3 edition of Toluene. found in the catalog.
|Series||Environmental health criteria ;, 52|
|Contributions||United Nations Environmental Program., International Labour Organisation., World Health Organization., International Programme on Chemical Safety.|
|LC Classifications||RA1242.T63 T65 1985|
|The Physical Object|
|Pagination||146 p. :|
|Number of Pages||146|
|LC Control Number||86174550|
DANGER! Emergency Overview Flammable liquid and vapor. Causes eye, skin, and respiratory tract irritation. Vapors may cause drowsiness and dizziness. Aspiration hazard if swallowed - can enter lungs and cause : The ATSDR toxicological profile succinctly characterizes the toxicologic and adverse health effects information for the hazardous substance described here. Each peer-reviewed profile identifies and reviews the key literature that describes a hazardous substance's toxicologic properties. Other pertinent literature is also presented, but is described in less detail than the key studies.
Toluene is used in the manufacture of benzene, p-xylene for polyethylene terephthalate (PET) resins, and toluene diisocyanates (TDI) for polyurethane applications, and is widely used as a solvent. The majority of toluene production is unrecovered (i.e., not isolated from other aromatic constituents) and is consumed as a constituent of various. Exposure to toluene does not result in the hematopoietic effects caused by benzene. Most of the toluene introduced in the body by inhalation is metabolized to benzoic acid, which is. 3 of 40 TFVM. conjugated with glycine in the liver to form hippuric acid. The hippuric acid is then excretedFile Size: 1MB.
Toluene will enter the body if we breathe in contaminated air, breathe in tobacco smoke, or consume food or water that contains toluene. It can also be absorbed through the skin, if liquid toluene is in contact with the skin. Human exposure occurs mainly by breathing air containing toluene. Toluene usually leaves the body with in twelve hours. Discover the best Toluene books and audiobooks. Learn from Toluene experts like Elsevier Books Reference and Frontiers. Read Toluene books like Halogenated Benzenes, Toluenes and Phenols with Water and for free with a free day trial.
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Symbol which looks like a small house Solid circle with an upward pointer in it. Jump to content. Toluene. book c (K) Reference Comment; ± Tsonopoulos and Ambrose, Chirico and Steele, Uncertainty assigned by TRC = 1.
K; TRC Teja and. Toluene | C6H5CH3 or C7H8 | CID - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety.
Toluene. Related Pages. Synonyms & Trade Names Methyl benzene, Methyl benzol, Phenyl methane, Toluol CAS No. RTECS No. XS DOT ID & Guide.
Formula. C₆H₅CH₃. Toluene is added to gasoline, used to produce benzene, and used as a solvent. Exposure to toluene may occur from breathing ambient or indoor air affected by such sources. 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.
Book Page. Optical constants of C 7 Optical constants of C 7 H 8 (Toluene) Kedenburg et al. n µm, k µm. Wavelength: µm ( – ) Complex refractive index (n+ik) Toluene, C 7 H 8 Other names. Methylbenzene; Phenylmethane; Toluol; Anisen; External links. Toluene is an aromatic hydrocarbon (a methyl-substituted benzene derivative), which occurs as a clear colorless volatile liquid and possesses a pungent, benzene-like odor.
Toluene is water insoluble but is miscible with other organic solvents. It is routinely added to gasoline as an additive along with benzene Toluene. book xylene to increase the octane.
Toluene is Toluene. book major component of tobacco smoke and concentrations can vary greatly. The concentration per cigarette in sidestream smoke is typically higher than in mainstream smoke.
The amount of toluene in mainstream smoke from an unfiltered cigarette was estimated to range from to µg with a sidestream/mainstream smoke ratio of (23).
Book Page. Optical constants of C 7 Optical constants of C 7 H 8 (Toluene) Kozma et al. n µm. Wavelength: µm ( – ) Complex refractive index (n+ik) Toluene - Wikipedia; Toluene - NIST Chemistry WebBook; website.
TOLUENE Maximum concentration ppm N/A OSHA Z2 TOLUENE TWA ppm N/A OSHA Z2 TOLUENE TWA 20 ppm N/A ACGIH NOTE: Limits/standards shown for guidance only.
Follow applicable regulations. Page 6 of 16 MSDS - Toluene ENGINEERING CONTROLS The level of protection and types of controls necessary will vary depending File Size: KB. Toluene is also called as toluol, is an aromatic hydrocarbon.
It is first isolated in by distillation of pine oil by a Polish chemist named Filip Walter. It is colorless, water-insoluble and has a smell associated with paint thinners. Toluene can also be used as a recreational inhalant sometimes, and it also has the potential of causing severe neurological harm.
Toluene, a.k.a. methyl benzene, is a clear, flammable, water-insoluble liquid with the odor of paint thinner. It can be found naturally in petroleum crude oil. Exposure to toluene can occur through air, water, soil, and groundwater, but almost all of the toluene released as emissions is dispersed into the air.
Toluene (C₆H₅CH₃) is a colorless liquid with a sweet, pungent odor. 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.
Additional Physical Format: Online version: Bell, G. Toluene. London: H.M.S.O., (OCoLC) Material Type: Government publication, International. Toluene diisocyanate (TDI) is an organic compound with the formula CH 3 C 6 H 3 (NCO) of the six possible isomers are commercially important: 2,4-TDI (CAS: ) and 2,6-TDI (CAS: ).
2,4-TDI is produced in the pure state, but TDI is often marketed as 80/20 and 65/35 mixtures of the 2,4 and 2,6 isomers respectively.
It is produced on a large scale, accounting for % of the Chemical formula: C₉H₆N₂O₂. Toluene, Meets ACS Specifications, Meets Reagent Specifications for testing USP/NF monographs GR ACS, Toluene, for gas chromatography ECD and FID SupraSolv®. Toluene, a flammable liquid with a pungent odor, is widely employed as organic solvent.
It is widely used as a precursor for synthesizing benzene and as a solvent in the paint industry. It has been reported to be a biotoxic solvent (toxic to many microorganisms at %v/v concentrations).
Toluene is formed from petroleum by catalytic dehydrogenation of fractions containing methylcyclohexane. Industrial grade toluene is 98% pure and may contain up to 2% xylenes and benzene (DOE, ). Production and Uses A commercial use pattern survey has been completed for toluene (Corpus Information Services, ).
Also known as: Toluol, Methylbenzene, Phenylmethane Chemical reference number (CAS): Toluene is a common ingredient in degreasers. It's a colorless liquid with a sweet smell and taste. It evaporates quickly. Toluene is found naturally in crude oil, and is used in oil refining and the manufacturing of paints, lacquers, explosives (TNT) and glues.
In homes, toluene may be found in. COVID Resources. Reliable information about the coronavirus (COVID) is available from the World Health Organization (current situation, international travel).Numerous and frequently-updated resource results are available from this ’s WebJunction has pulled together information and resources to assist library staff as they consider how to handle coronavirus.
Toluene: Health Information Summary Toluene is a clear, colorless, flammable liquid that is naturally found in petroleum. It is added to gasoline at 5 to 7 percent by weight to improve the octane rating.
It is used as a solvent in paints, adhesives, ink, and cleaning File Size: 52KB.Toluene Safety Data Sheet according to Federal Register / Vol. 77, No. 58 / Monday, Ma / Rules and Regulations Date of issue: 03/21/ Revision File Size: KB.What handling and storage practices should be used when working with toluene?
Handling: In the event of a spill or leak, exit the area immediately. Eliminate heat and ignition sources such as sparks, open flames, hot surfaces and static discharge.