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1 the 2-Step Synthesis of Lidocaine Review
The 2-Step Synthesis of Lidocaine Review: You should review SN2 reactions. You also need to do some on your own reading of section 20- 15 in Wade. Make sure you are familiar with macroscale recrystallization and macroscale separation using a separatory funnel. Introduction: Lidocaine is a member of the Caine family of pharmaceutical local anesthetics. Figure 1 below shows the chemical structure of Lidocaine as well as three other members of this important family of numbing agents. Figure 1. Well-known compounds in the Caine family of local anesthetics NH2 H N CO2CH3 N CO2CH2CH3 N O O Ph N H N O O 2 O Lidocaine Cocaine Novocaine Benzocaine When used correctly, these compounds are very effective at providing local anesthesia, or the numbing feeling you get when you go to the dentist for a filling, for example. These compounds are administered topically, orally, or injected, depending on the situation. Topical creams and ointments that are available over the counter (OTC) generally contain Lidocaine and sometimes Benzocaine. Of the four compounds in Figure 1, Cocaine is not available OTC (hopefully this is obvious) and is not commonly used among the medical community due to its extremely addictive nature. Local anesthetics prevent us from experiencing pain in a small portion of the body, i.e., wherever it is applied. When a local anesthetic is injected directly into the spinal fluid, our entire lower body goes numb. An example of the latter is an epidural given to a woman in labor, most commonly Bupivacaine (structure not shown). A common example of a local anesthetic is the use of Benzocaine in teething gel (Orajel®) for infants. -
Assessment of Portable HAZMAT Sensors for First Responders
The author(s) shown below used Federal funds provided by the U.S. Department of Justice and prepared the following final report: Document Title: Assessment of Portable HAZMAT Sensors for First Responders Author(s): Chad Huffman, Ph.D., Lars Ericson, Ph.D. Document No.: 246708 Date Received: May 2014 Award Number: 2010-IJ-CX-K024 This report has not been published by the U.S. Department of Justice. To provide better customer service, NCJRS has made this Federally- funded grant report available electronically. Opinions or points of view expressed are those of the author(s) and do not necessarily reflect the official position or policies of the U.S. Department of Justice. Assessment of Portable HAZMAT Sensors for First Responders DOJ Office of Justice Programs National Institute of Justice Sensor, Surveillance, and Biometric Technologies (SSBT) Center of Excellence (CoE) March 1, 2012 Submitted by ManTech Advanced Systems International 1000 Technology Drive, Suite 3310 Fairmont, West Virginia 26554 Telephone: (304) 368-4120 Fax: (304) 366-8096 Dr. Chad Huffman, Senior Scientist Dr. Lars Ericson, Director UNCLASSIFIED This project was supported by Award No. 2010-IJ-CX-K024, awarded by the National Institute of Justice, Office of Justice Programs, U.S. Department of Justice. The opinions, findings, and conclusions or recommendations expressed in this publication are those of the author(s) and do not necessarily reflect those of the Department of Justice. This document is a research report submitted to the U.S. Department of Justice. This report has not been published by the Department. Opinions or points of view expressed are those of the author(s) and do not necessarily reflect the official position or policies of the U.S. -
Material Safety Data Sheet
Material Safety Data Sheet Chloroacetyl chloride, 98% ACC# 00956 Section 1 - Chemical Product and Company Identification MSDS Name: Chloroacetyl chloride, 98% Catalog Numbers: AC147290000, AC147290010, AC147290050, AC147291000, AC147292500 Synonyms: Chloracetyl chloride; Chloroacetic acid chloride. 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 79-04-9 Chloroacetyl chloride 98 201-171-6 Section 3 - Hazards Identification EMERGENCY OVERVIEW Appearance: colorless to light yellow liquid. Danger! Corrosive. Causes eye and skin burns. Causes digestive and respiratory tract burns. Harmful if swallowed, inhaled, or absorbed through the skin. Lachrymator (substance which increases the flow of tears). Moisture sensitive. Corrosive to metal. Target Organs: Lungs. Potential Health Effects Eye: Lachrymator (substance which increases the flow of tears). Causes eye irritation and burns. Skin: Harmful if absorbed through the skin. Causes severe skin irritation and burns. Ingestion: Harmful if swallowed. Causes gastrointestinal tract burns. Inhalation: Harmful if inhaled. Causes severe irritation of upper respiratory tract with coughing, burns, breathing difficulty, and possible coma. May cause abdominal pain, nausea, vomiting, and inflammation of the gums and mouth. Inhalation of high concentrations may cause pulmonary edema. Chronic: Prolonged or repeated exposure may cause lung irritation, chest pain, and pulmonary edema. 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. -
MSDS Butyl Acrylate
MATERIAL SAFETY DATA SHEET — Butyl Acrylate SECTION 1 — CHEMICAL PRODUCT AND COMPANY IDENTIFICATION Product Identifier [WHMIS Classification] Butyl Acrylate Product Use Manufacturer’s Name Supplier’s Name Ayers International Corp. Street Address Street Address P.O. Box 4312 City State City State Greenwich New York Postal Code Emergency Telephone Postal Code Emergency Telephone 06831 (800) 424 - 9300 Date MSDS Prepared MSDS Prepared By Phone Number 07/01/2010 J. Miller (203) 329 - 8919 SECTION 2 — COMPOSITION/INFORMATION ON INGREDIENTS Ingredients (specific) % CAS Number LD 50 of Ingredient LC 50 of Ingredient (specify (specify species and route species) Butyl Acrylate 99 141-32-2 Methyl Ether of Hydroquinone 10-20ppm 150-76-5 Hazardous Ingredients (specific) SECTION 3 — HAZARDS IDENTIFICATION Route of Entry Inhalation, Skin Absorption, Eye Contact, Skin Contact [Emergency Overview] WHMIS Symbols] Potential Health Effects Inhalation: Causes irritation of the respiratory tract, experienced as nasal discomfort and discharge, with chest pain, coughing, headache, nausea, vomiting, dizziness, drowsiness, disturbed vision and unconsciousness Eye Contact: Liquid or vapor causes irritation, experienced as stinging, excess blinking and tear production, with excess redness and swelling of the conjunctiva. Skin Contact: Causes irritation with discomfort, local redness, and possible swelling. Skin Absorption: Prolonged or widespread contact may result in the absorption of potentially harmful amounts of material. Swallowing: Slightly toxic. May cause abdominal discomfort, nausea, vomiting and diarrhea. May cause burning or painful sensations in the mouth, throat, chest, and abdomen. Aspiration into the lungs may occur during ingestion or vomiting, resulting in lung injury. Effects of Repeated Overexposure: Prolonged and repeated overexposure to butyl acrylate vapor may result in damage to the tissues of the nose and upper respiratory tract – an effect typically produced by irritant materials. -
Estimation of Hydrolysis Rate Constants of Carboxylic Acid Ester and Phosphate Ester Compounds in Aqueous Systems from Molecular Structure by SPARC
Estimation of Hydrolysis Rate Constants of Carboxylic Acid Ester and Phosphate Ester Compounds in Aqueous Systems from Molecular Structure by SPARC R E S E A R C H A N D D E V E L O P M E N T EPA/600/R-06/105 September 2006 Estimation of Hydrolysis Rate Constants of Carboxylic Acid Ester and Phosphate Ester Compounds in Aqueous Systems from Molecular Structure by SPARC By S. H. Hilal Ecosystems Research Division National Exposure Research Laboratory Athens, Georgia U.S. Environmental Protection Agency Office of Research and Development Washington, DC 20460 NOTICE The information in this document has been funded by the United States Environmental Protection Agency. It has been subjected to the Agency's peer and administrative review, and has been approved for publication. Mention of trade names of commercial products does not constitute endorsement or recommendation for use. ii ABSTRACT SPARC (SPARC Performs Automated Reasoning in Chemistry) chemical reactivity models were extended to calculate hydrolysis rate constants for carboxylic acid ester and phosphate ester compounds in aqueous non- aqueous and systems strictly from molecular structure. The energy differences between the initial state and the transition state for a molecule of interest are factored into internal and external mechanistic perturbation components. The internal perturbations quantify the interactions of the appended perturber (P) with the reaction center (C). These internal perturbations are factored into SPARC’s mechanistic components of electrostatic and resonance effects. External perturbations quantify the solute-solvent interactions (solvation energy) and are factored into H-bonding, field stabilization and steric effects. These models have been tested using 1471 reliable measured base, acid and general base-catalyzed carboxylic acid ester hydrolysis rate constants in water and in mixed solvent systems at different temperatures. -
GREEN BOOK 4 Alkyl Benzoates CIR EXPERT PANEL MEETING
GREEN BOOK 4 Alkyl Benzoates CIR EXPERT PANEL MEETING AUGUST 30-31, 2010 July 30, 2010 MEMORANDUM To: CIR Expert Panel and Liaisons From: Lillian C. Becker, M.S. Scientific Analyst and Writer Subject: Draft Report for C12-15 Alkyl Benzoate and related Alkyl Benzoates The Cosmetic Ingredient Review (CIR) announced the Scientific Literature Review (SLR) for alkyl benzoates in June, 2010. C12-15 alkyl benzoate is the lead ingredient of this safety assessment. Related alkyl benzoate ingredients are included. CIR has been informed that a comprehensive dossier on the C12-15 alkyl benzoates being prepared for the European REACH program will be completed and provided to CIR in late September or early October. The Panel should review the Draft Report and decide: 1) if it is reasonable to include the other listed ingredients with C12-15 alkyl benzoate in this report and 2) whether any additional data are needed in order to reach a safety conclusion for C12-15 alkyl benzoates and the related ingredients. If no additional data are required, then the Panel may issue a Tentative Report. Alternatively, the Panel may choose to table the report to await the receipt of the dossier mentioned above. CIR Panel Book Page 1 CIR Panel Book Page 2 History of Alkyl Benzoates June, 2010 – SLR issued. August, 2010 - CIR Panel Book Page 3 Search Strategy for Benzoates EXPORATORY SEARCH: PUBMED: “alkyl benzoate” – 7 hits, 1 useful; CAS No. – 0 hits. Internet (Dogpile) – “alkyl benzoate” ‐ 1 MSDS FULL SEARCH: PUBMED: “lauryl alcohol” – 53 hits, 6 ordered. Learned that Valerie was doing this ingredient. -
1. A. the First Reaction Is a Friedel-Crafts Acylation (FCA), Where the Major Product Is the Para- Isomer (60% Isolated Yield)
1. a. The first reaction is a Friedel-Crafts Acylation (FCA), where the major product is the para- isomer (60% isolated yield). The second reaction is a nitration, where the incoming electrophile (nitronium ion) is directed to the ortho position of the methoxy group. The last reaction is a Wolff-Kishner reduction that converts the acetyl group into an ethyl group. The nitro group does not react under these conditions. OCH OCH OCH OCH3 3 3 3 NO2 NO2 N2H4/KOH CH3COCl/AlCl3 H2SO4/HNO3 0 oC O CH 3 O CH3 CH3 (A) Reaction 1 (B) Reaction 2 (C) Reaction 3 (P) b. The best solvent for the FC-acylation is dichloromethane. Tetrahydrofuran is a fairly strong Lewis base, which would react and deactivate the AlCl3 catalyst. Ethanol would also react with AlCl3 and form alcoholates, which are inactive at FCA catalyst. Dichloromethane is polar enough to dissolve all three compounds but does not form adducts with AlCl3. Thus, aluminum chloride maintains its Lewis acidity. 3+ c. As discussed in lecture, AlCl3*6 H2O is not suitable as catalyst because the Al is not a strong Lewis acid anymore. In addition, larger amounts of water would destroy the acetyl chloride as well (=hydrolysis, CH3COCl + H2O ---- > CH3COOH + HCl). Consequently, the reaction would not proceed in the desired fashion. 3+ OH2 H2O OH2 Al H2O OH2 OH2 d. In order to determine the yield, one has to calculate the number of moles of the reactant and the product. nA = 1.90 mL * 0.996 g/mL/108.14 g/mol = 17.5 mmol nCH3COCl = 2.49 mL * 1.104 g/mL/78.5 g/mol = 35.0 mmol nAlCl3 = 4.67 g/133.5 g/mol = 35.0 mmol Compound (A) is the limiting reagent. -
United States Patent (19) (11) 4,129,595 Suzuki 45) Dec
United States Patent (19) (11) 4,129,595 Suzuki 45) Dec. 12, 1978 (54) PREPARATION OF CHLOROACETYL (56) References Cited CHLORDE PUBLICATIONS E. E. Blaise et al., Comptes Rendus (France), vol. 174, 75 Inventor: Shigeto Suzuki, San Francisco, Calif. pp. 1173-1174, (1922), (Chem. Abstr., vol. 16, 2480). 73) Assignee: Chevron Research Company, San Primary Examiner-Gerald A. Schwartz Francisco, Calif. Attorney, Agent, or Firm-D. A. Newell; John Stoner, Jr. (21) Appl. No.: 891,429 57 ABSTRACT Chloroacetyl chloride is prepared by reacting glycolic (22) Filed: Mar. 29, 1978 acid with thionyl chloride in the presence of nitrogen 51) int. C.’.............................................. CO7C 51/58 containing organic compound orphosphine compound. 52 U.S. C. ................................................ 260/544 Y 58 Field of Search .................................... 260/544 Y 3 Claims, No Drawings 4,129,595 1. 2 glycolic acid with thionyl chloride in the presence of a PREPARATION OF CHLOROACETYL CHLORDE catalytic amount of nitrogen-containing hydrocarbyl organic compound or hydrocarbyl phosphine com BACKGROUND OF THE INVENTION pound at high conversion and yield in accordance with 1. Field of the Invention 5 the present invention. The present invention relates to the preparation of chloroacetyl chloride. More particularly, the invention DETALED DESCRIPTION OF THE relates to the preparation of chloroacetyl chloride by INVENTION reacting glycolic acid with thionyl chloride in the pres The nitrogen-containing hydrocarbyl organic com ence of nitrogen-containing -
Ketene Reactions. I. the Addition of Acid Chlorides
KETENE REACTIONS. I. THE ADDITION OF ACID CHLORIDES TO DIMETHYLKETENE. II. THE CYCLOADDITION OF KETENES TO CARBONYL COMPOUNDS APPROVED: Graduate Committee: Major Professor Committee Member.rr^- Committee Member Committee Member Director of the Department of Chemistry Dean' of the Graduate School Smith, Larry, Ketene Reactions. I. The Addition of Acid Chlorides to DimethyIketene. II. The Cycloaddition of Ketenes to Carbonvl Compounds. Doctor of Philosophy (Chemistry), December, 1970, 63 pp., 3 tables, bibliography, 62 titles. Part I describes the addition of several acid chlorides to dimethylketene. The resulting 3-ketoacid chlorides were isolated and characterized. The reactivities of acid chlorides were found to parallel the parent acid pKa's. A reactivity order of ketenes toward acid chlorides was established. Dimethylketene is more reactive than ketene which is more reactive than diphenylketene. Attempts to effect the addition of an acid halide to a ketene produced by in situ dehydro- halogenation yielded a-halovinyl esters. The addition of acid chlorides to ketenes was concluded to be an ionic process dependent upon the nucleophilic character of the ketene oc- carbon and the polarity of the carbon-chlorine bond in the acid chloride. Part II describes the cycloaddition of several aldo- ketenes to chloral. The ketenes were generated in situ by dehydrohalogenation and dehalogenation of appropriately substituted acyl halides. Both cis- and trans-4-trichloro- Miyl-2-oxetanones are produced in the cycloadditions with the sterically hindered cis isomer predominating. Isomer distributions were determined by vpc or nmr analysis of the reaction solutions. Production of the ketenes by dehalo- genation resulted in enhanced reactivity of the carbonyl compounds. -
Study on Gas-Phase Mechanism of Chloroacetic Acid Synthesis by Catalysis and Chlorination of Acetic Acid
Asian Journal of Chemistry; Vol. 26, No. 2 (2014), 475-480 http://dx.doi.org/10.14233/ajchem.2014.15484 Study on Gas-Phase Mechanism of Chloroacetic Acid Synthesis by Catalysis and Chlorination of Acetic Acid * JIAN-WEI XUE , JIAN-PENG ZHANG, BO WU, FU-XIANG LI and ZHI-PING LV Research Institute of Special Chemicals, Taiyuan University of Technology, Taiyuan 030024, Shanxi Province, P.R. China *Corresponding author: Fax: +86 351 6111178; Tel: +86 351 60105503; E-mail: [email protected] Received: 14 March 2013; Accepted: 17 May 2013; Published online: 15 January 2014; AJC-14570 The process of acetic acid catalysis and chlorination for synthesizing chloroacetic acid can exist in not only gas phase but also liquid phase. In this paper, the gas-phase reaction mechanism of the synthesis of chloroacetic acid was studied. Due to the high concentration of acetic acid and the better reaction mass transfer in the liquid-phase reaction, the generation amount of the dichloroacetic acid was higher than that in the gas-phase reaction. Under the solution distillation, the concentration of acetyl chloride, whose boiling point is very low, was very high in the gas phase, sometimes even up to 99 %, which would cause the acetyl chloride to escape rapidly with the hydrogen chloride exhaust, so that the reaction slowed down. Therefore, series reactions occured easily in the gas-phase reaction causing the amount of the dichloroacetic acid to increase. Keywords: Gas phase, Catalysis, Chlorination, Chloroacetic acid, Acetic acid. INTRODUCTION Martikainen et al.3 summed up the reaction mechanism that was consistent with a mechanism found by Sioli according Chloroacetic acid is not only a fine chemical product but to the system condition experiment and systematic theoretical also an important intermediate in organic synthesis. -
Facile Synthesis and Polymerization of Ether Substituted Methacrylates
Polymer Journal, Vol. 27, No. 4, pp 325--338 (1995) Facile Synthesis and Polymerization of Ether Substituted Methacrylates Robert D. THOMPSON, Thomas B. BARCLAY, Kumar R. BASU, and Lon J. MATHIAS* Department of Polymer Science, University of Southern Mississippi, Hattiesburg, MS 39406-{)076, U.S.A. (Received May 12, 1994) ABSTRACT: New difunctional methacrylate monomers containing f3 heteroatoms have been synthesized from o:-hydroxymethylacrylate esters or o:-chloromethylacryloyl chloride. These monomers are more reactive than their alkane counterparts (e.g., ethacrylates), giving polymers with molecular weights comparable to poly(itaconate)s. The simple synthetic approach described allows a wide range of difunctionalized acrylate monomers to be produced. Variations in both ester and ether substituents were explored for ease of synthesis and polymerization. KEY WORDS Beta-Substituted Methacrylates / Disubstituted Ethylene / Functionalized Acrylates / Water-Soluble Acrylates / Poly(methacrylate)s / Ceiling Temperature/ Chain Transfer/ Acrylate monomers containing hydrocarbon alkyl ix-hydroxymethylacrylates8 with yields chains at the ex-position, such as the ethyl and ranging up to approximately 50% of readily propyl derivatives (1 and 2, Figure 1), display purified monomer. Reaction of the hydroxy very poor or no free radical polymerizability methyl group with appropriate reagents gives at room temperature. 1 Incorporation of an reactive ally! halides 7 •9 •10 capable of high oxygen atom fJ to the double bond (as in 3) yield conversion to a range of derivatives makes monomers which are much more reac (Figure 2). The ether's flexibility imparts tive. For example, the methyl ester of the ex unique properties to the monomer compared hydroxymethyl compound polymerizes faster to similar, more rigid ester derivatives; for than methyl methacrylate in free radical poly example, the ally! ether of ethyl ix-hydroxy merization, 2 although ether derivatives give methylacrylate undergoes efficient cyclopo molecular weights only up to ca. -
Development of Chemoinformatic Tools to Enumerate Functional Groups in Molecules for Organic Aerosol Characterization G
Manuscript prepared for Atmos. Chem. Phys. with version 2015/04/24 7.83 Copernicus papers of the LATEX class copernicus.cls. Date: 1 March 2016 Technical Note: Development of chemoinformatic tools to enumerate functional groups in molecules for organic aerosol characterization G. Ruggeri1 and S. Takahama1 1ENAC/IIE Swiss Federal Institute of Technology Lausanne (EPFL), Lausanne, Switzerland Correspondence to: Satoshi Takahama (satoshi.takahama@epfl.ch) Abstract. Functional groups (FGs) can be used as a reduced representation of organic aerosol composition in both ambient and environmental controlled chamber studies, as they retain a cer- tain chemical specificity. Furthermore, FG composition has been informative for source apportion- ment, and various models based on a group contribution framework have been developed to calcu- 5 late physicochemical properties of organic compounds. In this work, we provide a set of validated chemoinformatic patterns that correspond to: 1) a complete set of functional groups that can entirely describe the molecules comprised in the α-pinene and 1,3,5-trimethylbenzene MCMv3.2 oxidation schemes, 2) FGs that are measurable by Fourier transform infrared spectroscopy (FTIR), 3) groups incorporated in the SIMPOL.1 vapor pressure estimation model, and 4) bonds necessary for the cal- 10 culation of carbon oxidation state. We also provide example applications for this set of patterns. We compare available aerosol composition reported by chemical speciation measurements and FTIR for different emission sources, and calculate the FG contribution to the O:C ratio of simulated gas phase composition generated from α-pinene photooxidation (using MCMv3.2 oxidation scheme). 1 Introduction 15 Atmospheric aerosols are complex mixtures of inorganic salts, mineral dust, sea salt, black carbon, metals, organic compounds, and water (Seinfeld and Pandis, 2006).