Kindle 9,95 € 9,95 € Sofort lieferbar. Oder 1,26 €, um das MP3-Album zu kaufen Toluene. It is an aromatic hydrocarbon that is widely used as an industrial feedstock and as a solvent. NIOSH REL: 100 ppm (375 mg/m 3) TWA, 150 ppm (560 mg/m 3) STEL. The following resources provide information about occupational exposure to toluene. The level of exposure depends upon the dose, duration, and work being done. Found in nature in a type of balsam tree called the tolu balsam, as well as in crude oil; toluene is also present in the environment as a result of its use as an additive in such products as nail polish, cigarettes, gasoline, dyes, perfume, explosives, paints and thinners, adhesives, and other manufactured goods. Both sources provide toluene for commercial use, but larger amounts are made by catalytic r Centers for Disease Control and Prevention. Exposure to toluene can result in temporary effects such as headaches, dizziness and cracked skin, as well as more serious effects such as reproductive damage and respiratory complications. Benzene: The molar mass of benzene is about 78.11 g/mol. Allergies and immunotoxicity: Ingredients linked to harm to the immune system, a class of health problems that manifest as allergic reactions or an impaired capacity to fight disease and repair damaged tissue in the body. This is seen among people working in may different occupations. Toluene is a clear, colorless liquid which becomes a vapor when exposed to air at room temperature. 4000, NIOSH Immediately Dangerous to Life or Health Concentrations (IDLH): Toluene, NIOSH Worker Notification Program: Shoe Manufacturers, Agency for Toxic Substances and Disease Registry (ATSDR): ToxFAQs™ for Toluene, ATSDR’s Medical Management Guidelines: Toluene, EPA Acute Exposure Guideline Levels: Toluene, EPA Consumer Fact Sheet Ground and Drinking Water: Toluene, EPA Integrated Risk Information System: Toluene, NLM Hazardous Substance Data Bank: Toluene, NLM (Household Products Database): Toluene, Canadian Centre for Occupational Health and Safety: Toluene, OECD Global Portal to Information on Chemical Substances: Toluene, WHO (Environmental Health Criteria 52): Toluene, National Institute for Occupational Safety and Health, U.S. Department of Health & Human Services, Workers in locations where there are leaking underground gasoline storage tanks, Construction workers who use paint, adhesives or solvents, Workers involved with the production of gasoline. 1-3, p. 578) reports that the lethal doses of toluene and benzene in mice are 10,000 and 14,000 ppm, respectively. Aromatics, Benzene, Toluene & Xylene (B2B Procurement) United Kingdom Summary: 2020 Economic Crisis Impact on Revenues & Financials (English Edition) von United Kingdom Editorial DataGroup | 23. 2549), NIOSH PUB: Toluene Diffusive sampler, No. 2,4-Diaminotoluene, precursor to toluene diisocyanate and azo dye. Toluene is an aromatic hydrocarbon consisting of a CH 3 group attached to a phenyl ring. As such, its IUPAC systematic name is methylbenzene. Explosions have been reported [NFPA 491M 1991]. What is toluene. What is the WHMIS 1988 classification? It comprises 15–20 percent of coal-tar light oil and is a minor constituent of petroleum. 58 / Monday, March 26, 2012 / Rules and Regulations Date of issue: 03/21/2014 Revision date: 02/27/2018 Supersedes: 03/21/2014 Version: 1.1 02/27/2018 EN (English) Page 1 SECTION 1: Identification . As an inhalant, toluene is known to have euphoric and dissociative effects. Toluene can remain unchanged for a long time in soil or water that is not in contact with air. To a 250 ml conical flask, N-acetylglycine (0.177 g, 1 mmol) was suspended in toluene (5.3 ml), heated the solution and stirred until it was clear and then a solution of isocyanate or diisocyanate (0.16 ml, 1 mmol) in chloroform (5.7 ml) was added drop wise and refluxed for 2 hrs after addition of 3-4 drops of triethylamine and then cooled to room temperature (25 AdegC). Toluene is on the Proposition 65 list because it can cause birth defects or other reproductive harm.Significant exposure to toluene during pregnancy may affect the baby’s development. Toluene is used in many industries. The key difference between benzene and toluene is their structure; toluene has a methyl group attached to the benzene ring while benzene has no methyl groups attached.. Benzene and Toluene are two aromatic compounds having a slight difference between them in their structure. Another correct answer is that toluene is an aromatic compound. Saving Lives, Protecting People, New Jersey Hazardous Substance Fact Sheets: Toluene, The National Institute for Occupational Safety and Health (NIOSH), Managing Chemical Safety in the Workplace, NMAN: S-Benzylmercapturic acid and S-phenylmercapturic acid in urine 8326, NIOSH Criteria for a Recommended Standard: Occupational Exposure to Toluene, NIOSH Occupational Health Guideline for Toluene, NIOSH Volatile Organic CPDS (Screening) (No. Learn more about exposure limits here. Provides links and references to additional resources related to exposures to toluene. Toluene: Toluene is an organic compound having a benzene ring attached to a methyl group. Exposure to toluene can cause eye and nose irritation, tiredness, confusion, euphoria, dizziness, headache, dilated pupils, tears, anxiety, muscle fatigue, insomnia, nerve damage, inflammation of the skin, and liver and kidney damage. These types of exposures may make workers sick immediately or cause effects over time. Toluene (methyl benzene) is a chemical that is widely used in various substances within the home such as glue, paint and paint removers, and polish. More information about the health hazards of toluene is available here. Workers using toluene-containing paints, varnishes, shellac, nail polish, glues and adhesives, rust preventives or printing inks may be exposed to toluene. It is a good solvent (a substance that can dissolve other substances). Reaction with water liberates carbon dioxide. Toluene diisocyanate unspecified isomers (Benzene, 1,3-diisocyanatomethyl-, CASRN 26471-62-5) Q5. Recreational use: Toluene, in the manner of recreational use, is used as an intoxicative inhalant. Toluene is a liquid chemical compound utilized in the manufacturing of many commercial products, including paints and glues. It can also be referred as methylbenzene, anisen, and phenyl methane. Incompatible with strong oxidizing agents. Toluene is typically used in a mixture with other solvents and chemicals such as paint pigments. Exposure to toluene can cause eye and nose irritation, tiredness, confusion, euphoria, dizziness, headache, dilated pupils, tears, anxiety, muscle fatigue, insomnia, nerve damage, inflammation of the skin, and liver and kidney damage It is a good solvent (a substance that can dissolve other substances). Toluene toxicity refers to the harmful effects caused by toluene on the body. If you work in an industry that uses toluene, please read chemical labels and the accompanying Safety Data Sheets for hazard information. These chemicals are used in spray-applied sealants and coatings. Toluene exposure can be unintentional or intentional. Toluene occurs naturally in crude oil and in the tolú tree. Identification . Toluene-D8 | C7H8 | CID 74861 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more. Toluene Safety Data Sheet according to Federal Register / Vol. Workers may be harmed from exposure to toluene. When toluene is spilled on the ground or improperly disposed of, it can seep into soil and contaminate nearby wells and streams. Toluene. It is considered an aromatic solvent because it possesses a benzene ring in which six carbon atoms connect with each other from alternating double bonds that create a hexagonal ring called a benzene ring. Toluene is a toxic chemical used in in nail products and hair dyes. It is also widely used for various industrial purposes. It is a mono-substituted benzene derivative, consisting of a methyl group (CH₃) attached to a phenyl group. Sigma-Aldrich offers a number of Toluene products. Toluene is the main chemical that causes many of the signs and symptoms seen with inhalation of glue and paint. von Sirel. Provides assistance and information about the management of occupational exposures to toluene. Toluene is a common ingredient in degreasers. It’s used in paints, dyes, solvents, fingernail polish, and gasoline. A volatile petrochemical solvent and paint thinner, toluene is a potent neurotoxicant that acts as an irritant, impairs breathing, and causes nausea. What are the most important things to know about toluene in an emergency? Toluene has been used as an ingredient in nail polish removers, due to its ability to help dissolve other substances, such as resins and plasticizers. Its main uses are as a raw material for industry, and as a solvent – it can dissolve paint, rubber, ink, and adhesives. A bulk solvent exporter would normally distribute this solvent in bulk vessels or tank trucks. Toluene is a flammable, colorless liquid with an aromatic hydrocarbon odor. Toluene definition is - a liquid aromatic hydrocarbon C7H8 that resembles benzene but is less volatile, flammable, and toxic and is used especially as a solvent, in … Another correct answer is that toluene is an aromatic compound. Its chemical formula is C 7 H 8.Toluene is a commonly used solvent and diluent in paint, paint thinner, and certain glues, where it is responsible for those substances' characteristic odors. Toluene. See more. Toluene Safety Data Sheet according to Federal Register / Vol. Work. Toluene vapor has a sharp or sweet odor, which is a sign of exposure. That's how it smells, too. Toluene 108-88-3 Hazard Summary Toluene is added to gasoline, used to produce benzene, and used as a solvent. The oral LD(50) for toluene in rats is 7.53 ml/kg (Smyth, Carpenter, Weil et al. Its chemical formula is C 7 H 8.Toluene is a commonly used solvent and diluent in paint, paint thinner, and certain glues, where it is responsible for those substances' characteristic odors. You will be subject to the destination website's privacy policy when you follow the link. Exposure to toluene may occur from breathing ambient or indoor air affected by such sources. Mother’s exposure to toluene vapors during pregnancy may cause developmental damage in the fetus. This page links to additional information about: Provides information on training workers who use materials containing toluene about the health and safety hazards of toluene, how to recognize exposure to toluene, and the protective measures that apply to the use of toluene in the specific work area. The central nervous system (CNS) is the primary target organ for toluene toxicity in both humans and animals for acute (short-term) and chronic (long-term) exposures. It is also added to gasoline to improve its octane rating. Products that contain toluene can release the chemical into the air, where it can be inhaled. It is produced in the process of making gasoline and other fuels from crude oil and in making coke from coal. Occupational Safety & Health Administration, Occupational Safety and Health Administration, Authoritative Risk Assessment Information from U.S. Government Agencies, Severe Storm and Flood Recovery Assistance. Toluene: Toluene has a sweet, pungent odor. Toluene is a toxic chemical used in in nail products and hair dyes. Toluene formula is C 6 H 5 CH 3. Both toluene and xylene are important organic compounds having closely similar chemical structures. This means it's made up of carbon and hydrogen atoms, with a formula of C7H8. What is toluene. How does exposure to toluene occur? FOUND IN: Nail polish, nail treatment, hair dyes 77, No. Toluene is also flammable, and its vapors can be ignited by flames, sparks or other ignition sources. Useful search terms for toluene include “methyl benzene,” “methyl benzol,” “phenyl methane,” and “toluol.”. Its other name is methylbenzene, and chemists illustrate it by drawing a six-sided benzene ring and adding a methyl group to it. The odor of toluene is sweet, pungent, benzene-like and gives a smell of paint thinner. What is the WHMIS 1988 classification? It is colorless and insoluble in water. Toluene, which is also known as toluol, is a colourless solution which smells a little like paint thinner. Description of substance: Colorless liquid with a sweet, pungent, benzene-like odor. 58 / Monday, March 26, 2012 / Rules and Regulations Date of issue: 03/21/2014 Revision date: … Toluene has intoxicating properties and when inhaled, can cause neurological harm. Visit NIOSH’s page on Managing Chemical Safety in the Workplace to learn more about controlling chemical workplace exposures. Toluene also is an ingredient in some consumer products such as paints, glues and nail polish removers. In high doses, it … Symptoms worsen as exposure increases, and long term exposure may lead to tiredness, slow reaction, difficulty sleeping, numbness in the hands or feet, or female reproductive system damage and pregnancy loss. Linking to a non-federal website does not constitute an endorsement by CDC or any of its employees of the sponsors or the information and products presented on the website. It has the smell that is often associated with paint thinners. In short, it's a type of paint thinner, or, if you want to get technical, an industrial solvent. What are other names or identifying information for toluene? It can also be used to manufacture other chemicals such as phenol, nitrobenzene, benzoic acid and benzyl chloride. Current OSHA PEL: 200 ppm TWA, 300 ppm CEILING, 1989 OSHA PEL: 100 ppm (375 mg/m 3) TWA, 150 ppm (560 mg/m 3) STEL. Toluene occurs naturally in crude oil and in the tolu tree. Toluene is a solvent used to make some paint thinners, adhesives, and nail care products. Molar Mass. Aromatic means that it's a member of the benzene family. MP3-Download Mit Music Unlimited anhören. CDC twenty four seven. See more. What are the most important things to know about toluene in an emergency? Toluene: The molar mass of toluene is about 92.14 g/mol. Toluene is an aromatic hydrocarbon solvent and natural sources of toluene include crude oil and small quantities it is found in tolu tree.Toluene alternative names include methylbenzene, toluol, anisen, phenyl methane. The Health Hazard Evaluation Program (HHE) conducts onsite investigations of possible worker exposure to chemicals. Wikipedia Toluene is a colourless liquid and water-insoluble liquid. It comprises 15–20 percent of coal-tar light oil and is a minor constituent of petroleum. Toluene is an organic chemical compound having the chemical formula C 7 H 8 and is considered a hydrocarbon because it contains only carbon and hydrogen atoms. It has also been used in the formulation of nail products to enable nail polishes, hardeners and lacquers to be applied smoothly. Toluene is a clear, colorless liquid with a distinctive smell. Toluene (C₆H₅CH₃) is a colorless liquid with a sweet, pungent odor. Products that contain toluene can release the chemical into the air, where it can be inhaled. Toluene is volatile meaning that it disperses into the air and can thereby be inhaled. Before this question can be answered you must explain why you need the answer. TOLUENE DIISOCYANATE is explosive in the form of vapor-air mixture when exposed to heat, flame or sparks. Toluene is produced during the process of making gasoline and other fuels from crude oil, in making coke from coal, and as a by-product in the manufacture of styrene. Toluene vapor has a sharp or sweet odor, which is a sign of exposure. Insoluble in water, it is a colorless liquid with an odor similar to that of paint thinners. Without proper ventilation and safety precautions, toluene can cause irritated eyes, nose, and throat; dry or cracked skin; headache, dizziness, feeling of being drunk, confusion and anxiety. Colorless and insoluble in water, toluene can be dangerous when its fumes are inhaled, causing neurological damage and intoxication. The NIOSH Manual of Analytical Methods (NMAM) is a collection of methods for sampling and analysis of contaminants in workplace air, and in the blood and urine of workers who are occupationally exposed. Exposure to toluene can cause eye and nose irritation, tiredness, confusion, euphoria, dizziness, headache, dilated pupils, tears, anxiety, muscle fatigue, insomnia, nerve damage, … 77, No. The TLV … Toluol, Trivialname nach IUPAC auch Toluen, Methylbenzol, Phenylmethan, nach IUPAC-Nomenklatur Methylbenzen genannt, ist eine farblose, charakteristisch riechende, flüchtige Flüssigkeit, die in vielen ihrer Eigenschaften dem Benzol ähnelt. Toluene (C₆H₅CH₃) is a colorless liquid with a sweet, pungent odor. Odor. 1.1. Biological use: Toluene can also be used for biological purposes. Toluene definition is - a liquid aromatic hydrocarbon C7H8 that resembles benzene but is less volatile, flammable, and toxic and is used especially as a solvent, in … Toluene (), also known as toluol (), is an aromatic hydrocarbon. It's a colorless liquid with a sweet smell and taste. Toluene is produced during the process of making gasoline and other fuels from crude oil, in making coke from coal, and as a by-product in the manufacture of styrene. Both these are aromatic compounds containing benzene rings and attached methyl group(s). As a solvent, toluene can be used in paints, paint thinners, adhesives, inks, resins, cleaning agents, leather tanners and inks. Some examples of workers at risk of being exposed to toluene include the following: NIOSH recommends that employers use Hierarchy of Controls to prevent injuries. Toluene is an aromatic hydrocarbon. It is categorized as such because of the presence of carbon (C) atoms in its chemical formula, C7H8. Exposure to toluene may occur from breathing ambient or indoor air affected by such sources. Toluol ist ein aromatischer Kohlenwasserstoff, häufig ersetzt es als Lösungsmittel das giftige Benzol. Toluene, also known as methylbenzene, is an organic chemical compound. The acute toxicity of toluene in animals is greater than that of benzene. The TLV for toluene was established to protect against subclinical changes in color vision and the potential for spontaneous abortion in female workers. COVID-19 is an emerging, rapidly evolving situation. ; 2,6-Diaminotoluene, a common impurity in 2,4-diaminotoluene; 2,5-Diaminotoluene, precursor to hair dyes. An answer is that toluene is benzene with a methyl group stuck on it. Solvents such as toluene should be stored in drummed containers such as isotanks made of stainless steel, aluminium or carbon steel. Toluene should be kept out of direct sunlight, heat and open flames. View information & documentation regarding Toluene, including CAS, MSDS & more. Toluenediamine may refer to these isomeric organic compounds with the formula C 6 H 3 (NH 2) 2 (CH 3): . Toluene is an aromatic hydrocarbon consisting of a CH 3 group attached to a phenyl ring. Toluene exposures have been studied in nail salons and printing establishments, auto repair, and construction activities. Doğum Günün Kutlu Olsun Tolun. The main chemical use of toluene is to make benzene, xylenes and other solvents. Toluene is typically used in a mixture with other solvents and chemicals such as paint pigments. What products containing TDI and related compounds are available to consumers? Exposure to toluene can result in temporary effects such as headaches, dizziness and cracked skin, as well as more serious effects such as reproductive damage and respiratory complications. Many of the products we rely upon every day are safer and more comfortable through the use of polyurethanes made possible by diisocyanates. The Centers for Disease Control and Prevention (CDC) cannot attest to the accuracy of a non-federal website. Toluene, also known as methylbenzene, is a clear, colorless liquid with a distinctive sweet smell that is widely used in industrial settings as a solvent. The key difference between toluene and xylene is that toluene contains one methyl group attached to a benzene ring whereas xylene contains two methyl groups attached to a benzene ring.. Toluene, aromatic hydrocarbon used extensively as starting material for the manufacture of industrial chemicals. It is a mono-substituted benzene derivate. Consumers could be exposed to these chemicals while using products containing uncured or unhardened TDI and its related compounds. Toluene is added to gasoline, used to produce benzene, and used as a solvent. Toluene, or also known as toluol, is an aromatic hydrocarbon. Highlights specific OSHA standards which may cover the use of toluene in the workplace. Workers can be exposed to toluene by breathing it in, getting it on their skin, getting it splashed into their eyes, or swallowing it. Products that may contain toluene-such as paint, metal cleaners and adhesives-are used in many industries and can be found in many workplaces. Potentially violent polymerization reaction with strong bases or acyl chlorides. An answer is that toluene is benzene with a methyl group stuck on it. Toluene is a clear, colorless liquid with a distinctive smell. Toluene definition, a colorless, water-insoluble, flammable liquid, C7H8, having a benzenelike odor, obtained chiefly from coal tar and petroleum: used as a solvent in the manufacture of benzoic acid, benzaldehyde, TNT, and other organic compounds. Toluene definition, a colorless, water-insoluble, flammable liquid, C7H8, having a benzenelike odor, obtained chiefly from coal tar and petroleum: used as a solvent in the manufacture of benzoic acid, benzaldehyde, TNT, and other organic compounds. Its IUPAC systematic name is methylbenzene. That use of Toluene was first pioneered by the Honda team. It has the strong and sweet smell of paint thinner, but this isn't what makes it aromatic. The central nervous system (CNS) is the primary target organ for toluene toxicity in both humans and animals for acute (short-term) and chronic (long-term) exposures. OSHA's exposure limits for toluene have been set to prevent effects of long term exposure on the nervous system, however, workers frequently experience symptoms of toluene exposure in activities where exposures are lower than OSHA's present exposure limits. Toluene. Patty (1963b, as cited in ACGIH 1986/Ex. It is smell like paint thinners. CDC is not responsible for Section 508 compliance (accessibility) on other federal or private website. Toluene is a clear, colorless liquid which becomes a vapor when exposed to air at room temperature. Gasoline and other fuels also contain toluene. But how is toluene made? Effective way to dry toluene you have to distill it first.. Then take it in umber colored bottle & dry adding sodium wire using sodium press , cork tightly & keep it for 2 to 3 days. Toluene is an aromatic solvent that is primarily used as a thinner or diluent in several end-user products, such as paints, coatings and cleaners. Before this question can be answered you must explain why you need the answer. Search the HHE database for more information on chemical topics. The application of TLV's is discussed in the Statement of Position Regarding the TLVs and BEIs. Diisocyanates are a family of chemical building blocks mainly used to make polyurethane products, such as rigid and flexible foams, coatings, adhesives, sealants and elastomers. Toluene is an aromatic hydrocarbon solvent and natural sources of toluene include crude oil and small quantities it is found in tolu tree.Toluene alternative names include methylbenzene, toluol, anisen, phenyl methane. What are other names or identifying information for toluene? Reaction with aniline may generate enough heat to ignite unreacted portion and surrounding materials. Products with this Ingredient What is Toluene used for? Toluene. Toluene was first derived from reagent named Tolu Balsam. The NIOSH Pocket Guide to Chemical Hazards (NPG) helps workers, employers, and occupational health professionals recognize and control workplace chemical hazards. Chemicals such as paint, metal cleaners and adhesives-are used in a mixture with other and. Nail salons and printing establishments, auto repair, and nail polish removers on! Toluene on the body substance name: toluene is an aromatic compound of steel. And more comfortable through the use of toluene is about 78.11 g/mol can be inhaled and printing establishments auto... And kidney damage flames, sparks or other ignition sources ACGIH 1986/Ex acute... To enable nail polishes, hardeners and lacquers to be applied smoothly 's made up of carbon ( C atoms. 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