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Ametoctradin

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Identification
Molecular formula
C18H15N5
CAS number
865318-97-4
IUPAC name
6-phenyl-1,3,5-triazine-2,4-diamine
State
State

Ametoctradin is typically a solid at room temperature, often in a crystalline form, and is used primarily as a fungicide in the agricultural industry.

Melting point (Celsius)
173.20
Melting point (Kelvin)
446.35
Boiling point (Celsius)
265.50
Boiling point (Kelvin)
538.65
General information
Molecular weight
303.33g/mol
Molar mass
303.3310g/mol
Density
1.3400g/cm3
Appearence

Ametoctradin appears as a light brown to brown solid or powder. It is usually provided in technical-grade form for utilization in various applications.

Comment on solubility

Solubility of 6-phenyl-1,3,5-triazine-2,4-diamine

The solubility of 6-phenyl-1,3,5-triazine-2,4-diamine can be an intriguing subject due to its unique molecular structure and potential applications.

This compound displays a moderate solubility in various solvents, influenced by its chemical characteristics:

  • Polarity: The presence of amino groups (-NH2) contributes to its polarity, which generally increases solubility in polar solvents like water.
  • Hydrogen bonding: The amino groups can form hydrogen bonds, enhancing solubility in protic solvents.
  • Solvent interactions: It may find better solubility in organic solvents such as ethanol and dimethyl sulfoxide (DMSO), where interactions with the solvent can overcome the inherent structural stability.

In summary, the solubility pattern of 6-phenyl-1,3,5-triazine-2,4-diamine is governed by its molecular attributes and environmental conditions, making it an interesting subject for further study:

  1. Preferred in polar solvents
  2. Enhanced interactions via hydrogen bonding
  3. Varies significantly with temperature and concentration

Understanding these solubility principles is crucial for its practical applications in chemical and pharmaceutical contexts.

Interesting facts

Interesting Facts About 6-Phenyl-1,3,5-triazine-2,4-diamine

6-Phenyl-1,3,5-triazine-2,4-diamine, often abbreviated as PTDA, is a fascinating compound in the realm of organic chemistry. Its unique structure consists of a triazine ring, which is an aromatic heterocycle made up of three nitrogen atoms and three carbon atoms. This compound has garnered attention in various fields due to its remarkable properties and applications.

Key Features

  • Versatile Applications: PTDA is widely studied for its potential use in organic electronics, particularly in the development of dyes and pigments. Its triazine structure allows for various substitutions that can modify its electronic properties, making it useful in materials science.
  • Biological Significance: Research has indicated that compounds similar to PTDA possess bioactivity, including antimicrobial and antitumor effects. This raises intriguing possibilities for its application in pharmaceuticals and agrochemicals.
  • Synthetic Pathways: The synthesis of PTDA can involve multiple approaches, including reactions starting from easily accessible precursors. Such synthetic versatility often prompts chemists to explore more efficient methods for large-scale production.
  • Environmental Impact: Investigating the environmental fate of triazine compounds, including PTDA, is important. Understanding their breakdown and interaction with biological systems can guide the development of safer chemicals with low ecological footprints.

In the words of a prominent chemist, "The beauty of chemistry lies not only in its complexity but also in the endless possibilities derived from even the simplest structures."
Exploring compounds like 6-Phenyl-1,3,5-triazine-2,4-diamine exemplifies this notion, as it showcases the interplay between structure, function, and utility in modern chemistry.

Explore Further

Students and researchers alike are encouraged to delve deeper into the properties and potential of PTDA, as its diverse applications might pave the way for innovative solutions in technology and medicine. By understanding the underlying principles of its reactivity and functionality, we can unlock new avenues for research and development.

Synonyms
Benzoguanamine
91-76-9
6-Phenyl-1,3,5-triazine-2,4-diamine
2,4-DIAMINO-6-PHENYL-1,3,5-TRIAZINE
Benzoguanimine
1,3,5-Triazine-2,4-diamine, 6-phenyl-
USAF RH-5
2,4-Diamino-6-phenyl-s-triazine
2-Phenyl-4,6-diamino-s-triazine
4,6-Diamino-2-phenyl-s-triazine
Benzoguanamine (VAN)
ENT 60118
s-Triazine, 2,4-diamino-6-phenyl-
6-Phenyl-1,3,5-triazine-2,4-diyldiamine
2-Phenyl-4,6-diamino-1,3,5-triazine
NSC 3267
CCRIS 9098
DTXSID1020142
HSDB 5275
B9E2Q3VTUB
EINECS 202-095-6
BRN 0153223
6-Phenyl-[1,3,5]triazine-2,4-diamine
AI3-22162
1,3,5-Triazine, 2,4-diamino-6-phenyl-
NSC-3267
BENZOGUANAMINE [MI]
DTXCID50142
EC 202-095-6
4-26-00-01244 (Beilstein Handbook Reference)
2,6-Diamino-4-phenyl-1,3,5-triazine
2,4-DIAMINO-6-PHENYL-1,3,5-TRIAZINE [HSDB]
CAS-91-76-9
SMR000059313
UNII-B9E2Q3VTUB
BZE
MFCD00023187
2,4Diamino6phenylstriazine
2Phenyl4,6diaminostriazine
4,6Diamino2phenylstriazine
Cambridge id 5109426
SCHEMBL27898
2-Phenyl-4,3,5-triazine
BENZOGUANAMINE [INCI]
MLS000079044
MLS002207438
BIDD:GT0824
sTriazine, 2,4diamino6phenyl
CHEMBL337319
s-Triazine,4-diamino-6-phenyl-
NSC3267
2Phenyl4,6diamino1,3,5triazine
6Phenyl1,3,5triazine2,4diamine
HMS1607F08
HMS2224A20
HMS3357J18
WLN: T6N CN ENJ BZ DZ FR
Tox21_201624
Tox21_302969
1,3,5Triazine, 2,4diamino6phenyl
1,3,5Triazine2,4diamine, 6phenyl
BBL008203
BDBM50595380
CCG-15318
STK803078
STK832888
AKOS000120882
AKOS005623544
AS-5489
CS-W015988
1,5-Triazine-2,4-diamine, 6-phenyl-
6-phenyl-2,4-diamino-1,3,5-triazine
NCGC00064041-03
NCGC00064041-04
NCGC00256484-01
NCGC00259173-01
AC-22494
D0111
EU-0067360
NS00005541
EN300-16709
2,4-Diamino-6-phenyl-1,3,5-triazine, 97%
E83015
(4-amino-6-phenyl-[1,3,5]triazin-2-yl)-amine
AG-690/36704015
SR-01000393559
SR-01000393559-1
Benzoguanamine;2,4-Diamino-6-phenyl-1,3,5-triazine;
Q27274545
Z56756414
4-imino-6-phenyl-4,5-dihydro-1,3,5-triazin-2-amine
4-imino-6-phenyl-4,5-dihydro-1,3,5-triazin-2-ylamine
Benzoguanamine// 6-Phenyl-1,3,5-triazine-2,4-diamine
202-095-6