3006-93-7

  • Product Name:N,N'-1,3-Phenylene bismaleimide
  • Molecular Formula:C14H8N2O4
  • Purity:99%
  • Molecular Weight:
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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

maleic anhydride
108-31-6

maleic anhydride

magnesium(II) acetate tetrahydrate
16674-78-5

magnesium(II) acetate tetrahydrate

N,N'-(1,3-phenylene)dimaleimide
3006-93-7

N,N'-(1,3-phenylene)dimaleimide

Conditions
Conditions Yield
With acetic anhydride; In water; acetone;
84%
maleic anhydride
108-31-6

maleic anhydride

m-phenylenediamine
108-45-2,64554-26-3,76583-20-5

m-phenylenediamine

N,N'-(1,3-phenylene)dimaleimide
3006-93-7

N,N'-(1,3-phenylene)dimaleimide

Conditions
Conditions Yield
In ethyl acetate; toluene; at 60 ℃; for 5h; Time; Temperature;
 

3006-93-7 Upstream products

  • 108-31-6
    108-31-6

    maleic anhydride

  • 16674-78-5
    16674-78-5

    magnesium(II) acetate tetrahydrate

  • 108-45-2
    108-45-2

    m-phenylenediamine

  • 13161-99-4
    13161-99-4

    S01819

3006-93-7 Downstream products

  • 113452-03-2
    113452-03-2

    C36H24N2O6

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