Dioctyl phthalate - Substance Information - ECHA
Dioctyl phthalate. Regulatory process names 2 CAS names 1 IUPAC names 3 Other names 1 Other identifiers 2 The substance identifiers displayed in the InfoCard are the best available substance name, EC number, CAS number and/or the molecular and structural formulas. IUPAC names . 1,2-dioctyl benzene-1,2-dicarboxylate . Other . Di-n-octyl
Dioctyl adipate has been detected in wastewater effluents from the pulp and paper industry and in sewage treatment effluents(2,3). Di-n-octyl adipate was detected in effluent irrigation samples collected from Glil-Yam, 15 km north of Tel-Aviv, Israel at a concentration of 1,500 ppb from a depth of 9-10 m(4).
DI-N-OCTYL PHTHALATE | CAMEO Chemicals | NOAA
DI-N-OCTYL PHTHALATE reacts with acids to liberate heat along with alcohols and acids. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Heat is also generated by the interaction with caustic solutions. Flammable hydrogen may be generated by mixing with alkali metals and hydrides.
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Dioctyl isophthalate [ACD/IUPAC Name] Dioctyl-isophthalat [German] [ACD/IUPAC Name] Isophtalate de dioc tyle [French] [ACD/IUPAC Name]
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IUPAC Systematic Name: Bis(2-ethylhexyl) phthalate. Synonyms. : 1,2-Benzenedicarboxylic acid, bis(2-ethylhexyl) ester; 1,2-benzenedicar boxylic acid, 1,2-bis(2-ethylhexyl) ester; bis(2-ethylhexyl) benzene-1,2-dicarboxy late; bis(2-ethylhexyl) 1,2-benzenedicar boxylate; bis(2-ethylhexyl) o.
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1.2.1. Production. DEHP is produced commercially by the reaction of excess 2-ethylhexanol with phthalic anhydride in the presence of an acid catalyst such as sulfuric acid or para-toluenesulfonic acid (ATSDR, 2002).It was first produced in commercial quantities in Japan around 1933 and in the United States of America in 1939 ().World consumption of phthalates in the early 1990s was estimated
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IUPAC name/number. An IUPAC name is based on the international standard chemical nomenclature set by the International Union of Pure and Applied Chemistry (IUPAC). The IUPAC nomenclature is a systematic way of naming chemical substances, both organic and inorganic.
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Di(2-ethylhexyl) phthalate is available in a variety of technical grades (including a special grade for capacitor applications and a low residuals grade). Typical specifications are: minimal ester content, 99.0–99.6%; maximal moisture content, 0.1%; and acidity (as acetic acid or phthalic acid), 0.007–0.01% (Aristech Chemical Corp., 1992; WHO, 1992).
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1.2. Production. Di(2-ethylhexyl) adipate can be prepared by the reaction of adipic acid and 2-ethylhexanol in the presence of an esterification catalyst such as sulfuric acid or para-toluenesulfonic acid (National Library of Medicine, 1999).. Information available in 1999 indicated that di(2-ethylhexyl) adipate was manufactured by eleven companies in Japan, eight companies in the United
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of di(2-ethylhexyl) adipate (less than 0.08 mg/m3) near a cool rod machine (operating temperature of 190°C) used to cut PVC film in a meat cutting and wrapping department of a grocery store (Daniels et al., 1985). 1.4.3 Environmental occurrence Di(2-ethylhexyl) adipate may be released into the environment during its manu-
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Phthalates (or phthalic acid (PA) diesters) high volume chemicals being produced, mainly for the manufacture of polyvinyl chloride (PVC) plastics , and over a dozen phthalates are available on the market to be blended in various consumer goods at different proportions (Table 1, Table 2).Diethylhexyl phthalate (DEHP) is the first phthalate introduced on this globe, which was in late 1920s
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Bis(2-propylheptyl) or Di (2-propylheptyl) phthalate is a phthalate and is the diester of phthalic acid and the 10-carbon branched-chain alcohol 2-propylheptanol. DPHP possesses very good plasticizing properties and may be used as a direct replacement for DEHP and DINP in many applications.
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some chemicals present in industrial and consumer products, food and drinking-water volume 101 this publication represents the views and expert opinions of an iarc working group on the evaluation of carcinogenic risks to humans, phthalate . IUPAC Systematic Name: Bis(2-ethylhexyl)
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In an Italian factory producing n-butyl phthalate, isobutyl phthalate, and DEHP, Gilioli et al. (1978) measured total phthalate exposure concentrations of between 1 and 60 mg/m 3, the average being 5 mg/m 3. Nielsen et al. (1985) measured total phthalic acid esters in air in a PVC-processing plant in Sweden where diisodecyl phthalate, DEHP, and
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IUPAC name/number. An IUPAC name is based on the international standard chemical nomenclature set by the International Union of Pure and Applied Chemistry (IUPAC). The IUPAC nomenclature is a systematic way of naming chemical substances, both organic and inorganic.
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A similar plastic is Polyamide 410 (PA 410), derived 70% from castor oil, under the trade name EcoPaXX, commercialized by DSM. PA 410 is a high-performance polyamide that combines the benefits of a high melting point (approx. 250 °C), low moisture absorption and excellent resistance to various chemical substances.
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List trade names in the box below that you wish to link to as the owner of. New trade names need to be notified to us. AEROSOL Surfactant - range of wetting, emulsifying, dispersing and solubilising agents Air1 ALKON - Anti-Tacks, Sodium & Potassium Soaps.
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IUPAC Name: methyl 2-methoxybenzoate | CAS Registry Number: 606-45-1 Synonyms: Methyl o-anisate, Methyl 2-methoxybenzoate, Dimethyl salicylate, o-Anisic acid, methyl ester, Methyl o-methoxybenzoate, Methyol o-methoxybenzoate, o-Methoxy methyl benzoate, Methoxy methylbenzoate, o-, Methylsalicylate methyl ether, FEMA No. 2717, o-Methoxybenzoic acid methyl ester, Methyl salicylate o-methyl ether
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IUPAC Name: bis(2-methylpropyl) benzene-1,2-dicarboxylate | CAS Registry Number: 84-69-5 Synonyms: DIISOBUTYL PHTHALATE, Palatinol IC, Isobutyl phthalate, Hexaplas M/1B, Kodaflex DIBP, Hatcol DIBP, DIBP, Di-iso-butyl phthalate, Di(i-butyl)phthalate, Phthalic acid, diisobutyl ester, CCRIS 6193, HSDB 5247, MLS000516002, MLS002152902, di-l-butyl phthalate (DIBP), 152641_ALDRICH, 80130_FLUKA, AI3
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Plasticizer. Plasticizers (UK: plasticisers) or dispersants are additives that increase the plasticity or decrease the viscosity of a material. [1] Benzoic acid, Benzyl butyl phthalate, Benzyl chloride, Bindeez, BioAmber, Bioplastic, Bis(2-ethylhexyl) adipate, Bis(2-ethylhexyl) phthalate, Bisphenol A,
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In an Italian factory producing n-butyl phthalate, isobutyl phthalate, and DEHP, Gilioli et al. (1978) measured total phthalate exposure concentrations of between 1 and 60 mg/m 3, the average being 5 mg/m 3. Nielsen et al. (1985) measured total phthalic acid esters in air in a PVC-processing plant in Sweden where diisodecyl phthalate, DEHP, and
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IUPAC name/number. An IUPAC name is based on the international standard chemical nomenclature set by the International Union of Pure and Applied Chemistry (IUPAC). The IUPAC nomenclature is a systematic way of naming chemical substances, both organic and inorganic.
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Bis(2-ethylhexyl) phthalate (di-2-ethylhexyl phthalate, diethylhexyl phthalate, DEHP; dioctyl phthalate, DOP) is an organic compound with the formula C 6 H 4 (CO 2 C 8 H 17) 2. DEHP is the most common member of the class of phthalates, which are used as plasticizers. It is the diester of phthalic acid and the branched-chain 2-ethylhexanol.
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1900164 Copper(II) chloride is the chemical compound with the chemical formula CuCl2. This is a light brown solid, 1900404 Diethyl Phthalate No No 1900405 Â Footwear for women, chemical name 2,5,8,11,14,17-Hexaoxanonadecan-19-ol 19-methanesulfonate (CAS
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Polyhydroxyalkanoate (PHA): Review of synthesis, characteristics, processing and potential applications in packaging Article (PDF Available) in eXPRESS Polymer Letters 8(11):791-808 · June 2014
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Atraric Acid is a naturally occurring phenolic compound and ester with the IUPAC name methyl 2,4-dihydroxy-3,6-dimethylbenzoate and molecular formula C10H12O4. (di-2-ethylhexyl phthalate, diethylhexyl phthalate, DEHP; dioctyl phthalate, DOP) is an organic compound with the formula C6H4(CO2C8H17)2. Antiandrogen and Chemical castration
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Textile Exchange, which administers the new Global Recycle Standard, has introduced what it says is a “minor but important” change in GRS version 2.1, according to the April/May 2012 issue of Ecotextile News. (If you’re wondering what the Global Recycle Standard is all about, please see our blog post on the subject: click here .). The new change removes the allowance for the use of pre
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In the same year, the world harvested ∼115 million metric tons of vegetable oils, of which ∼80, 15, and 5% was consumed for food, chemical products, and animal feed, respectively.28 A sig- nificant portion of the 15% for chemical use included 7.5 million metric tons of high-lauric content coconut and palm kernel oil, approximately half of
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