Interesting facts
Interesting Facts about 2,6-Diisopropylaniline
2,6-Diisopropylaniline is a fascinating compound with multiple applications and significance in various fields of chemistry and industry. Here are some interesting insights into this compound:
- Chemical Structure: 2,6-Diisopropylaniline features a benzene ring substituted by two isopropyl groups and an amino group, making it a member of the aniline family. This unique substitution pattern contributes to both its chemical properties and reactivity.
- Applications:
- It is commonly utilized as a precursor in the synthesis of dyes and pigments, highlighting its importance in the color industry.
- In the field of organic chemistry, it serves as an intermediate in the production of various chemical compounds, showcasing its versatility.
- Safety Precautions: As with many organic compounds, handling 2,6-diisopropylaniline requires proper safety measures. It is important to be aware of its potential health impacts and to follow appropriate protocols when working with it in the laboratory.
- Environmental Considerations: In studying this compound, chemists often consider its environmental impact, particularly in relation to its persistence and degradation in ecosystems.
In Conclusion
2,6-Diisopropylaniline not only plays a crucial role in industrial chemistry but also presents an interesting subject of study for students and researchers alike. Its unique structural features and diverse applications contribute to its significance in the compound library of organic chemistry.
Synonyms
2,6-DIISOPROPYLANILINE
24544-04-5
Benzenamine, 2,6-bis(1-methylethyl)-
diisopropylaniline
Aniline, 2,6-diisopropyl-
2,6-Diisopropyl aniline
2,6-Diisopropylphenylamine
2,6-Dilsopropylaniline
BRN 2208763
EINECS 246-305-4
DTXSID5022279
190BG0089I
DTXCID302279
EC 246-305-4
3-12-00-02764 (Beilstein Handbook Reference)
2,6diisopropyl aniline
2,6Diisopropylphenylamine
Aniline, 2,6diisopropyl
RefChem:587932
Benzenamine, 2,6bis(1methylethyl)
246-305-4
2,6-di(propan-2-yl)aniline
MFCD00008887
2,6-bis(propan-2-yl)aniline
2,6-bis(1-methylethyl)aniline
EN300-19395
UNII-190BG0089I
2,6-Diisopropyl- aniline; 2,6-Bis(1-methylethyl)aniline; 2,6-Bis(1-methylethyl)benzenamine; 2,6-Diisopropylphenylamine; N-(2,6-Diisopropylphenyl)amine
2,6-diisopropyaniline
2,6-diisoproylaniline
2,6 diisopropylaniline
2, 6-diisopropylaniline
2,6-diisopropyl-aniline
2,6-di-iso-propylaniline
2,6-diisopropyl-phenylamine
2,6-diisopropylphenyl-amine
(2,6-diisopropylphenyl)amine
2,6-diisopropyl-phenyl amine
SCHEMBL104314
SCHEMBL140786
2,6-Diisopropylaniline, 97%
orb2940294
SCHEMBL1807000
SCHEMBL6543970
2,6-bis(methylethyl)phenylamine
CHEMBL3183764
2,6-Diisopropylaniline (DIPA)
MSK1294
BDBM626075
BCP25856
Tox21_302145
BBL011276
STK940261
AKOS000118849
AC-4779
AT11199
CS-W017358
FD00540
HY-W016642
NCGC00255131-01
BP-21134
DS-12418
SY001946
CAS-24544-04-5
DB-002414
D1755
NS00005202
ST50406698
2,6-Diisopropylaniline, technical grade, 90%
2,6-Diisopropylaniline, technical, ~90% (GC)
F791468
Q27252049
F8881-7788
Z104473708
InChI=1/C12H19N/c1-8(2)10-6-5-7-11(9(3)4)12(10)13/h5-9H,13H2,1-4H
DIPA 2,6-DIISOPROPYLANILINE 2,6-bis(1-methylethyl)-benzenamin
Solubility of 2,6-Diisopropylaniline
2,6-Diisopropylaniline, with the chemical formula C13H19N, exhibits unique solubility characteristics that are noteworthy in both organic and industrial applications. This compound, belonging to the class of aromatic amines, can be described as partially soluble in water but demonstrates greater solubility in organic solvents.
Key Solubility Insights:
In summary, while 2,6-diisopropylaniline may present challenges for dissolution in polar solvents like water, its compatibility with non-polar solvents allows it to be effectively utilized in various chemical processes. As such, understanding its solubility is crucial for applications in synthesis and formulation.