cis-4-シクロヘキセン-1,2-ジカルボン酸無水物(935-79-5)

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cis-4-シクロヘキセン-1,2-ジカルボン酸無水物 製品概要
化学名:cis-4-シクロヘキセン-1,2-ジカルボン酸無水物
英語化学名:cis-1,2,3,6-Tetrahydrophthalic anhydride
别名:1,3-isobenzofurandion,3a,4,7,7a-tetrahydro-,cis-;3-Isobenzofurandione,3a,4,7,7a-tetrahydro-,cis-1;4,7,7a-tetrahydro-3-isobenzofurandioncis-3a;cis-3a,4,7,7a-Tetrahydro-1,3-isobenzofurandione;CIS-THPA;CIS-DELTA4-TETRAHYDROPHTHALIC ANHYDRIDE;CIS-4-TETRAHYDROPHTHALIC ANHYDRIDE;CIS-1,2,3,6-TETRAHYDROPHTHALIC ANHYDRIDE
CAS番号:935-79-5
分子式:C8H8O3
分子量:152.15
EINECS:213-308-7
カテゴリ情報:Diels-Alder Adducts
Mol File:935-79-5.mol
cis-4-シクロヘキセン-1,2-ジカルボン酸無水物
cis-4-シクロヘキセン-1,2-ジカルボン酸無水物 物理性質
融点 98 °C
沸点 234.6°C (rough estimate)
比重(密度) 1.2143 (rough estimate)
蒸気密度5.2 (vs air)
蒸気圧<0.01 mm Hg ( 20 °C)
屈折率 1.4447 (estimate)
闪点 156 °C
貯蔵温度 under inert gas (nitrogen or Argon) at 2-8°C
溶解性soluble in Toluene,Benzene
外見 powder to crystal
White to Almost white
水溶解度 REACTS
Sensitive Moisture Sensitive
BRN 82341
暴露限界値ACGIH: TWA 0.01 mg/m3
OSHA: TWA 0.25 ppm(1 mg/m3)
NIOSH: IDLH 10 mg/m3; TWA 0.25 ppm(1 mg/m3)
CAS データベース935-79-5(CAS DataBase Reference)
NISTの化学物質情報cis-1,2,3,6-Tetrahydrophthalic anhydride(935-79-5)
EPAの化学物質情報1,3-Isobenzofurandione, 3a,4,7,7a-tetrahydro-, (3aR,7aS)-rel- (935-79-5)
安全性情報
主な危険性 Xn
Rフレーズ 41-42/43-52/53
Sフレーズ 22-24-26-37/39-61-52/53-42/43-41
RIDADR UN 2698 8/PG 3
WGK Germany 3
RTECS 番号GW5775000
TSCA Yes
国連危険物分類 8
容器等級 III
HSコード 29173990
MSDS Information
ProviderLanguage
cis-4-Cyclohexene-1,2-dicarboxylic anhydride English
SigmaAldrich English
ACROS English
ALFA English
cis-4-シクロヘキセン-1,2-ジカルボン酸無水物 Usage And Synthesis
外観白色~わずかにうすい黄色, フレーク
溶解性水に難溶, エタノールに可溶。熱エタノール(99.5)に溶ける。ベンゼンに可溶。エーテル、石油エーテルに微溶。
説明Tetrahydrophthalic anhydride is an organic compound with the formula C6H8C2O3. The compound exists as two isomers, this article being focused on the more common cis isomer. It is a precursor to other compounds including the dicarboxylic acid tetrahydrophthalic acid as well the tetrahydrophthalimide, which is a precursor to the fungicide Captan. It is a white solid that is soluble in organic solvents.
Tetrahydrophthalic anhydride, the cis isomer, is prepared by the Diels-Alder reaction of butadiene and maleic anhydride.
化学的特性Tetrahydrophthalic Anhydride (THPA) is a white crystalline powder or FLAKES. It is slightly soluble in benzene and acetone and it is also sensitive to moisture.
使用cis-1,2,3,6-Tetrahydrophthalic anhydride (THPA) can be used as:
  • A curing agent for epoxides.
  • A chemical modifier in the modification of polystyrene via Friedel-Crafts acylation for enhancing the thermal stability of the polymer.
  • A reactant for the synthesis of cis-tetrahydroisoindole-1,3-dione derivatives and cyclic diimides.

使用Tetrahydrophthalic Anhydride is an anhydride hardener mainly used in the fields of coatings, epoxy resin curing agents, polyester resins, adhesives, plasticizers, pesticides, etc. It is also used as a chemical intermediate for light colored alkyds.
Tetrahydrophthalic Anhydride is an organic compound obtained from the reaction of Maleic Anhydride and Butadiene.
製造方法A flask containing 500 ml of dry benzene and 196 gm (2 moles) of maleic anhydride is heated with a pan of hot water while butadiene is introduced rapidly (0.6-0.8 liter/min) from a commercial cylinder. The solution is stirred rapidly and the heating is stopped after 3-5 min when the temperature reaches 50°C. In 15-25 min the reaction causes the temperature of the solution to reach 70-75°C. The absorption of the rapid stream of butadiene is nearly complete in 30-40 min. The addition of butadiene is continued at a slower rate for a total of 2\ hr. The solution is poured into a 1-liter beaker which is covered and kept at 0-5°C overnight. The product is collected on a large Buchner funnel and washed with 250 ml of b.p. 35-60°C petroleum ether. A second crop is obtained by diluting the filtrate with an additional 250 ml of petroleum ether. Both crops are dried to constant weight in an oven at 70-80°C to yield 281.5-294.5 gm (96- 97%, m.p. 99-102°C). Recrystallization from ligroin or ether raises the melting point to 103-104°C.
Preparation of Tetrahydrophthalic Anhydride
Synthesis Reference(s)Journal of the American Chemical Society, 64, p. 802, 1942 DOI: 10.1021/ja01256a018
Tags:935-79-5