Azobis(isobutyronitrile) | Solubility of Things

Identification

Molecular formula

C₈H₁₂N₄

CAS number

78-67-1

IUPAC name

1,1'-(Diazene-1,2-diyl)dibicyclo[4.3.0]nonane

State

At room temperature, azobis(isobutyronitrile) is typically found in a solid state. It is relatively stable under normal conditions, but may decompose when heated or exposed to strong light sources, releasing nitrogen gas and leaving behind active radicals.

Melting point (Celsius)

103.50

Melting point (Kelvin)

376.65

Boiling point (Celsius)

203.00

Boiling point (Kelvin)

476.15

General information

Molecular weight

164.21g/mol

Molar mass

164.2100g/mol

Density

1.1000g/cm³

Appearence

Azobis(isobutyronitrile) appears as a white crystalline solid. It is widely used as a radical initiator in various polymerization processes. The appearance may vary slightly depending on purity and particle size.

Comment on solubility

Solubility of 1,1'-(Diazene-1,2-diyl)dibicyclo[4.3.0]nonane

The solubility of 1,1'-(Diazene-1,2-diyl)dibicyclo[4.3.0]nonane is an intriguing topic due to its unique structure and functional groups. Generally speaking, the solubility of organic compounds like this one can be influenced by several factors:

Polarity: The presence of polar or nonpolar groups can affect solubility in various solvents. This compound, with its bicyclic structure, may exhibit distinct properties depending on the specific environment.
Hydrogen Bonding: The ability to form hydrogen bonds can enhance solubility in polar solvents, whereas nonpolar solvents may not effectively dissolve the compound.
Temperature: Increasing temperature often leads to greater solubility as kinetic energy enhances molecular movement.

In general, while precise solubility data for 1,1'-(Diazene-1,2-diyl)dibicyclo[4.3.0]nonane may not be widely documented, understanding its potential solubility involves considering:

Solvent compatibility: It may be soluble in organic solvents such as acetone or ethyl acetate.
Reactivity: Interaction with solvents could lead to potential reactions, impacting observed solubility.

As a final note, understanding the nuances of solubility for such compounds can lead to broader insights into their chemical behavior and applications. Always refer to specific experimental data for accurate assessments!

Interesting facts

Interesting Facts about 1,1'-(Diazene-1,2-diyl)dibicyclo[4.3.0]nonane

1,1'-(Diazene-1,2-diyl)dibicyclo[4.3.0]nonane is a fascinating compound that showcases the intriguing world of bicyclic structures and diazenes. Here are some captivating aspects of this compound:

Bicyclic Structure: This compound features a bicyclic structure, which consists of two interconnected rings. It exhibits unique geometric and electronic properties due to the constraint introduced by the cycles.
Diazene Functionality: The presence of diazene (N=N) within the structure influences its reactivity. Diazene compounds are known for their ability to undergo various chemical transformations, including polymerization and rearrangement reactions.
Potential Applications: Compounds like 1,1'-(Diazene-1,2-diyl)dibicyclo[4.3.0]nonane have potential applications in materials science, particularly in developing new polymers and conducting materials.
Research Interest: This compound motivates ongoing research in understanding its properties and how subtle changes in its structure can lead to significant effects on its behavior in reactions.
Synthetic Strategy: The synthesis of such bicyclic diazenes often involves intricate multi-step methodologies, showcasing the creativity and precision required in synthetic organic chemistry.

The study of 1,1'-(Diazene-1,2-diyl)dibicyclo[4.3.0]nonane inspires chemists to explore the diverse realms of chemical bonding and compound formation. As researchers delve deeper, they uncover the myriad of reactions and potential utilities hidden within this compound's unique structure.

Synonyms

DICYCLOHEXYLCARBODIIMIDE

N,N'-Dicyclohexylcarbodiimide

1,3-Dicyclohexylcarbodiimide

Cyclohexanamine, N,N'-methanetetraylbis-

dicyclohexylmethanediimine

Dicyclohexyl-Carbodiimide

NSC 30022

CHEBI:53090

EINECS 208-704-1

BRN 0610662

CCRIS 9266

DTXSID1023817

AI3-08191

HSDB 8049

UNII-0T1427205E

NSC-30022

NSC-53373

NSC-57182

1,3dicyclohexylcarbodiimide

N,N'dicyclohexylcarbodiimide

Cyclohexaamine, N,N'-methanetetraylbis-

DTXCID003817

CARBODIIMIDE,DICYCLOHEXYL

0T1427205E

EC 208-704-1

4-12-00-00072 (Beilstein Handbook Reference)

Methanediimine, N,N'-dicyclohexyl-

DICYCLOHEXYLCARBODIIMIDE [MI]

DICYCLOHEXYLCARBODIIMIDE [HSDB]

DICYCLOCARBODIIMIDE

Carbodiimide, dicyclohexyl

N,N'Methanetetraylbiscyclohexaamine

Cyclohexaamine, N,N'methanetetraylbis

Cyclohexanamine, N,N'methanetetraylbis

N,N'-Meth-anetetraylbiscyclohexanamine

Cyclohexaamine, N,N'methanetetraylbis (9CI)

Cyclohexaamine, N,N'-methanetetraylbis-(9CI)

208-704-1

inchi=1/c13h22n2/c1-3-7-12(8-4-1)14-11-15-13-9-5-2-6-10-13/h12-13h,1-10h

qossaotznidxma-uhfffaoysa-n

538-75-0

DCCD

DCCI

n,n-dicyclohexylcarbodiimide

Carbodicyclohexylimide

Bis(cyclohexyl)carbodiimide

DCC

n,n'-methanediylidenedicyclohexanamine

Carbodiimide, dicyclohexyl-

Dicylcohexylcarbodiimide

DCC Crosslinker

N,N'-Methanetetraylbiscyclohexaamine

N,N'-dicyclohexylmethanediimine

N,N-dicyclohexylcarbodiimide(DCC)

dicyclohexyl carbodiimide

C13H22N2

MFCD00011659

Cyclohexanamine,N'-methanetetraylbis-

N,N'-Dicyclohexylcarbodiimide (DCC)

CAS-538-75-0

Dicyclimide;1,3-dicyclohexylcarbodiimide;N,N-Dicyclohexylcarbodiimide;N,N'-Methanediylidenedicyclohexanamine

n,n'-dicyclohexylcarbodiimid

N,N'-dicyclohexylcarbodimide

N,N'-DICYCLOHEXYL-CARBODIIMIDE

dicyclohexylcarbodiimid

dicyclohexylcarbodimide

dicylohexylcarbodiimide

Dicylcohexylcarbodimide

dicyciohexylcarbodiimide

Dicyclohexyicarbodiimide

dicyclohexyl carbodimide

dicylohexyl-carbodiimide

dicyclo-hexylcarbodiimide

dicyclohe-xylcarbodiimide

dicyclohexylcarbo-diimide

dicyclohexylcarbod iimide

dicyclohexylcarbodi-imide

Dicyclohexyl carbo diimide

Dicyclohexyl-carboxydilmide

SCHEMBL303

Epitope ID:114067

1,3-dicyclohexylcarbodiimid

1,3-dicyclohexylcarbodimide

1.3-dicyclohexylcarbodimide

n,n'-dicylohexylcarbodiimide

1,3-dicylcohexylcarbodiimide

1.3-dicyclohexylcarbodiimide

N, N'dicyclohexylcarbodimide

1,N'-dicyclohexylcarbodimide

n.n'-dicyclohexylcarbodiimide

N,N'-dicylcohexylcarbodiimide

1, 3-dicyclohexylcarbodiimide

1,3- dicyclohexylcarbodiimide

1,3-dicyclo-hexylcarbodiimide

1,3-dicyclohexyl carbodiimide

1,3-dicyclohexyl-carbodiimide

1,3-dicyclohexylcarbo-diimide

N, N'-dicyclohexylcarbodimide

N,N'-Dicyclohexyl carbodimide

n,n'-dicyclohexyl carbodiimide

N, N'-dicyclohexylcarbodiimide

N,N'-dicyclo hexylcarbodiimide

N,N'-dicyclo-hexylcarbodiimide

1,3-di-cyclohexyl carbodiimide

1,3-dicyclo hexyl carbodiimide

1,3-dicyclohexyl carbo-diimide

1,3-dicyclohexyl- carbodiimide

CHEMBL162598

N,N,-dichyclohexyl-carbodiimide

N, N'-dicyclohexyl carbodiimide

N,N'- dicyclohexyl carbodiimide

N,N'-dicyclo hexyl carbodiimide

N.N' - dicyclohexylcarbodiimide

BDBM129231

DCC, 99%

HY-Y1092

NSC30022

NSC53373

NSC57182

DCC, 1.0 M in methylene chloride

Tox21_203000

Tox21_303237

BBL012208

N,N'-Methanetetraylbiscyclohexanamine

STL089892

AKOS000120067

US8815951, dicyclohexylcarbodiimide

CS-W020097

FD05508

N,N'-methanediylidene-dicyclohexanamine

US8815951, N/A

DCC, puriss., >=99.0% (GC)

NCGC00091497-01

NCGC00091497-02

NCGC00091497-03

NCGC00091497-04

NCGC00257167-01

NCGC00260545-01

BP-13398

DB-002694

N-(N-cyclohexylcarboximidoyl)cyclohexanamine

D0436

D0437

N-((cyclohexylimino)methylene)cyclohexanamine

NS00003057

EN300-20280

N-((cyclohexylimino)methylene) cyclohexanamine

C93487

Q306565

1,3-Dicyclohexylcarbodiimide solution (50% in THF)

N,N inverted exclamation marka-Dicyclohexylcarbodiimide

F0001-1397

Z104477564

1,3-Dicyclohexyl carbodiimide;N,N'-Dicyclohexylcarbodiimide

1,3-Dicyclohexylcarbodiimide solution (1.0 M in methylene chloride)