Methanol Safety During the COVID-19 Pandemic
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SAFETY DATA SHEET Isopropyl Alcohol
SAFETY DATA SHEET Isopropyl Alcohol Section 1. Identification GHS product identifier : Isopropyl Alcohol Chemical name : Isopropyl alcohol Other means of : isopropanol; 2-Propanol identification Product type : Liquid. Product use : Synthetic/Analytical chemistry. Synonym : isopropanol; 2-Propanol SDS # : 001105 Supplier's details : Airgas USA, LLC and its affiliates 259 North Radnor-Chester Road Suite 100 Radnor, PA 19087-5283 1-610-687-5253 24-hour telephone : 1-866-734-3438 Section 2. Hazards identification OSHA/HCS status : This material is considered hazardous by the OSHA Hazard Communication Standard (29 CFR 1910.1200). Classification of the : FLAMMABLE LIQUIDS - Category 2 substance or mixture EYE IRRITATION - Category 2A SPECIFIC TARGET ORGAN TOXICITY (SINGLE EXPOSURE) (Narcotic effects) - Category 3 GHS label elements Hazard pictograms : Signal word : Danger Hazard statements : May form explosive mixtures with air. Highly flammable liquid and vapor. Causes serious eye irritation. May cause drowsiness or dizziness. Precautionary statements General : Read label before use. Keep out of reach of children. If medical advice is needed, have product container or label at hand. Prevention : Wear protective gloves. Wear eye or face protection. Keep away from heat, hot surfaces, sparks, open flames and other ignition sources. No smoking. Use explosion- proof electrical, ventilating, lighting and all material-handling equipment. Use only non- sparking tools. Take precautionary measures against static discharge. Keep container tightly closed. Use only outdoors or in a well-ventilated area. Avoid breathing vapor. Wash hands thoroughly after handling. Response : IF INHALED: Remove person to fresh air and keep comfortable for breathing. Call a POISON CENTER or physician if you feel unwell. -
N-BUTYL ALCOHOL
Right to Know Hazardous Substance Fact Sheet Common Name: n-BUTYL ALCOHOL Synonyms: Propyl Carbinol; n-Butanol CAS Number: 71-36-3 Chemical Name: 1-Butanol RTK Substance Number: 1330 Date: November 1998 Revision: January 2008 DOT Number: UN 1120 Description and Use EMERGENCY RESPONDERS >>>> SEE BACK PAGE n-Butyl Alcohol is a colorless liquid with a strong, sweet Hazard Summary alcohol odor. It is used as a solvent for fats, waxes, shellacs, Hazard Rating NJDOH NFPA resins, gums, and varnish, in making hydraulic fluids, and in HEALTH - 2 medications for animals. FLAMMABILITY - 3 REACTIVITY - 0 f ODOR THRESHOLD = 1 to 15 ppm FLAMMABLE f Odor thresholds vary greatly. Do not rely on odor alone to POISONOUS GASES ARE PRODUCED IN FIRE determine potentially hazardous exposures. CONTAINERS MAY EXPLODE IN FIRE Hazard Rating Key: 0=minimal; 1=slight; 2=moderate; 3=serious; Reasons for Citation 4=severe f n-Butyl Alcohol is on the Right to Know Hazardous f n-Butyl Alcohol can affect you when inhaled and by Substance List because it is cited by OSHA, ACGIH, DOT, passing through the skin. NIOSH, DEP, IRIS, NFPA and EPA. f Contact can irritate and burn the skin. f This chemical is on the Special Health Hazard Substance f n-Butyl Alcohol can irritate and burn the eyes with possible List. eye damage. f Inhaling n-Butyl Alcohol can irritate the nose, throat and lungs. f Exposure to n-Butyl Alcohol can cause headache, dizziness, nausea and vomiting. SEE GLOSSARY ON PAGE 5. f n-Butyl Alcohol can damage the liver, kidneys, hearing, and sense of balance. -
Williamson Ether Synthesis the Williamson Ether Synthesis Is an Organic Reaction, Forming an Ether from an Alkyl Halide and an Alcohol
The Williamson ether synthesis The Williamson ether synthesis is an organic reaction, forming an ether from an alkyl halide and an alcohol. This reaction was developed by Alexander Williamson in 1850. It involves the reaction of an alkoxide ion with a primary alkyl halide via an SN2 reaction. The Williamson reaction is widely used in both laboratory and industrial synthesis, and remains the simplest and most popular method of preparing ethers. Both symmetrical and asymmetrical ethers are easily prepared. The reaction for this week: an example of a Williamson ether synthesis acetaminophen ethyl iodide phenacetin starting material reagent product Phenacetin may be synthesized as an example of the Williamson ether synthesis The first synthesis of phenacetin was reported in 1878 by Harmon Morse. Procedure 1. Weigh an Extra-Strength Tylenol tablet. Pulverize the tablet with mortar and pestle. Weigh out 0.22 g and place it in a dry 15-ml round-bottom flask along with 0.28 g of finely pulverized K2CO3 (mortar and pestle) and 3.0 mL of butanone. Carefully add 0.28 mL of ethyl iodide with a syringe. 2. Add a stir bar; attach a microscale water-cooled condenser to the flask. Heat the mixture under reflux directly on a hot plate at medium setting for 1 hour. In the meantime, obtain the IR of acetaminophen. 3. Turn off the heat. Allow the mixture to cool down. Add 4 mL of water to the flask and transfer its contents to a 16 x 125 mm test tube with a screw cap. Rinse round-bottom flask 4 times with 1 mL of tert-butyl methyl ether (BME) and add the rinsings to the test tube. -
How Is Alcohol Metabolized by the Body?
Overview: How Is Alcohol Metabolized by the Body? Samir Zakhari, Ph.D. Alcohol is eliminated from the body by various metabolic mechanisms. The primary enzymes involved are aldehyde dehydrogenase (ALDH), alcohol dehydrogenase (ADH), cytochrome P450 (CYP2E1), and catalase. Variations in the genes for these enzymes have been found to influence alcohol consumption, alcohol-related tissue damage, and alcohol dependence. The consequences of alcohol metabolism include oxygen deficits (i.e., hypoxia) in the liver; interaction between alcohol metabolism byproducts and other cell components, resulting in the formation of harmful compounds (i.e., adducts); formation of highly reactive oxygen-containing molecules (i.e., reactive oxygen species [ROS]) that can damage other cell components; changes in the ratio of NADH to NAD+ (i.e., the cell’s redox state); tissue damage; fetal damage; impairment of other metabolic processes; cancer; and medication interactions. Several issues related to alcohol metabolism require further research. KEY WORDS: Ethanol-to acetaldehyde metabolism; alcohol dehydrogenase (ADH); aldehyde dehydrogenase (ALDH); acetaldehyde; acetate; cytochrome P450 2E1 (CYP2E1); catalase; reactive oxygen species (ROS); blood alcohol concentration (BAC); liver; stomach; brain; fetal alcohol effects; genetics and heredity; ethnic group; hypoxia The alcohol elimination rate varies state of liver cells. Chronic alcohol con- he effects of alcohol (i.e., ethanol) widely (i.e., three-fold) among individ- sumption and alcohol metabolism are on various tissues depend on its uals and is influenced by factors such as strongly linked to several pathological concentration in the blood T chronic alcohol consumption, diet, age, consequences and tissue damage. (blood alcohol concentration [BAC]) smoking, and time of day (Bennion and Understanding the balance of alcohol’s over time. -
Phosphine-Catalyzed Additions of Nucleophiles and Electrophiles to Α
PHOSPHINE-CATALYZED ADDITIONS OF NUCLEOPHILES AND ELECTROPHILES TO α,β–UNSATURATED CARBONYL COMPOUNDS Reported by Michael Scott Bultman November 4, 2004 INTRODUCTION Organophosphorous compounds are becoming increasingly important in organic synthesis. Phosphines serve as precursors to phosphonium ylides in the Wittig reaction,1 and as nucleophilic triggers in the Mitsunobu2 and Staudinger3 reactions. In these processes, the phosphine is stoichiometrically consumed and converted into a phosphine oxide. Phosphines are also commonly used as ligands for transition metal-catalyzed reactions, to modulate reactivity and stereocontrol.4 On the other hand, the use of phosphines as nucleophilic catalysts for organic reactions has only gained attention in the last ten years. First reported by Rauhut and Currier in 1963,5 phosphine catalysis has since been reinvestigated after the phosphine ligands in some transition-metal-catalyzed reactions were found to be better catalysts than the metal/phosphine complexes alone!6 Phosphines are well suited for catalyzing the addition of both nucleophiles and electrophiles to electron deficient alkenes, alkynes, and allenes. Activation of these α,β-unsaturated carbonyl systems with the phosphine enables the formation of new bonds at the α-, β-, and γ-positions. This report will highlight these different modes of addition to α,β-unsaturated carbonyl systems under phosphine catalysis that allow for the formation of a wide array of products from a single class of substrates. GENERAL REACTIVITY OF PHOSPHINES Key characteristics required for successful nucleophilic catalysis lie in the balance of leaving group ability, nucleophilicity, and ease of ylid formation. Increasing leaving group ability can often be + correlated with decreasing basicity. -
Alcohols I 1400
ALCOHOLS I 1400 Table 1 MW: Table 1 CAS: Table 2 RTECS: Table 2 METHOD: 1400, Issue 2 EVALUATION: PARTIAL Issue 1: 15 February 1984 Issue 2: 15 August 1994 OSHA : Table 2 PROPERTIES: Table 1 NIOSH: Table 2 ACGIH: Table 2 COMPOUNDS AND SYNONYMS: (1) ethanol: ethyl alcohol. (2) isopropyl alcohol: 2-propanol. (3) tert-butyl alcohol: 2-methyl-2-propanol. SAMPLING MEASUREMENT SAMPLER: SOLID SORBENT TUBE TECHNIQUE: GAS CHROMATOGRAPHY, FID (coconut shell charcoal, 100 mg/50 mg) ANALYTE: compounds above FLOW RATE: 0.01 to 0.2 L/min (£0.05 L/min for ethyl alcohol) DESORPTION: 1 mL 1% 2-butanol in CS 2 (1) (2) (3) INJECTION VOL-MIN: 0.1 L 0.3 L 1.0 L VOLUME: 5 µL -MAX: 1 L 3 L 10 L TEMPERATURE-INJECTION: 200 °C SHIPMENT: cooled -DETECTOR: 250-300 °C -COLUMN: 65-70 °C SAMPLE STABILITY: unknown, store in freezer CARRIER GAS: N2 or He, 30 mL/min BLANKS: 2 to 10 field blanks per set COLUMN: glass, 2 m x 4-mm ID, 0.2% Carbowax 1500 on 60/80 Carbopack C or equivalent ACCURACY CALIBRATION: solutions of analyte in eluent (internal standard optional) RANGE STUDIED: see EVALUATION OF METHOD RANGE AND BIAS: not significant [1] PRECISION: see EVALUATION OF METHOD OVERALL PRECISION (S ˆ ): see EVALUATION OF METHOD rT ESTIMATED LOD: 0.01 mg per sample [2] ACCURACY: ± 14% APPLICABILITY: The working ranges are 16 to 1000 ppm ethanol (30 to 1900 mg/m 3) for a 1-L air sample; 4 to 400 ppm isopropyl alcohol (10 to 1000 mg/m 3) for a 3-L air sample; and 1 to 100 ppm t-butyl alcohol (3 to 300 mg/m 3) for a 10-L air sample. -
Process Design and Simulation of Propylene and Methanol Production Through Direct and Indirect Biomass Gasification by Bernardo
Process Design and Simulation of Propylene and Methanol Production through Direct and Indirect Biomass Gasification by Bernardo Rangel Lousada A dissertation submitted to the graduate faculty of Auburn University in partial fulfillment of the requirements for the degree of Master in Chemical Engineering Auburn, Alabama August 6, 2016 Keywords: Process Design, Gasification, Biomass, Propylene, Methanol, Aspen Plus, Simulation, Economic, Synthesis Copyright 2016 by Bernardo Lousada Approved by Mario R. Eden, Chair and McMillan Professor of Chemical Engineering Allan E. David, John W. Brown Assistant Professor Professor of Chemical Engineering Selen Cremaschi, B. Redd Associate Professor Professor of Chemical Engineering Abstract As a result of increasing environmental concerns and the depletion of petroleum resources, the search for renewable alternatives is an important global topic. Methanol produced from biomass could be an important intermediate for liquid transportation fuels and value-added chemicals. In this work, the production of methanol and propylene is investigated via process simulation in Aspen Plus. Two gasification routes, namely, direct gasification and indirect gasification, are used for syngas production. The tar produced in the process is converted via catalytic steam reforming. After cleanup and treatment, the syngas is converted to methanol which will be further converted to high value olefins such as ethylene, propylene and butene via the methanol to propylene (MTP) processes. For a given feedstock type and supply/availability, we compare the economics of different conversion routes. A discounted cash flow with 10% of internet rate of return along 20 years of operation is done to calculate the minimum selling price of propylene required which is used as the main indicator of which route is more economic attractive. -
Methanol:Acetone Fixation and PGL-1 Staining Protocol
MeOH/Acetone fixation and staining of C. elegans for anti-PGL-1 whole-mount staining adapted by Erik Andersen from Mello Lab protocol by Daryl Conte, February, 2006 Things you will need: Micro Slides, precleaned, frosted, 25 x 75 mm (VWR cat no. 48312-002) Micro cover glasses, 25 mm square (VWR cat no. 48366-067) Micro cover glasses, 18 mm square (VWR cat no. 48366-045) PAP pen Polylysine (Sigma) Coplin jars Block/wedge of dry ice in Styrofoam box with lid – dry ice must be flat as slides will be placed on top 100% Methanol (-20°C in Coplin jar) 100% Acetone (-20°C in Coplin jar) Humid chamber – a plastic lidded box with moistened paper towels or whatmann paper in the bottom and a support to hold slides above paper Gravid adult worms or Larvae grown at 23ºC for at least two generations Mounting medium with antifade DAPI or other counterstain Glass Depression slide Water in which to wash larvae 20 μL pipet and mouth-pipette tubing Coating slides with polylysine – do this the day before. Many slides can be coated and stored for future use. 1. Prepare 0.01% polylysine solution. 2. Pipette polylysine solution (about 10 μL) onto surface of slide. 3. Dry slides thoroughly at 65°C. I dry them overnight. 4. It seems best to label your slides with a diamond pen, because later alcohol-fixation steps dissolve most inks. Fixing larvae to slides 1. Transfer >100 larvae of the same stage to 100 μL of water in a glass depression slide. It is very important to pick animals of the same stage, as larger worms, detritus or embryos will not allow for good crushing and subsequent fixation. -
Safety Data Sheet
SAFETY DATA SHEET Flammable Liquefied Gas Mixture: Ethanol / Isobutanol / Isopropanol (Isopropyl Alcohol) / Methanol / N-Butane / N-Butanol (N-Butyl Alcohol) / N-Propanol / Sec-Butyl Alcohol (2-Butanol) / Tert Butanol Section 1. Identification GHS product identifier : Flammable Liquefied Gas Mixture: Ethanol / Isobutanol / Isopropanol (Isopropyl Alcohol) / Methanol / N-Butane / N-Butanol (N-Butyl Alcohol) / N-Propanol / Sec-Butyl Alcohol (2-Butanol) / Tert Butanol Other means of : Not available. identification Product use : Synthetic/Analytical chemistry. SDS # : 011439 Supplier's details : Airgas USA, LLC and its affiliates 259 North Radnor-Chester Road Suite 100 Radnor, PA 19087-5283 1-610-687-5253 Emergency telephone : 1-866-734-3438 number (with hours of operation) Section 2. Hazards identification OSHA/HCS status : This material is considered hazardous by the OSHA Hazard Communication Standard (29 CFR 1910.1200). Classification of the : FLAMMABLE GASES - Category 1 substance or mixture GASES UNDER PRESSURE - Liquefied gas GHS label elements Hazard pictograms : Signal word : Danger Hazard statements : Extremely flammable gas. Contains gas under pressure; may explode if heated. May cause frostbite. May form explosive mixtures in Air. May displace oxygen and cause rapid suffocation. Precautionary statements General : Read and follow all Safety Data Sheets (SDS’S) before use. Read label before use. Keep out of reach of children. If medical advice is needed, have product container or label at hand. Close valve after each use and when empty. Use equipment rated for cylinder pressure. Do not open valve until connected to equipment prepared for use. Use a back flow preventative device in the piping. Use only equipment of compatible materials of construction. -
Hand Sanitizers and Updates on Methanol Testing
Hand Sanitizers and Updates on Methanol Testing Francis Godwin Director, Office of Manufacturing Quality, Office of Compliance Center for Drug Evaluation and Research, FDA USP Global Seminar Series: Ensuring Quality Hand Sanitizer Production During Covid-19 for Manufacturers February 23, 2021 • DISCLAIMER: The views and opinions expressed in this presentation are those of the authors and do not necessarily represent official policy or positions of the Food & Drug Administration www.fda.gov 2 Outline ● What OMQ Does ● General Background on Hand Sanitizer ● Recent Safety Concerns and FDA Actions ● Substitution ● Methanol Testing Requirements for Drug Product Manufacturers www.fda.gov 3 Office of Manufacturing Quality What We Do 4 CDER/OC Mission To shield patients from poor- quality, unsafe, and ineffective drugs through proactive compliance strategies and risk-based enforcement action. www.fda.gov 5 What OMQ Does • We evaluate compliance with Current Good Manufacturing Practice (CGMP) for drugs based on inspection reports and evidence gathered by FDA investigators. • We develop and implement compliance policy and take regulatory actions to protect the public from adulterated drugs in the U.S. market. Source: FDA www.fda.gov 6 Drug Adulteration Provisions U.S. Federal Food, Drug, & Cosmetic Act • 501(a)(2)(A): Insanitary conditions • 501(a)(2)(B): Failure to conform with CGMP • 501(b): Strength, quality, or purity differing from official compendium • 501(c): Misrepresentation of strength, etc., where drug is unrecognized in compendium • 501(d): Mixture with or substitution of another substance • 501(j): Deemed adulterated if owner/operator delays, denies, refuses, or limits inspection www.fda.gov 7 CGMP Legal Authority Section 501(a)(2)(B) requires conformity with CGMP A drug is adulterated if the methods, facilities, or controls used in its manufacture, processing, packing, or holding do not conform to CGMP to assure that such drug meets purported characteristics for safety, identity, strength, quality, and purity. -
In Vitro Nitric Oxide Scavenging Activity of Methanol Extracts of Three Bangladeshi Medicinal Plants
ISSN: 2277- 7695 CODEN Code: PIHNBQ ZDB-Number: 2663038-2 IC Journal No: 7725 Vol. 1 No. 12 2013 Online Available at www.thepharmajournal.com THE PHARMA INNOVATION - JOURNAL In Vitro Nitric Oxide Scavenging Activity Of Methanol Extracts Of Three Bangladeshi Medicinal Plants Rozina Parul1*, Sukalayan Kumar Kundu 2 and Pijush Saha2 1. Department of Pharmacy, Gono Bishwabidyalay, Savar, Dhaka – 1344, Bangladesh. E-mail: [email protected] 2. Department of Pharmacy, Jahangirnagar University, Savar, Dhaka – 1342, Bangladesh. The methanol extracts of three medicinal plants named Phyllunthus freternus, Triumfetta rhomboidae and Casuarina littorea were examined for their possible regulatory effect on nitric oxide (NO) levels using sodium nitroprusside as a NO donor in vitro. Most of the extracts tested demonstrated direct scavenging of NO and exihibited significant activity and the potency of scavenging activity was in the following order: Phyllunthus freternus > Leaves of Triumfetta rhomboidae > Casuarina littorea > barks of Triumfetta rhomboidae > roots of Triumfetta rhomboidae. All the evaluated extracts exhibited a dose dependent NO scavenging activity. The methanolic extracts of Phyllunthus freternus showed the greatest NO scavenging effect of 60.80% at 200 µg/ml with IC50 values 48.27 µg/ml as compared to the positive control ascorbic acid where 96.27% scavenging was observed at similar concentration with IC50 value of 5.47 µg/ml. The maximum NO scavenging of Leaves of Triumfetta rhomboidae, barks of Triumfetta rhomboidae, roots of Triumfetta rhomboidae and Casuarina littorea were 53.94%, 50.43%, 33.23% and 54.02% with IC50 values 97.81 µg/ml, 196.89 µg/ml, > 200 µg/ml and 168.17 µg/ml respectively. -
And Isopropyl Alcohol for Methanol, Including During the Public Health Emergency (COVID-19)
Contains Nonbinding Recommendations Policy for Testing of Alcohol (Ethanol) and Isopropyl Alcohol for Methanol, Including During the Public Health Emergency (COVID-19) Guidance for Industry January 2021 U.S. Department of Health and Human Services Food and Drug Administration Center for Drug Evaluation and Research (CDER) Center for Biologics Evaluation and Research (CBER) Center for Veterinary Medicine (CVM) Current Good Manufacturing Practice (CGMP) Contains Nonbinding Recommendations Preface Public Comment This guidance is being issued to address the Coronavirus Disease 2019 (COVID-19) public health emergency. This guidance is being implemented without prior public comment because the Food and Drug Administration (FDA or the Agency) has determined that prior public participation for this guidance is not feasible or appropriate (see section 701(h)(1)(C) of the Federal Food, Drug, and Cosmetic Act (FD&C Act) and 21 CFR 10.115(g)(2)). This guidance document is being implemented immediately, but it remains subject to comment in accordance with the Agency’s good guidance practices. Comments may be submitted at any time for Agency consideration. Submit written comments to the Dockets Management Staff (HFA-305), Food and Drug Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852. Submit electronic comments to https://www.regulations.gov. All comments should be identified with the docket number FDA-2020-D-2016 and complete title of the guidance in the request. Additional Copies Additional copies are available from the FDA webpage