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Merck
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文件

454338

Sigma-Aldrich

二聚环戊二烯

contains BHT as stabilizer

别名:

4,7-亚甲基-3a,4,7,7a-四氢茚, DCPD, 环戊二烯二聚体

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About This Item

经验公式（希尔记法）:
C10H12
CAS号:
77-73-6
分子量:
132.20
Beilstein:
1904092
EC號碼:
201-052-9
MDL號碼:
MFCD00078246
分類程式碼代碼:
12352100
PubChem物質ID:
24868570
NACRES:
NA.22

包含

BHT as stabilizer

品質等級

200

bp

170 °C (lit.)

mp

33 °C (lit.)

密度

0.986 g/mL at 25 °C (lit.)

SMILES 字串

C1C=CC2C3CC(C=C3)C12

InChI

1S/C10H12/c1-2-9-7-4-5-8(6-7)10(9)3-1/h1-2,4-5,7-10H,3,6H2/t7-,8+,9?,10?/m0/s1

InChI 密鑰

HECLRDQVFMWTQS-AFWXGSBKSA-N

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相关类别

一般說明

双环戊二烯（DCPD）是环戊二烯的二聚体，由两个不饱和双键组成（一个在降冰片烯环上，一个在环戊烯环上）。DCPT 可单独用于聚合物中，也可与其他碳氢化合物一起使用。它也用于制药、弹性体、聚碳酸酯和聚酯树脂。

應用

双环戊二烯可用于：
  • 采用 VARTM（真空辅助树脂转移模塑）工艺制备 CF/p-DCPD（碳纤维/聚双环戊二烯）复合材料。
  • 在 η5-环戊二烯基三（二甲基氨基）锆催化剂的制备中。
  • 在纤维素–马来酸酐–双环戊二烯共聚物基体的自由基聚合合成中。

特點和優勢

DCPD 与邻苯二甲酸和间苯二甲酸聚酯相比具有以下优点：
  • 低收缩率
  • 降低成本效益
  • 减少苯乙烯的排放
  • 薄层快速固化

訊號詞

Danger

危險分類

Acute Tox. 2 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

3 - Flammable liquids

水污染物質分類（WGK）

WGK 3

閃點（°F）

89.6 °F - closed cup

閃點（°C）

32 °C - closed cup

個人防護裝備

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Frontal ring-opening metathesis polymerization of dicyclopentadiene.
Mariani A, et al.
Macromolecules, 34(19), 6539-6541 (2001)
Sebastijan Kovačič et al.
ACS applied materials & interfaces, 6(21), 19075-19081 (2014-10-22)
Zinc(II) oxide nanoparticles were used for the stabilization of dicyclopentadiene (DCPD)-water-based high internal phase emulsions (HIPEs), which were subsequently cured using ring-opening metathesis polymerization (ROMP). The morphology of the resulting ZnO-pDCPD nanocomposite foams was investigated in correlation to the nanoparticle
Morphological and mechanical evaluation of hybrid organic-inorganic thermoset copolymers of dicyclopentadiene and mono-or tris (norbornenyl)-substituted polyhedral oligomeric silsesquioxanes.
Constable GS, et al.
Macromolecules, 37(4), 1276-1282 (2004)
Anna Kozłowska et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 20(43), 14120-14125 (2014-09-11)
Cyclic Ru-phenolates were synthesized, and these compounds were used as olefin metathesis catalysts. Investigation of their catalytic activity pointed out that, after activation with chemical agents, these catalysts promote ring-closing metathesis (RCM), enyne and cross-metathesis (CM) reactions, including butenolysis, with
Andre H St Amant et al.
Journal of the American Chemical Society, 141(34), 13619-13624 (2019-08-08)
Herein, we report the development of a scalable and synthetically robust building block based on norbornadiene (NBD) that can be broadly incorporated into a variety of macromolecular architectures using traditional living polymerization techniques. By taking advantage of a selective and
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