Interesting facts
Interesting Facts about 1,2-Diphenylguanidine
1,2-Diphenylguanidine is a fascinating organic compound with a range of applications in chemistry and materials science. Here are some intriguing aspects of this compound:
- Structure and Isomerism: The compound showcases a unique molecular structure due to the presence of two phenyl groups attached to the guanidine backbone. This arrangement allows for interesting isomeric possibilities, influencing its physical and chemical properties.
- Role in Polymer Chemistry: 1,2-Diphenylguanidine is extensively used as an accelerator in the curing process of rubber. This helps in enhancing the elasticity and durability of rubber products, making it a vital component in the tire industry and various elastomer formulations.
- Thermal Stability: One of the noteworthy qualities of 1,2-diphenylguanidine is its excellent thermal stability. This characteristic is crucial for applications in high-temperature environments, ensuring that the compound maintains its effectiveness and does not decompose easily.
- Biological Considerations: Studies have investigated the potential biological activities of this compound. Some research suggests that it might interact with biological systems, prompting a deeper exploration into its toxicity and safety profile for various applications.
- Interesting Applications: Beyond its use in rubber, 1,2-diphenylguanidine serves in the synthesis of other chemical compounds and as a catalyst in certain chemical reactions, showcasing its versatility in organic synthesis.
In conclusion, 1,2-diphenylguanidine represents a compelling subject for further study and application across various fields. Its structural peculiarities and functional roles in industry make it an essential compound in both academic research and industrial processes.
Synonyms
1,3-Diphenylguanidine
102-06-7
Diphenylguanidine
N,N'-DIPHENYLGUANIDINE
1,2-diphenylguanidine
Vulkazit
Accelerator D
Nocceler D
Melaniline
s-Diphenylguanidine
Denax
Vulkacite D
Vulkacit D
Vulcafor DPG
Guanidine, N,N'-diphenyl-
DPG accelerator
diphenyl guanidine
Vulkacit D/C
Denax DPG
1,3-Difenylguanid
Guanidine, 1,3-diphenyl-
Sanceler D
Dwufenyloguanidyna
Soxinol D
USAF EK-1270
Vanax DPG
USAF B-19
CCRIS 1395
HSDB 5345
DPG vulcanizer
UNII-6MRZ85RNHQ
Vulcacid D
NCI-C60924
Akrochem DPG
Perkacit DPG
Vulcaid DPG
NSC 3272
EINECS 203-002-1
MFCD00001758
DTXSID3025178
AI3-00225
NSC-3272
6MRZ85RNHQ
D.P.G
CHEMBL77675
DTXCID005178
DFG
CHEBI:144319
EC 203-002-1
1,3-DIPHENYLGUANIDINE [MI]
N,N'-DIPHENYLGUANIDINE [HSDB]
NCGC00090698-02
NCGC00090698-04
Sym-diphenylguanidine
DPG (VAN)
Dwufenyloguanidyna [Polish]
1,3-Difenylguanid [Czech]
CAS-102-06-7
SMR000567260
phenax
sDiphenylguanidine
diphenyl-guanidine
1,3Difenylguanid
[imino(phenylamino)methyl]phenylamine
CHLOROSTAIN BR
RHENOGRAN DPG
PERKACIT DP
Guanidine,3-diphenyl-
Guanidine,N'-diphenyl-
ACCEL DM-R
Guanidine, 1,3diphenyl
Guanidine, N,N'diphenyl
N,N'-Diphenyl-guanidine
Maybridge1_002607
N,N''-Diphenyl-guanidine
WLN: MUYMR & MR
Cambridge id 5539652
REGID_for_CID_7594
SCHEMBL35172
MLS001055401
MLS001181565
DivK1c_001359
1,3-Diphenylguanidine, 97%
Accelerator D Diphenyl guanidine
HMS548O11
NSC3272
1,3-Diphenylguanidine (Standard)
HMS2870H09
HY-W014332R
Tox21_110998
Tox21_400041
BBL011030
BDBM50010769
CCG-49163
STK802182
STL301515
AKOS000118775
AKOS022133740
Tox21_110998_1
CS-W015048
DB14191
HY-W014332
1,3-Diphenylguanidine, primary standard
CDS1_000319
NCGC00090698-01
NCGC00090698-03
NCGC00090698-05
NCGC00090698-06
DA-16706
VS-02813
D0723
D0892
NS00011462
EN300-21474
D88181
SBI-0653925.0001
AE-641/01188002
Q2537147
SR-01000638639-1
BRD-K12362304-001-07-3
F3096-1727
Z203045076
1,3-Diphenylguanidine, analytical standard (for titrimetry)
Solubility of 1,2-Diphenylguanidine
1,2-diphenylguanidine, known for its unique structure and chemical properties, exhibits intriguing solubility characteristics. Here are the key points to consider:
To summarize, the solubility behavior of 1,2-diphenylguanidine emphasizes the importance of solvent type and temperature in determining its environmental interactions and applications. This compound’s solubility landscape is a clear reminder of the intricate nature of chemical compounds in different solutions: