3006-93-7
- Product Name:N,N'-1,3-Phenylene bismaleimide
- Molecular Formula:C14H8N2O4
- Purity:99%
- Molecular Weight:
Product Details;
CasNo: 3006-93-7
Molecular Formula: C14H8N2O4
Appearance: yellow crystalline powder
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3006-93-7 Chemical & Physical Properties |
|
Melting point |
198-201 °C(lit.) |
Boiling point |
499.3±28.0 °C at 760 mmHg |
Density |
1.6±0.1 g/cm3 |
Molecular Formula |
C14H8N2O4 |
Molecular Weight |
268.224 |
Flash Point |
250.7±16.4 °C |
PSA |
74.76000 |
LogP |
-0.04 |
Exact Mass |
268.048401 |
form |
powder to crystal |
color |
Light yellow to Brown to Dark green |
Vapour Pressure |
0.0±1.3 mmHg at 25°C |
Index of Refraction |
1.704 |
Water Solubility |
negligible soluble |
storage temp. |
Sealed in dry,Room Temperature |
Good Manufacturer Export High Purity N,N'-1,3-Phenylene bismaleimide
N,N'-1,3-Phenylene bismaleimide is yellow crystalline powder, which used as rubber vulcanizing agent, rubber crosslinkimg agent. N,N'-1,3-Phenylene bismaleimide and sulfur coordination to prevent reversion to improve the heat resistance, reduce heat, anti-aging, improve adhesion of the rubber and tire cord and vulcanized rubber modulus. In the case of N,N′-(1,3-phenylene)bismaleimide (BMIR), the molecule is more rigid due to the presence of a single aromatic ring between both sides containing the functional alkene group.
Isomeric SMILES: C1=CC(=CC(=C1)N2C(=O)C=CC2=O)N3C(=O)C=CC3=O
InChIKey: IPJGAEWUPXWFPL-UHFFFAOYSA-N
InChI: InChI=1S/C14H8N2O4/c17-11-4-5-12(18)15(11)9-2-1-3-10(8-9)16-13(19)6-7-14(16)20/h1-8H
3006-93-7 Relevant articles
Synthesis and antioxidation behavior in EPDM of novel macromolecular antioxidants with crosslinking and antioxidation effects
Qingkun Liu a b, Peng Wei a b, Chuanbo Cong a b, Xiaoyu Meng a b, Qiong Zhou a b
Polymer Degradation and Stability Volume 205, November 2022, 110155
A novel antioxidant denoted as HVA-2@MB was synthesized through the reaction of N,N'-1,3-phenylene bismaleimide (HVA-2) and 2-mercaptobenzimidazole (MB) catalyzed by triethylamine.
Self-evolving materials based on metastable-to-stable crystal transition of a polymorphic polyolefin
Check for updates Wenhua Yuan, a Chengtao Yu,ab Shanshan Xu,a Lingling Ni,a Wenqing Xu,a Guorong Shan, ab Yongzhong Bao ab and Pengju Pan *ab
Materials Horizons, Issue 2, 2022
The commercialized PB was partially crosslinked by blending with dicumyl peroxide (DCP) and N,N′-1,3-phenylene bismaleimide (PM, Fig. S1, ESI†). DCP was used to initiate the free …
3006-93-7 Process route
- 108-31-6
maleic anhydride
- 16674-78-5
magnesium(II) acetate tetrahydrate
- 3006-93-7
N,N'-(1,3-phenylene)dimaleimide
Conditions | Yield |
---|---|
With acetic anhydride; In water; acetone;
|
84% |
- 108-31-6
maleic anhydride
- 108-45-2,64554-26-3,76583-20-5
m-phenylenediamine
- 3006-93-7
N,N'-(1,3-phenylene)dimaleimide
Conditions | Yield |
---|---|
In ethyl acetate; toluene; at 60 ℃; for 5h; Time; Temperature;
|
3006-93-7 Upstream products
-
108-31-6
maleic anhydride
-
16674-78-5
magnesium(II) acetate tetrahydrate
-
108-45-2
m-phenylenediamine
-
13161-99-4
S01819
3006-93-7 Downstream products
-
113452-03-2
C36H24N2O6
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