对苯二甲酸二丙烯酯 | 1026-92-2

• 物质功能分类: 生物 - 细胞培养 - 添加剂
• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: 对苯二甲酸二丙烯酯
• 中文别名: 对苯二甲酸二烯丙酯
• 英文名称: diallyl terephthalate
• 英文别名: Diallylterephthalat；bis(prop-2-enyl) benzene-1,4-dicarboxylate
• CAS: 1026-92-2
• 化学式: C₁₄H₁₄O₄
• mdl: MFCD00080462
• 分子量: 246.263
• InChiKey: ZDNFTNPFYCKVTB-UHFFFAOYSA-N

物化性质

• 沸点：
  176-178°C 8mm
• 密度：
  1,121 g/cm3
• 闪点：
  171°C

计算性质

• 辛醇/水分配系数(LogP)：
  2.9
• 重原子数：
  18
• 可旋转键数：
  8
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.142
• 拓扑面积：
  52.6
• 氢给体数：
  0
• 氢受体数：
  4

安全信息

• 危险等级：
  6.1
• 危险品运输编号：
  UN 2810
• 海关编码：
  2917399090
• 包装等级：
  III
• 危险类别：
  6.1
• 储存条件：
  2-8°C

SDS

Diallyl Terephthalate Revision number: 5
SAFETY DATA SHEET

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Section 1. IDENTIFICATION
Product name: Diallyl Terephthalate

Revision number: 5

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Section 2. HAZARDS IDENTIFICATION
GHS classification
PHYSICAL HAZARDS Not classified
HEALTH HAZARDS
Acute toxicity (Oral) Category 4
Category 2
Skin corrosion/irritation
Serious eye damage/eye irritation Category 2A
Not classified
ENVIRONMENTAL HAZARDS
GHS label elements, including precautionary statements
Pictograms or hazard symbols
Signal word Warning
Hazard statements Harmful if swallowed
Causes skin irritation
Causes serious eye irritation
Precautionary statements:
Do not eat, drink or smoke when using this product.
[Prevention]
Wash hands thoroughly after handling.
Wear protective gloves/eye protection/face protection.
[Response] IF SWALLOWED: Call a POISON CENTER or doctor/physician if you feel unwell.
Rinse mouth.
IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses,
if present and easy to do. Continue rinsing.
If eye irritation persists: Get medical advice/attention.
IF ON SKIN: Gently wash with plenty of soap and water.
If skin irritation occurs: Get medical advice/attention.
Take off contaminated clothing and wash before reuse.
[Disposal] Dispose of contents/container through a waste management company authorized by
the local government.

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Section 3. COMPOSITION/INFORMATION ON INGREDIENTS
Substance/mixture: Substance
Components: Diallyl Terephthalate
>98.0%(GC)
Percent:
CAS Number: 1026-92-2
Diallyl Terephthalate

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Section 3. COMPOSITION/INFORMATION ON INGREDIENTS
Synonyms: Terephthalic Acid Diallyl Ester
Chemical Formula: C14H14O4

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Section 4. FIRST AID MEASURES
Remove victim to fresh air and keep at rest in a position comfortable for breathing.
Inhalation:
Get medical advice/attention if you feel unwell.
Remove/Take off immediately all contaminated clothing. Gently wash with plenty of
Skin contact:
soap and water. If skin irritation or rash occurs: Get medical advice/attention.
Rinse cautiously with water for several minutes. Remove contact lenses, if present
Eye contact:
and easy to do. Continue rinsing. If eye irritation persists: Get medical
advice/attention.
Ingestion: Call a POISON CENTER or doctor/physician if you feel unwell. Rinse mouth.
Protection of first-aiders: A rescuer should wear personal protective equipment, such as rubber gloves and air-
tight goggles.

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Section 5. FIRE-FIGHTING MEASURES
Suitable extinguishing Dry chemical, foam, water spray, carbon dioxide.
media:
Unsuitable extinguishing Solid streams of water
media:
Precautions for firefighters: Fire-extinguishing work is done from the windward and the suitable fire-extinguishing
method according to the surrounding situation is used. Uninvolved persons should
evacuate to a safe place. In case of fire in the surroundings: Remove movable
containers if safe to do so.
Special protective When extinguishing fire, be sure to wear personal protective equipment.
equipment for firefighters:

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Section 6. ACCIDENTAL RELEASE MEASURES
Use personal protective equipment. Keep people away from and upwind of spill/leak.
Personal precautions,
protective equipment and Ensure adequate ventilation. Entry to non-involved personnel should be controlled
emergency procedures: around the leakage area by roping off, etc.
Environmental precautions: Prevent product from entering drains.
Methods and materials for Absorb spilled material in a suitable absorbent (e.g. rag, dry sand, earth, saw-dust).
containment and cleaning In case of large amount of spillage, contain a spill by bunding. Adhered or collected
up: material should be promptly disposed of, in accordance with appropriate laws and
regulations.

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Section 7. HANDLING AND STORAGE
Precautions for safe handling
Technical measures: Handling is performed in a well ventilated place. Wear suitable protective equipment.
Prevent generation of vapour or mist. Wash hands and face thoroughly after
handling.
Use a ventilation, local exhaust if vapour or aerosol will be generated.
Advice on safe handling: Avoid contact with skin, eyes and clothing.
Conditions for safe storage, including any
incompatibilities
Storage conditions: Keep container tightly closed. Store in a refrigerator.
Store away from incompatible materials such as oxidizing agents.
Heat-sensitive, Light-sensitive
Packaging material: Comply with laws.

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Section 8. EXPOSURE CONTROLS / PERSONAL PROTECTION
Engineering controls: Install a closed system or local exhaust as possible so that workers should not be
exposed directly. Also install safety shower and eye bath.
Personal protective equipment
Respiratory protection: Vapor respirator. Follow local and national regulations.
Diallyl Terephthalate

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Section 8. EXPOSURE CONTROLS / PERSONAL PROTECTION
Hand protection: Protective gloves.
Eye protection: Safety glasses. A face-shield, if the situation requires.
Skin and body protection: Protective clothing. Protective boots, if the situation requires.

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Section 9. PHYSICAL AND CHEMICAL PROPERTIES
Physical state (20°C): Liquid
Clear
Form:
Colour: Colorless - Very pale yellow
Odour: No data available
pH: No data available
Melting point/freezing point:No data available
Boiling point/range: 172°C/0.7kPa
Flash point: 158°C
Flammability or explosive
limits:
Lower: No data available
Upper: No data available
Relative density: 1.12
Solubility(ies):
[Water] No data available
[Other solvents] No data available

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Section 10. STABILITY AND REACTIVITY
Stable under proper conditions.
Chemical stability:
Possibility of hazardous No special reactivity has been reported.
reactions:
Incompatible materials: Oxidizing agents
Hazardous decomposition Carbon monoxide, Carbon dioxide
products:

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Section 11. TOXICOLOGICAL INFORMATION
Acute Toxicity: No data available
Skin corrosion/irritation: No data available
Serious eye No data available
damage/irritation:
Germ cell mutagenicity: No data available
Carcinogenicity:
IARC = No data available
NTP = No data available
Reproductive toxicity: No data available

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Section 12. ECOLOGICAL INFORMATION
Ecotoxicity:
Fish: No data available
No data available
Crustacea:
Algae: No data available
Persistence / degradability: No data available
Bioaccumulative No data available
potential(BCF):
Mobility in soil
Log Pow: No data available
Soil adsorption (Koc): No data available
No data available
Henry's Law
constant(PaM3/mol):
Diallyl Terephthalate

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Section 13. DISPOSAL CONSIDERATIONS
Recycle to process, if possible. Consult your local regional authorities. You may be able to burn in a chemical
incinerator equipped with an afterburner and scrubber system. Observe all federal, state and local regulations when
disposing of the substance.

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Section 14. TRANSPORT INFORMATION
Hazards Class: Does not correspond to the classification standard of the United Nations
UN-No: Not listed

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Section 15. REGULATORY INFORMATION
Safe management ordinance of dangerous chemical product (State Council announces on January 26, 2002
and revised on February 16,2011): Safe use and production, the storage of a dangerous chemical, transport,
loading and unloading were prescribed.

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SECTION 16 - ADDITIONAL INFORMATION
N/A

反应信息

• 作为反应物：
  描述：

  对苯二甲酸二丙烯酯 在 dihydrogen hexachloroplatinate 、 尿素 作用下， 以 异丙醇 、 苯 为溶剂， 生成 Terephthalic acid 1-allyl ester 4-[3-(methoxy-dimethyl-silanyl)-propyl] ester
  参考文献：
  名称：

  Andrianov,K.A. et al., Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, 1968, p. 797 - 798

  摘要：

  DOI：
• 作为产物：
  描述：

  对苯二甲酸二甲酯 生成 对苯二甲酸二丙烯酯
  参考文献：
  名称：

  Di(aromatic) compounds and their use in human and veterinary medicine

  摘要：

  对应以下公式的二芳基化合物：##STR1## 其中：Ar代表##STR2## n=1或2或：##STR3## X代表二价基团，Z代表O、S或二价基团，R.sub.1、R.sub.2、R.sub.3、R.sub.4和R.sub.5代表氢原子或各种有机基团，以及当R.sub.1是羧酸功能时，公式（I）化合物的盐。用于人类和兽医学以及化妆品。

  公开号：

  US05387594A1

文献信息

• SUBSTITUTED OR UNSUBSTITUTED ALLYL GROUP-CONTAINING MALEIMIDE COMPOUND, PRODUCTION METHOD THEREFOR, AND COMPOSITION AND CURED PRODUCT USING SAID COMPOUND
  申请人：DIC CORPORATION

  公开号：US20200325101A1

  公开（公告）日：2020-10-15

  Bismaleimides (BMI) exhibit excellent heat resistance (high Tg and high resistance to thermal decomposition) compared to epoxy resins and phenolic resins, and therefore, in recent years, more attention is paid to bismaleimides as a resin material for the next-generation devices represented by SiC power semiconductors, in addition to the investigation on the use of bismaleimides for electronic material applications. As such, conventional BMI's are known as highly heat-resistant resins; however, there is a demand for a resin having higher heat resistance for advanced material applications and the like. Thus, an object of the invention is to provide a novel maleimide compound having superior heat resistance. Disclosed is a substituted or unsubstituted allyl group-containing maleimide compound having a structure with three or more benzene rings, having one or more groups each having a substituted or unsubstituted allyl group, and having one or more maleimide groups.

  亚苯基马来酰亚胺化合物，具有三个或更多苯环的结构，含有一个或多个取代或未取代的烯丙基团，以及一个或多个马来酰亚胺基团，具有卓越的耐热性。
• Efficient Synthesis of Macrocyclic Paracyclophanes by Ring-Closing Metathesis Dimerization and Trimerization Reactions
  作者：Jinsung Tae、Young-Keun Yang

  DOI：10.1021/ol027557z

  日期：2003.3.1

  para-disubstituted aromatic substrates produced macrocyclic [n.n]-, and [n.n.n]paracyclophanes efficiently through dimerization and trimerization reactions. Sufficiently long alkyl chains allowed direct monocyclizations to yield [n]paracyclophanes. A small library of paracyclophanes were generated by the combinatorial cross-metathesis approach.

  对二取代芳族底物的闭环易位反应通过二聚和三聚反应有效地产生了大环[nn]-和[nnn]对环环烷。足够长的烷基链允许直接单环化产生[n]对环环烷。通过组合交叉复分解方法生成了一个小的对环烷烃库。
• SYSTEM FOR PROTECTING GOODS DURING TRANSPORT
  申请人：Stutz Susanne

  公开号：US20120328685A1

  公开（公告）日：2012-12-27

  A system for protecting stored goods in a container ( 10 ), comprises a cage-like structure ( 20 ) formed by at least one pesticide treated net ( 22 ), capable of enclosing the stored goods, wherein the cage like structure ( 20 ), further comprises means for suspending the pesticide treated nets ( 14, 28, 30, 32, 34 ), and means for opening and closing the cage-like structure ( 26 ) on at least one section ( 24 ) of the at least one net ( 22 ). The system is particularly useful for the transport of tobacco, coffee, dried fruits, cocoa, nuts, tea, cereals, vegetables, spices and animals.

  一个用于保护集装箱（10）中存放货物的系统，包括由至少一种经过杀虫剂处理的网（22）形成的类似笼子的结构（20），能够围住存放的货物，其中类似笼子的结构（20）进一步包括用于悬挂经过杀虫剂处理的网（14、28、30、32、34）的手段，以及用于在至少一种网（22）的至少一部分（24）上打开和关闭类似笼子结构（26）的手段。该系统特别适用于烟草、咖啡、干果、可可、坚果、茶叶、谷物、蔬菜、香料和动物的运输。
• Photochromic Compound
  申请人：Yokoyama Yasushi

  公开号：US20090299080A1

  公开（公告）日：2009-12-03

  [Problem] To provide a photochromic compound that is rapidly colored upon irradiation with ultraviolet light, and is rapidly decolored rapidly upon heat application after termination of irradiation with ultraviolet light, and to provide a process for producing the same. [Means for Solving Problems] A photochromic compound represented by general formula (I). R 1 , R 2 and R 3 are each a hydrogen atom; a functional group containing an atom in groups 15-16 of the periodic table; a halogen atom; a hydrocarbon group optionally substituted with said functional group or a halogen atom; or an optionally substituted heterocyclic group. R 1 and R 2 as well as R 2 and R 3 may be bonded to each other to form an optionally substituted carbon or heterocyclic ring. Z is a polymantylidene group. W is a divalent organic group that forms an optionally substituted carbon aromatic or heterocyclic aromatic ring together with the carbon-carbon double bond to which it is bonded.

  提供一种光致变色化合物，该化合物在紫外光照射后迅速变色，并在紫外光照射终止后施加热量后迅速褪色的方法，以及提供其制备方法。解决问题的方法是提供一种由通式（I）表示的光致变色化合物。R1、R2和R3分别为氢原子；包含周期表第15-16族中的原子的官能团；卤素原子；可选择地用所述官能团或卤素原子取代的碳氢基团；或可选择地取代的杂环基团。R1和R2以及R2和R3可以相互连接以形成可选择地取代的碳环或杂环。Z为多曼特基团。W为二价有机基团，与其相结合的碳-碳双键形成可选择地取代的碳芳香或杂环芳香环。
• DENTAL ADHESIVE COMPOSITION
  申请人：Matsushige Koji

  公开号：US20120238658A1

  公开（公告）日：2012-09-20

  [Problems] To provide a liquid dental adhesive composition which contains a phosphoric acid-type compound having a hydrogenphosphoric diester group as an acidic group-containing polymerizable monomer and, further, contains polyvalent metal ions, effectively preventing not only the gelation but also the formation of precipitates (cloudiness) during the storage. [Means for Solution] A dental adhesive composition which is acidic and contains an acidic group-containing polymerizable monomer (A), polyvalent metal ions (B), water (C), a water-soluble organic solvent (D) and fluoride ions (E), wherein at least 35% by mole of the acidic group-containing polymerizable monomer (A) is a phosphoric acid-type compound having a hydrogenphosphoric diester group, and the contents of the fluoride ions (E) and the polyvalent metal ions (B) are so set that a valence number ratio (R F ) defined by the following formula (1): R F =V F /TV P (1) wherein V F is a valence number of the fluoride ions (E) contained in the composition, and TV P is a total valence number of the polyvalent metal ions (B) contained in the composition, satisfies a range of 0.2 to 2.0.

  提供一种液体牙科粘合剂组合物，其中包含具有氢磷酸二酯基团作为酸性基团的聚合可单体的磷酸型化合物，并且进一步含有多价金属离子，有效地防止在储存期间不仅凝胶化，还防止沉淀（混浊）的形成。解决方案是一种含有酸性和含有酸性基团的聚合可单体（A）、多价金属离子（B）、水（C）、水溶性有机溶剂（D）和氟离子（E）的牙科粘合剂组合物，其中至少35%的含有酸性基团的聚合可单体（A）是具有氢磷酸二酯基团的磷酸型化合物，并且氟离子（E）和多价金属离子（B）的含量设置得使得以下公式（1）定义的价数比率（RF）满足0.2至2.0的范围：RF=VF/TVP（1）其中VF是组合物中含有的氟离子（E）的价数，而TVP是组合物中含有的多价金属离子（B）的总价数。

表征谱图