE Reasons for Citation f Sodium Bisulfite is on the Right to Know Hazardous Substance List because it is cited by ACGIH, DOT, NIOSH, Hazard Rating Key: 0=minimal; 1=slight; 2=moderate; 3=serious; 4=severe IARC and EPA. f This chemical is on the Special Health Hazard Substance List. f Sodium Bisulfite can affect you when inhaled. f Contact can severely irritate and burn the skin and eyes. f Inhaling Sodium Bisulfite can irritate the nose, throat and lungs. f Sodium Bisulfite may cause a skin allergy and an asthma- like allergy. SEE GLOSSARY ON PAGE 5. f Sodium Bisulfite is CORROSIVE when in a liquid solution with water. FIRST AID Eye Contact f Quickly brush off excess chemical from the face. Immediately flush with large amounts of water for at least 60 Workplace Exposure Limits minutes, lifting upper and lower lids. Remove contact NIOSH: The recommended airborne exposure limit (REL) is lenses, if worn, while flushing. -
The Most Reactive Position of a 1,2,4-Triazine
1378 Vol. 35 (1987) Chem. Pharm. Bull. 35( 4 )1378-1382(1987) Studies on as-Triazine Derivatives. IX.1) Synthesis of 5-Substituted 1,2,4-Triazine Derivatives through an Addition Reaction and Subsequent Oxidation SHOETSU KONNO, SETSUYA OHBA, MATAICHI SAGI, and HIROSHI YAMANAKA* Pharmaceutical Institute, Tohoku University, Aobayama, Sendai 980, Japan (Received July 31, 1986) The addition reactions of various nucleophiles to 6-methyl-3-phenyl-1,2,4-triazine (1) were investigated and a practical preparation of 1 was developed. The reactions showed many similarities to those of quinazoline (at the 4-position) and acridine (at the 9-position). The hitherto unknown compounds 5-cyand- (3), 5-carbamoyl- (5) and 5-phenacy1-6-methyl-3-phenyl-1,2,4-triazines (11e) were synthesized. Keywords •\ 1,2,4-triazine; nucleophilic addition; aromatization; active methylene com- pound; catalytic reduction The most reactive position of a 1,2,4-triazine (as-triazine) ring is position 5, where nucleophiles can attack very easily.2) For example, 3,5,6-trichloro-as-triazine reacts with 1 mol eq of sodium methoxide to give 3,6-dichloro-5-methoxy-as-triazine exclusively.3) Further- more, the combined electron-attracting effects of three ring nitrogen atoms suggest posi- tion 5 to be highly susceptible to nucleophilic addition, when there is no leaving group at this position.4) The present paper deals with the synthesis of 5-substituted as-triazine derivatives from 6-methyl-3-phenyl-as-triazine (1). The reaction of 1 with nucleophiles came up to our expectation, as shown in Chart 1. Compound 1 reacted with sodium bisulfite in methanol to give 6-methy1-3-phenyl-2,5- dihydro-as-triazine-5-sulfonic acid (2). -
The Catalytic Hydrogenation of Benzodiazines
THE CATALYTIC HYDROGENATION OF BENZODIAZINES: I. PHTHALAZINE II. QUINAZOLINE A Dissertation Presented to the Department of Chemistry Brigha~ Young University In Partial Fulfillment of the Requirements for the Degre~ Doctor of Philosophy by Danny Lee Elder August 1969 This dissertation, by Danny Lee Elder, is accepted in its present form b y the Department of Chemistry of Brigham Young University as satisfying the dissertation requirement for the degree of Doctor of Philosophy. ii . , TO Lynette, David, and Douglas iii ACKNOWLEDGEMENTS Deep appreciation is expressed to Dr. H. Smith Broadbent, without whose friendly association, patient help, and kindly ex- · tended advice this research problem could not have been carried out. Gratitude is also expressed £or the many extra-academic endeavors Dr. Broadbent has made on my behalf. Appreciation is extended to the Department of Chemistry of Brigham Young University for financial support in the form of teaching and research assistantships. My wife deserves special thanks for her encouragement, patience, understanding, and especially, for making it all worth- while. Finally, sincere thanks go to a great group of fellow-graduate students--Craig Argyle, Weldon Burnham, Vic Mylroie, Wes Parish, and Walter Sudweeks--for helpful discussions, comrade- ship, and most of all, for the memorable hours spent at such places as Anderson Lake, Four-Lakes Basin, Klondike Bluff, and of course, "Organic Pass, 11 (Grosebeck Pass). iv TABLE OF CONTENTS Chapter Page I. INTRODUCTION • • • • • • • • • • • • • • • 1 II. LITERATURE REVIEW • • • • • • • • • • • • 4 Phthalaz~ne • • • • . 4 Structure and properties • • • • • • • • • · 4 Synthesis of phthalazine • • • • • • • • • 8 Reduced phthalazines • • • • • • • • • • 10 Quinazoline • • • • • • . 12 Structure and properties • . • 12 Synthesis of quinazoline • • • • • 15 Reduced quinazolines • • • • 18 Catalytic Hydrogenation of Benzoazines and Benzodiazines • • • • • • • • 20 Quinoline . -
Computer-Aided Identification, Synthesis, and Biological Evaluation of Novel Inhibitors for Botulinum Neurotoxin Serotype
BNL-108550-2015-JA Elsevier Editorial System(tm) for Bioorganic & Medicinal Chemistry Manuscript Draft Manuscript Number: Title: Computer-Aided Identification, Synthesis, and Biological Evaluation of Novel Inhibitors for Botulinum Neurotoxin Serotype Article Type: Full Length Article Keywords: Botulinum neurotoxin BoNT/A-LC inhibitor SNAPtide SNAP-25 HTP in silico screening Corresponding Author: Prof. Iwao Ojima, Ph.D. Corresponding Author's Institution: Stony Brook University First Author: Yu-Han G Teng, Ph.D. Order of Authors: Yu-Han G Teng, Ph.D.; William T Berger, Ph.D.; Natasha M Nesbitt, Ph.D.; Kunal Kumar, Ph.D.; Robert C Rizzo, Ph.D.; Peter J Tonge, Ph.D.; Iwao Ojima, Ph.D.; Subramanyam Swaminathan, Ph.D. Abstract: Botulinum neurotoxins (BoNTs) are among the most potent biological toxin known to humans, and are classified as Category A bioterrorism agents by the Centers for Disease Control and prevention (CDC). There are seven known BoNT serotypes (A-G) which have been thus far identified in literature. BoNTs have been shown to block neurotransmitter release by cleaving proteins of the soluble NSF attachment protein receptor (SNARE) complex. Disruption of the SNARE complex precludes motor neuron failure which ultimately results in flaccid paralysis in humans and animals. Currently, there are no effective therapeutic treatments against the neurotoxin light chain (LC) after translocation into the cytosols of motor neurons. In this work, high-throughput virtual screening was employed to screen a library of commercially available compounds from ZINC database against BoNT/A-LC. Among the hit compounds from the in-silico screening, two lead compounds were identified and found to have potent inhibitory activity against BoNT/A-LC in vitro, as well as in Neuro- 2a cells.