DOCSLIB.ORG

1230 Date: May 1999 Revision: February 2009 DOT Number: UN 2938

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
1230 Date: May 1999 Revision: February 2009 DOT Number: UN 2938 Right to Know Hazardous Substance Fact Sheet Common Name: METHYL BENZOATE Synonyms: Methyl Benzenecarboxylate; Niobe Oil CAS Number: 93-58-3 Chemical Name: Benzoic Acid, Methyl Ester RTK Substance Number: 1230 Date: May 1999 Revision: February 2009 DOT Number: UN 2938 Description and Use EMERGENCY RESPONDERS >>>> SEE LAST PAGE Methyl Benzoate is a colorless, oily liquid with a pleasant, Hazard Summary fruity odor. It is used in perfumes and as a solvent. Hazard Rating NJDOH NFPA HEALTH - 1 FLAMMABILITY - 2 REACTIVITY - 0 COMBUSTIBLE POISONOUS GASES ARE PRODUCED IN FIRE Hazard Rating Key: 0=minimal; 1=slight; 2=moderate; 3=serious; Reasons for Citation 4=severe f Methyl Benzoate is on the Right to Know Hazardous Substance List because it is cited by DOT and NFPA. f Methyl Benzoate can affect you when inhaled and may be absorbed through the skin. f Contact can irritate the skin and eyes. f Inhaling Methyl Benzoate can irritate the nose, throat and lungs. f Methyl Benzoate may cause a skin allergy and an asthma- like allergy. f Repeated exposure to high levels may affect the nervous SEE GLOSSARY ON PAGE 5. system. FIRST AID Eye Contact Workplace Exposure Limits f Immediately flush with large amounts of water for at least 15 No occupational exposure limits have been established for minutes, lifting upper and lower lids. Remove contact lenses, if worn, while rinsing. Methyl Benzoate. However, it may pose a health risk. Always follow safe work practices. Skin Contact f Quickly remove contaminated clothing. Immediately wash f It should be recognized that Methyl Benzoate can be contaminated skin with large amounts of soap and water. absorbed through your skin, thereby increasing your exposure. Inhalation f Remove the person from exposure. f Begin rescue breathing (using universal precautions) if breathing has stopped and CPR if heart action has stopped. f Transfer promptly to a medical facility. EMERGENCY NUMBERS Poison Control: 1-800-222-1222 CHEMTREC: 1-800-424-9300 NJDEP Hotline: 1-877-927-6337 National Response Center: 1-800-424-8802 METHYL BENZOATE Page 2 of 6 Determining Your Exposure Reproductive Hazard f According to the information presently available to the New f Read the product manufacturer’s Material Safety Data Jersey Department of Health, Methyl Benzoate has not Sheet (MSDS) and the label to determine product been tested for its ability to affect reproduction. ingredients and important safety and health information about the product mixture. Other Effects f Methyl Benzoate may cause a skin allergy. If allergy f For each individual hazardous ingredient, read the New develops, very low future exposure can cause itching and a Jersey Department of Health Hazardous Substance Fact skin rash. Sheet, available on the RTK website f Methyl Benzoate may cause an asthma-like allergy. Future (www.nj.gov/health/eoh/rtkweb) or in your facility’s RTK exposure can cause asthma attacks with shortness of Central File or Hazard Communication Standard file. breath, wheezing, coughing, and/or chest tightness. f Repeated exposure to high levels may affect the nervous f You have a right to this information under the New Jersey system. Worker and Community Right to Know Act, the Public Employees Occupational Safety and Health (PEOSH) Act if you are a public worker in New Jersey, and under the federal Occupational Safety and Health Act (OSHA) if you Medical are a private worker. Medical Testing If symptoms develop or overexposure is suspected, the f The New Jersey Right to Know Act requires most following are recommended: employers to label chemicals in the workplace and requires public employers to provide their employees with f Lung function tests. The results may be normal if the person information concerning chemical hazards and controls. is not having an attack at the time of the test. The federal OSHA Hazard Communication Standard (29 f Evaluation by a qualified allergist can help diagnose skin CFR 1910.1200) and the PEOSH Hazard Communication allergy. f Exam of the nervous system Standard (N.J.A.C. 12:100-7) require employers to provide similar information and training to their employees. Any evaluation should include a careful history of past and present symptoms with an exam. Medical tests that look for This Fact Sheet is a summary of available information damage already done are not a substitute for controlling regarding the health hazards that may result from exposure. exposure. Duration of exposure, concentration of the substance and other factors will affect your susceptibility to any of the potential Request copies of your medical testing. You have a legal right effects described below. to this information under the OSHA Access to Employee Exposure and Medical Records Standard (29 CFR 1910.1020). Health Hazard Information Mixed Exposures Acute Health Effects f Smoking can cause heart disease, lung cancer, The following acute (short-term) health effects may occur emphysema, and other respiratory problems. It may worsen immediately or shortly after exposure to Methyl Benzoate: respiratory conditions caused by chemical exposure. Even if you have smoked for a long time, stopping now will reduce f Contact can irritate the skin and eyes. your risk of developing health problems. f Inhaling Methyl Benzoate can irritate the nose, throat and lungs causing coughing, wheezing and/or shortness of breath. Chronic Health Effects The following chronic (long-term) health effects can occur at some time after exposure to Methyl Benzoate and can last for months or years: Cancer Hazard f According to the information presently available to the New Jersey Department of Health, Methyl Benzoate has not been tested for its ability to cause cancer in animals. METHYL BENZOATE Page 3 of 6 Workplace Controls and Practices Eye Protection Very toxic chemicals, or those that are reproductive hazards or f Wear indirect-vent, impact and splash resistant goggles sensitizers, require expert advice on control measures if a less when working with liquids. toxic chemical cannot be substituted. Control measures f If additional protection is needed for the entire face, use in include: (1) enclosing chemical processes for severely combination with a face shield. A face shield should not be irritating and corrosive chemicals, (2) using local exhaust used without another type of eye protection. ventilation for chemicals that may be harmful with a single exposure, and (3) using general ventilation to control Respiratory Protection exposures to skin and eye irritants. For further information on Improper use of respirators is dangerous. Respirators workplace controls, consult the NIOSH document on Control should only be used if the employer has implemented a written Banding at www.cdc.gov/niosh/topics/ctrlbanding/. program that takes into account workplace conditions, requirements for worker training, respirator fit testing, and The following work practices are also recommended: medical exams, as described in the OSHA Respiratory f Label process containers. Protection Standard (29 CFR 1910.134). f Provide employees with hazard information and training. f Monitor airborne chemical concentrations. f At any detectable concentration, use a NIOSH approved full f Use engineering controls if concentrations exceed facepiece respirator with an organic vapor cartridge. recommended exposure levels. Increased protection is obtained from full facepiece f Provide eye wash fountains and emergency showers. powered-air purifying respirators. f Wash or shower if skin comes in contact with a hazardous f Leave the area immediately if (1) while wearing a filter or material. cartridge respirator you can smell, taste, or otherwise detect f Always wash at the end of the workshift. Methyl Benzoate, (2) while wearing particulate filters f Change into clean clothing if clothing becomes abnormal resistance to breathing is experienced, or (3) eye contaminated. irritation occurs while wearing a full facepiece respirator. f Do not take contaminated clothing home. Check to make sure the respirator-to-face seal is still good. f Get special training to wash contaminated clothing. If it is, replace the filter or cartridge. If the seal is no longer f Do not eat, smoke, or drink in areas where chemicals are good, you may need a new respirator. being handled, processed or stored. f Consider all potential sources of exposure in your workplace. f Wash hands carefully before eating, smoking, drinking, You may need a combination of filters, prefilters or cartridges applying cosmetics or using the toilet. to protect against different forms of a chemical (such as vapor and mist) or against a mixture of chemicals. f Where the potential for high exposure exists, use a NIOSH approved supplied-air respirator with a full facepiece Personal Protective Equipment operated in a pressure-demand or other positive-pressure The OSHA Personal Protective Equipment Standard (29 CFR mode. For increased protection use in combination with an auxiliary self-contained breathing apparatus operated in a 1910.132) requires employers to determine the appropriate pressure-demand or other positive-pressure mode. personal protective equipment for each hazard and to train employees on how and when to use protective equipment. The following recommendations are only guidelines and may Fire Hazards If employees are expected to fight fires, they must be trained not apply to every situation. and equipped as stated in the OSHA Fire Brigades Standard (29 CFR 1910.156). Gloves and Clothing f Avoid skin contact with Methyl Benzoate. Wear personal f Methyl Benzoate is a COMBUSTIBLE LIQUID. protective equipment made from material which can not be f Use dry chemical, CO2 or foam as extinguishing agents. permeated or degraded by this substance. Safety f Water spray may be used to blanket fire. DO NOT USE equipment suppliers and manufacturers can provide solid water jets. recommendations on the most protective glove and clothing f POISONOUS GASES ARE PRODUCED IN FIRE. material for your operation. f Use water spray to keep fire-exposed containers cool.
Load more

Recommended publications
  • Retention Indices for Frequently Reported Compounds of Plant Essential Oils
    Retention Indices for Frequently Reported Compounds of Plant Essential Oils V. I. Babushok,a) P. J. Linstrom, and I. G. Zenkevichb) National Institute of Standards and Technology, Gaithersburg, Maryland 20899, USA (Received 1 August 2011; accepted 27 September 2011; published online 29 November 2011) Gas chromatographic retention indices were evaluated for 505 frequently reported plant essential oil components using a large retention index database. Retention data are presented for three types of commonly used stationary phases: dimethyl silicone (nonpolar), dimethyl sili- cone with 5% phenyl groups (slightly polar), and polyethylene glycol (polar) stationary phases. The evaluations are based on the treatment of multiple measurements with the number of data records ranging from about 5 to 800 per compound. Data analysis was limited to temperature programmed conditions. The data reported include the average and median values of retention index with standard deviations and confidence intervals. VC 2011 by the U.S. Secretary of Commerce on behalf of the United States. All rights reserved. [doi:10.1063/1.3653552] Key words: essential oils; gas chromatography; Kova´ts indices; linear indices; retention indices; identification; flavor; olfaction. CONTENTS 1. Introduction The practical applications of plant essential oils are very 1. Introduction................................ 1 diverse. They are used for the production of food, drugs, per- fumes, aromatherapy, and many other applications.1–4 The 2. Retention Indices ........................... 2 need for identification of essential oil components ranges 3. Retention Data Presentation and Discussion . 2 from product quality control to basic research. The identifi- 4. Summary.................................. 45 cation of unknown compounds remains a complex problem, in spite of great progress made in analytical techniques over 5.
    [Show full text]
  • Zn-Nx Sites on N-Doped Carbon for Aerobic Oxidative Cleavage
    ARTICLE https://doi.org/10.1038/s41467-021-25118-0 OPEN Zn-Nx sites on N-doped carbon for aerobic oxidative cleavage and esterification of C(CO)-C bonds ✉ ✉ Chao Xie1, Longfei Lin 2, Liang Huang 3, Zixin Wang1, Zhiwei Jiang 1, Zehui Zhang1 & Buxing Han 2 Selective cleavage of C-C bonds is very important in organic chemistry, but remains chal- lenging because of their inert chemical nature. Herein, we report that Zn/NC-X catalysts, in 1234567890():,; which Zn2+ coordinate with N species on microporous N-doped carbon (NC) and X denotes the pyrolysis temperature, can effectively catalyze aerobic oxidative cleavage of C(CO)-C bonds and quantitatively convert acetophenone to methyl benzoate with a yield of 99% at 100 °C. The Zn/NC-950 can be applied for a wide scope of acetophenone derivatives as well as more challenging alkyl ketones. Detail mechanistic investigations reveal that the catalytic performance of Zn/NC-950 can be attributed to the coordination between Zn2+ and N species to change the electronic state of the metal, synergetic effect of the Zn single sites with their surrounding N atoms, as well as the microporous structure with the high surface area and structural defects of the NC. 1 Key Laboratory of Catalysis and Energy Materials Chemistry of Ministry of Education & Hubei Key Laboratory of Catalysis and Materials Science, South- Central University for Nationalities, Wuhan, China. 2 Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Colloid, Interface and Chemical Thermodynamics, Institute of Chemistry, Chinese Academy of Sciences, Beijing, China. 3 The State Key Laboratory of Refractories and Metallurgy, ✉ Wuhan University of Science and Technology, Wuhan, China.
    [Show full text]
  • Working with Hazardous Chemicals
    A Publication of Reliable Methods for the Preparation of Organic Compounds Working with Hazardous Chemicals The procedures in Organic Syntheses are intended for use only by persons with proper training in experimental organic chemistry. All hazardous materials should be handled using the standard procedures for work with chemicals described in references such as "Prudent Practices in the Laboratory" (The National Academies Press, Washington, D.C., 2011; the full text can be accessed free of charge at http://www.nap.edu/catalog.php?record_id=12654). All chemical waste should be disposed of in accordance with local regulations. For general guidelines for the management of chemical waste, see Chapter 8 of Prudent Practices. In some articles in Organic Syntheses, chemical-specific hazards are highlighted in red “Caution Notes” within a procedure. It is important to recognize that the absence of a caution note does not imply that no significant hazards are associated with the chemicals involved in that procedure. Prior to performing a reaction, a thorough risk assessment should be carried out that includes a review of the potential hazards associated with each chemical and experimental operation on the scale that is planned for the procedure. Guidelines for carrying out a risk assessment and for analyzing the hazards associated with chemicals can be found in Chapter 4 of Prudent Practices. The procedures described in Organic Syntheses are provided as published and are conducted at one's own risk. Organic Syntheses, Inc., its Editors, and its Board of Directors do not warrant or guarantee the safety of individuals using these procedures and hereby disclaim any liability for any injuries or damages claimed to have resulted from or related in any way to the procedures herein.
    [Show full text]
  • Covalent Bonding - Benzoic Acid from Ethyl Benzoate by Base Hydrolysis C1031 Expt 2
    Covalent Bonding - Benzoic Acid from Ethyl Benzoate by Base Hydrolysis C1031 Expt 2 EXPERIMENT 2: Covalent Bonding - Benzoic Acid from Ethyl Benzoate by Base Hydrolysis Introduction Ethyl benzoate (boiling point 211-213°C, melting point -34°C) belongs to a class of compounds called esters. It is a sweet smelling, colourless, liquid used in perfumery under the name Essence de Niobe; in the manufacture of Peau d’Espagne; and as an artificial fruit essence. It is soluble in organic solvents but insoluble in water. When ethyl benzoate is shaken with water two liquid layers form. The upper layer is ethyl benzoate (less dense) and the lower layer is water. There is no clear indication of any reaction taking place. A more careful study shows that ethyl benzoate reacts very slowly with water and is hydrolyzed1 to give benzoic acid and ethanol but the reaction does not go to completion. However, ethyl benzoate is found to react much faster with aqueous sodium hydroxide, the reaction going to completion, to give sodium benzoate (water soluble) and ethanol (miscible with water). - + O O CH2 CH3 O O Na (aq) C C + NaOH(aq) + CH3 CH2 OH Reaction 1 ethyl benzoate aqueous sodium hydroxide sodium benzoate ethanol (C9H10O2) (C7H5O2Na) This process is called base hydrolysis (or saponification) of an ester and is used in this experiment to first obtain sodium benzoate solution, and then benzoic acid from ethyl benzoate. The ethanol may be recovered by simple downward distillation from the reaction mixture and collected as a solution in water. But this step is omitted in this experiment to allow it to be completed in the available time.
    [Show full text]
  • Effect of Reaction Time on Base Hydrolysis of Methyl Benzoate
    EFFECT OF REACTION TIME ON BASE HYDROLYSIS OF METHYL BENZOATE ROSSIDAH SINJAANAK DAVID DARI (43864) Bachelor ofScience with Honours (Resource Chemistry) 2016 EFFECT OF REACTIONN TIME ON BASE HYDROLYSIS OF METHYL BENZOATE ROSSIDAH SINJA ANAK DAVID DARI (43864) This project paper is submitted in partial fulfillment of requirements the Degree of Bachelor of Science with honors (Program of Resource Chemistry) Faculty of Resource Science and Technology UNIVERSITI MALAYSIA SARAWAK 2016 II ,...... 7 r Acknowledgement I would like to express my deepest gratitude to the many people that helped to bring this research project to success. I want to thank, first and foremost my supervisor, Miss Yusralina bt Yusof for providing me the opportunity to taking part in this Final Year Project. I am so grateful for her help, professionalism and valuable guidance throughout this project that I do not have enough words to give my sincere appreciation. I would also like to thank all the staffs that involve in the analysis of data for this research project. Without their passionate participation and input, the analysis of data could not have successfully conducted. I am indebted to my friends who support me in this research project through the entire year. I cannot find words to express my gratitude to them in making this research project to fruition. I consider it an honor to work with all of them during this project. Last but not least, I must express my profound gratitude to my parents for providing me with unfailing support throughout my years of study and through the process of researching and writing this thesis.
    [Show full text]
  • Recommended Methods for the Identification and Analysis of Cocaine in Seized Materials
    Recommended methods for the Identification and Analysis of Cocaine in Seized Materials MANUAL FOR USE BY NATIONAL DRUG ANALYSIS LABORATORIES Photo credits: UNODC Photo Library; UNODC/Ioulia Kondratovitch; Alessandro Scotti. Laboratory and Scientific Section UNITED NATIONS OFFICE ON DRUGS AND CRIME Vienna Recommended Methods for the Identification and Analysis of Cocaine in Seized Materials (Revised and updated) MANUAL FOR USE BY NATIONAL DRUG ANALYSIS LABORATORIES UNITED NATIONS New York, 2012 Note Operating and experimental conditions are reproduced from the original reference materials, including unpublished methods, validated and used in selected national laboratories as per the list of references. A number of alternative conditions and substitution of named commercial products may provide comparable results in many cases, but any modification has to be validated before it is integrated into laboratory routines. Mention of names of firms and commercial products does not imply the endorse- ment of the United Nations. ST/NAR/7/REV.1 Original language: English © United Nations, March 2012. All rights reserved. The designations employed and the presentation of material in this publication do not imply the expression of any opinion whatsoever on the part of the Secretariat of the United Nations concerning the legal status of any country, territory, city or area, or of its authorities, or concerning the delimitation of its frontiers or boundaries. This publication has not been formally edited. Publishing production: English, Publishing and Library Section, United Nations Office at Vienna. ii Contents Page 1. Introduction ................................................. 1 1.1 Background .............................................. 1 1.2 Purpose and use of the manual .............................. 1 2. Physical appearance and chemical characteristics of coca leaf and illicit materials containing cocaine ................................
    [Show full text]
  • 045 of the Ethyl Ether of ?It;;, Yellow Monoclinic Prisms, Showing a Great Tentleiicy to Form Twins and Twin Clusters
    I'KEPAKA'I'ION 01.' ES'I'GKS BY KEPLi\CEBIEXT OP BLKOXYL. 045 of the ethyl ether of ?it;;, yellow monoclinic prisms, showing a great tentleiicy to form twins and twin clusters. If any condensation product (m.p., 216') is formed it may be removed by dissolving the ethoxy com- pound in ether. The pure ether melts at 133". '1 he crystals of this ether were examined by Mr. Walter B. Jones of the Geology Department and his report is as follows : photomicrograph X-l!; ocular, 2; objective, 3; arc light; exposure 3 seconds through blue &i\s and through 12 mm. of solution. Triclinic system, tabular habit; lxiul, macro and brachy pinacoids, usually modified by unit prism, 1na~~10:rnd hrachy domes. Inclination of angle, --So * . Subs, 0.3872. AgCl, 0.8013. Calc. for CIOHIIO~N&!I~:C1, 33.80. Found 33.70 Ethers of the Higher Alcohols.--So ethers could be made with n- prop?*1,u-butyl and iso-amyl alcohols although both methods of prepara- tion were tried a number of times, and inodifications of these methods were rcwrted to. Summary. hen ethers are obtained by the action of alcohols upon the addition products of chloral and wazefa- or prim-nitro-aniline. The vi-nitro-aniline product gave ethers with methyl, ethyl, wpropyl, n-butyl and iso-amyl alcohols. The p-nitro-aniline product gaye ethers only with methyl and ethyl alcohols. In these cases the amine was made to react with the chloral alcoholate. No ethers of the higher alcohols could be obtained. ('l14PT:L HILL,N.
    [Show full text]
  • Experiment 5 Carboxylic Acids and Saponification of Methyl Benzoate
    Experiment 5 Carboxylic Acids and Saponification of Methyl Benzoate In the first part of this experiment you are going to evaluate the solubility of salicylic acid in water, hot water and in the presence of aqueous NaOH. As you would expect carboxylic acids should react with water to form a water soluble carboxylate anion but solubility is also dependent of the size of the alkyl or aryl group attached to the carboxylic acid functional group. In general the following acid-base reaction occurs: - + R-COOH + H2O RCOO (aq) + H3O (aq) The structure for salicylic acid is given below: OH C OH O Salicylic acid Additionally, carboxylic acids react with bases to form water soluble salts as shown below: - + R-COOH + NaOH (aq) RCOO Na (aq) + H2O Note that salicylic acid contains, in addition to the carboxylic acid functional group, a phenol group hydrogen that can also be titrated by base. The resultant sodium carboxylate/phenolate salt can further react with acids to reform the free acid (COOH) and phenol (Ph-OH) as shown below: R-COO-Na+ (aq) + HCl (aq) RCOOH + NaCl (aq) Ph-O-Na+ (aq) + HCl (aq) Ph-OH + NaCl (aq) The use of bases and acids serves as solubility switches to convert an insoluble form of a compound to a soluble form and vice versa. Observing the solubility or insolubility of reactants and/or products serves as a means to monitor acid base reactions. The concept of a solubility switch will also serve as the basis for following the base (NaOH) catalyzed hydrolysis (saponification) reaction of an ester (methyl benzoate) to the subsequent water soluble carboxylate salt (sodium benzoate) and alcohol (methanol).
    [Show full text]
  • Methyl Benzoate
    CHM230 - Preparation of Methyl Benzoate Preparation of Methyl Benzoate Introduction The ester group is an important functional group that can be synthesized in a number of different ways. The low-molecular-weight esters have very pleasant odors and indeed are the major components of the flavor and odor aspects of a number of fruits. Although the natural flavor may contain nearly a hundred different compounds, single esters approximate the natural odors and are often used in the food industry for artificial flavors and fragrances. Esters can be prepared by the reaction of a carboxylic acid with an alcohol in the presence of a catalyst such as concentrated sulfuric acid, hydrogen chloride, p-toluenesulfonic acid, or the acid form of an ion exchange resin: This Fischer esterification reaction reaches equilibrium after a few hours of refluxing. The position of the equilibrium can be shifted by adding more of the acid or of the alcohol, depending on cost or availability. The mechanism of the reaction involves initial protonation of the carboxyl group, attack by the nucleophilic hydroxyl, a proton transfer, and loss of water followed by loss of the catalyzing proton to give the ester. In this experiment you will prepare methyl benzoate by reacting benzoic acid with methanol using sulfuric acid as a catalyst. Since this is a reversible reaction, it will reach an equilibrium that is described by the equilibrium constant, Keq . For this experiment, you will isolate the product, methyl benzoate, and any unreacted benzoic acid. Using this data, you will calculate the equilibrium constant for the reaction (see calculation section below).
    [Show full text]
  • Dielectric Constant Chart
    Dielectric Constants of Common Materials DIELECTRIC MATERIALS DEG. F CONSTANT ABS RESIN, LUMP 2.4-4.1 ABS RESIN, PELLET 1.5-2.5 ACENAPHTHENE 70 3 ACETAL 70 3.6 ACETAL BROMIDE 16.5 ACETAL DOXIME 68 3.4 ACETALDEHYDE 41 21.8 ACETAMIDE 68 4 ACETAMIDE 180 59 ACETAMIDE 41 ACETANILIDE 71 2.9 ACETIC ACID 68 6.2 ACETIC ACID (36 DEGREES F) 36 4.1 ACETIC ANHYDRIDE 66 21 ACETONE 77 20.7 ACETONE 127 17.7 ACETONE 32 1.0159 ACETONITRILE 70 37.5 ACETOPHENONE 75 17.3 ACETOXIME 24 3 ACETYL ACETONE 68 23.1 ACETYL BROMIDE 68 16.5 ACETYL CHLORIDE 68 15.8 ACETYLE ACETONE 68 25 ACETYLENE 32 1.0217 ACETYLMETHYL HEXYL KETONE 66 27.9 ACRYLIC RESIN 2.7 - 4.5 ACTEAL 21 3.6 ACTETAMIDE 4 AIR 1 AIR (DRY) 68 1.000536 ALCOHOL, INDUSTRIAL 16-31 ALKYD RESIN 3.5-5 ALLYL ALCOHOL 58 22 ALLYL BROMIDE 66 7 ALLYL CHLORIDE 68 8.2 ALLYL IODIDE 66 6.1 ALLYL ISOTHIOCYANATE 64 17.2 ALLYL RESIN (CAST) 3.6 - 4.5 ALUMINA 9.3-11.5 ALUMINA 4.5 ALUMINA CHINA 3.1-3.9 ALUMINUM BROMIDE 212 3.4 ALUMINUM FLUORIDE 2.2 ALUMINUM HYDROXIDE 2.2 ALUMINUM OLEATE 68 2.4 1 Dielectric Constants of Common Materials DIELECTRIC MATERIALS DEG. F CONSTANT ALUMINUM PHOSPHATE 6 ALUMINUM POWDER 1.6-1.8 AMBER 2.8-2.9 AMINOALKYD RESIN 3.9-4.2 AMMONIA -74 25 AMMONIA -30 22 AMMONIA 40 18.9 AMMONIA 69 16.5 AMMONIA (GAS?) 32 1.0072 AMMONIUM BROMIDE 7.2 AMMONIUM CHLORIDE 7 AMYL ACETATE 68 5 AMYL ALCOHOL -180 35.5 AMYL ALCOHOL 68 15.8 AMYL ALCOHOL 140 11.2 AMYL BENZOATE 68 5.1 AMYL BROMIDE 50 6.3 AMYL CHLORIDE 52 6.6 AMYL ETHER 60 3.1 AMYL FORMATE 66 5.7 AMYL IODIDE 62 6.9 AMYL NITRATE 62 9.1 AMYL THIOCYANATE 68 17.4 AMYLAMINE 72 4.6 AMYLENE 70 2 AMYLENE BROMIDE 58 5.6 AMYLENETETRARARBOXYLATE 66 4.4 AMYLMERCAPTAN 68 4.7 ANILINE 32 7.8 ANILINE 68 7.3 ANILINE 212 5.5 ANILINE FORMALDEHYDE RESIN 3.5 - 3.6 ANILINE RESIN 3.4-3.8 ANISALDEHYDE 68 15.8 ANISALDOXINE 145 9.2 ANISOLE 68 4.3 ANITMONY TRICHLORIDE 5.3 ANTIMONY PENTACHLORIDE 68 3.2 ANTIMONY TRIBROMIDE 212 20.9 ANTIMONY TRICHLORIDE 166 33 ANTIMONY TRICHLORIDE 5.3 ANTIMONY TRICODIDE 347 13.9 APATITE 7.4 2 Dielectric Constants of Common Materials DIELECTRIC MATERIALS DEG.
    [Show full text]
  • Supporting Information
    Supporting information Oxidative cleavage of α-arylaldehydes using iodosylbenzene Nizam Havare and Dietmar A. Plattner S1 General: All used substrate were prepared following published procedures [a-m]. Starting materials: (diacetoxyiodo)benzene, Dess-Martin reagent, 2-(4-nitrophenyl)ethanol, 2-(4- chlorophenyl)ethanol, phenylacetaldehyde, 2-(2-naphthyl)ethanol, 2-(4-methoxy)ethanol, 2- methoxy-2-phenylethanol, 2-phenylpropanal, 2-phenyl-1-butanol, cyclohexyl- phenylacetonitrile, α-tetralone, 2-acetylnaphthalene, anethol, 4-nitroacetophenone and solvents were obtained commercially from ABCR , Sigma-Aldrich , Fluka , Alfa Aesar and Acros. Dichloromethane was dried over potassium carbonate, freshly distilled and stored under Ar prior to use. Cyclohexane was dried over sodium, freshly distilled and stored under Ar prior to use. Ethyl acetate was dried over phosphor pentaoxide, freshly distilled and stored under Ar prior to use. Column chromatography: Silica gel 60 : 0.06-0.2 mm, Carl Roth GmbH. 1 TLC: Silica gel 60 F 254 25 Aluminium sheets 20x20 cm from Merck KGaA co. Darmstadt. H- spectra: Varian 300 and Bruker 500 spectrometer. GC-MS: (GC Varian 3400 , achiral GC column Macherey-Nagel optima 5 MS 30 m x0.25 mmØ, 0.25 µm film). MS: Thermo TSQ 700. Preparation of CO detection reagent (PdCl 2/HCl): 100 ml of water is added to 130 mg of palladium(II)chloride (0.733 mmol, 99.7%) in a 250 ml volumetric flask. 1 ml of HCl solution is added, which was prepared from mixture of conc. HCl/water (V/V = 1:10). The suspension is stirred for one day at room temperature, until giving a clear solution.
    [Show full text]
  • United States Patent [191 [11] 3,943,181 Fleischer Et Al
    United States Patent [191 [11] 3,943,181 Fleischer et al. , [45] Mar. 9, 1976 [54] SEPARATING OPTICALLY PURE d- AND 397,212 8/1933 United Kingdom ........... .. 260/631 R l-ISOMERS 0F MENTHOL, NEOMENTHOL AND ISOMENTHOL " OTHER PUBLICATIONS [75] Inventors: Jiirgen Fleischer, Cologne; Kurt Gilman Ed., Organic Chemistry, Wiley, N.Y., 1943, p. Bauer; Ruldolf Hopp, both of 254. Holzminden, all of Germany Reed et al_, J. Chem. Soc., pp. 167-173 (1933). [73] Assignee: Haarmann & Reimer Gesellschaft mit beschrankter Haftung Primary Examiner-Be1‘nard l-lel?n Assistant Examiner-James H. Reamer [22] Filed: Sept. 3, 1974 Attorney, Agent, or Firm—Burgess, Dinklage & [21] Appl. No.: 503,004 Sprung Related US. Application Data [63] Continuation of Ser. No. 229,109, Feb. 24, 1972, [57] ABSTRACT ' abandoned. A process for the separation of optically active d— and [30] Foreign Application Priority Data l-isomers of a compound selected from the group con sisting of menthol, neomenthol and isomenthol, which Feb. 27, 1971 Germany .......................... .. 2109456 comprises esterifying a d,l-isomeric mixture of the Feb. 2, 1972 Germany .......................... .. 2204771 compound with an acid selected from the group con sisting of benzoic acid optionally carrying at least one [52] US. Cl...... 260/631 R; 260/473 R; 260/471 R; substituent on the benzene ring and hexahydrobenzoic 260/468 R; 260/476 R acid; forming a supersaturated solution or a super [51] Int. Cl.2 ........................................ .. C07C 35/12 cooled melt of the dJ-ester; inoculating the solution or [58] Field of Search ................... .. 260/631 R, 631 H melt with crystals of the d- or l-form of the ester to effect selective crystallization of one of the two [56] References Cited optical isomers; separating the crystals and subjecting UNITED STATES PATENTS them to hydrolysis to yield the corresponding enantio 2,120,131 6/1938 Harris ..........................
    [Show full text]