CAS 4856-87-5

1,6-Bismaleimidohexane

Description:

1,6-Bismaleimidohexane, with the CAS number 4856-87-5, is an organic compound characterized by its structure, which features two maleimide groups attached to a hexane backbone. This compound is typically used in the synthesis of thermosetting resins and polymers due to its ability to undergo cross-linking reactions when heated or cured with suitable hardeners. It exhibits good thermal stability and chemical resistance, making it suitable for high-performance applications in industries such as aerospace, automotive, and electronics. The presence of maleimide groups allows for the formation of strong covalent bonds, enhancing the mechanical properties of the resulting materials. Additionally, 1,6-Bismaleimidohexane is often utilized in composite materials, where it contributes to improved adhesion and durability. Its handling requires caution, as it may pose health risks if inhaled or ingested, necessitating appropriate safety measures during use. Overall, this compound is valued for its versatility and effectiveness in advanced material applications.

Formula: C₁₄H₁₆N₂O₄

InChI: InChI=1/C14H16N2O4/c17-11-5-6-12(18)15(11)9-3-1-2-4-10-16-13(19)7-8-14(16)20/h5-8H,1-4,9-10H2

InChI key: InChIKey=PYVHLZLQVWXBDZ-UHFFFAOYSA-N

SMILES: C(CCCCCN1C(=O)C=CC1=O)N2C(=O)C=CC2=O

Synonyms:

• 1,1'-(Hexane-1,6-diyl)bis-1H-pyrrole-2,5-dione
• 1,1′-(1,6-Hexanediyl)bis[1H-pyrrole-2,5-dione]
• 1,1′-hexane-1,6-diylbis(1H-pyrrole-2,5-dione)
• 1,6-Bismaleimidehexane
• 1,6-Bismaleimidohexane
• 1,6-Bmh
• 1,6-Dimaleimidohexane
• 1,6-Hexamethylenebis[maleimide]
• 1,6-Hexanediylbismaleimide
• 1,6-Maleimidohexane
• 1-[6-(2,5-Dioxopyrrol-1-yl)hexyl]pyrrole-2,5-dione
• 1H-Pyrrole-2,5-dione, 1,1'-(1,6-hexanediyl)bis-
• 1H-Pyrrole-2,5-dione, 1,1'-(1,6-hexanediyl)bis- (9CI)
• Ai3-51359
• BMH Crosslinker
• Brn 0253749
• Gmbmi
• Gp 207R
• Hexamethylenediamine bismaleimide
• Maleimide, N,N'-hexamethylenedi-
• N,N'-Hexamethylenebis(maleimide)
• N,N'-Hexamethylenedimaleimide
• Nsc 12818
• 4-21-00-04640 (Beilstein Handbook Reference)
• N,N'-(Hexane-1,6-diyl)dimaleimide
• 1,6-Bis(maleimido)hexane &gt
• HEXYLDIMALEIMIDE
• N,N'-Hexamethylenebismaleimide
• BIS-MALEIMIDOHEXANE
• BMH
• 1,1’-(1,6-hexanediyl)bis-1h-pyrrole-5-dione
• N,N'-(1,6-Hexanediyl)di(maleimide)
• Hmdm
• 1-(6-maleimidohexyl)-3-pyrroline-2,5-quinone
• n,n’-hexamethylenedi-maleimid
• BMH (bismaleimidohexane)
• 1,6-Bis(maleimide)hexane
• 1,6-BISMALEIMIDOHEXANE 96+%
• 1,6-Di(maleimido)hexane
• 1,6-HEXANE DIMALEIMIDE
• N,N'-HEXAMETHYLENEBISMALEIMIDE
• N,N'-(1,6-Hexanediyl)bis(maleimide)

1,6-Bis(maleimido)hexane

CAS: 4856-87-5

Formula: C₁₄H₁₆N₂O₄

Purity: >97.0%(HPLC)(N)

Color and Shape: White to Almost white powder to crystal

Molecular weight: 276.29

Ref: 3B-B1787

1,6-Bismaleimidohexane, 97%

CAS: 4856-87-5

A sulfhydryl reactive homobifunctional cross linking reagent. Under mild conditions, will permit irreversible cross-linking of sulfhydral containing compounds at a pH range of 6.5 to 7.5. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some doc

Formula: C₁₄H₁₆N₂O₄

Purity: 97%

Molecular weight: 276.29

Ref: 02-H58874

1,1'-(Hexane-1,6-diyl)bis(1H-pyrrole-2,5-dione)

CAS: 4856-87-5

Formula: C₁₄H₁₆N₂O₄

Purity: 97%

Color and Shape: Solid

Molecular weight: 276.2878

Ref: IN-DA003DR3

1,1’-(Hexane-1,6-Diyl)Bis(1H-Pyrrole-2,5-Dione)

CAS: 4856-87-5

1,1’-(Hexane-1,6-Diyl)Bis(1H-Pyrrole-2,5-Dione)

Purity: 97%

Molecular weight: 276.29g/mol

Ref: 54-OR1009024

1,6-BISMALEIMIDOHEXANE

CAS: 4856-87-5

Formula: C₁₄H₁₆N₂O₄

Purity: 98%

Molecular weight: 276.292

Ref: 10-F471319