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3,4,5-Trimethoxyaniline

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Identification
Molecular formula
C9H13NO3
CAS number
24329-25-9
IUPAC name
3,4,5-trimethoxyaniline
State
State

At room temperature, 3,4,5-trimethoxyaniline is in a solid state. It typically presents as a crystalline powder, suitable for various chemical applications in solid form.

Melting point (Celsius)
60.00
Melting point (Kelvin)
333.15
Boiling point (Celsius)
163.00
Boiling point (Kelvin)
436.15
General information
Molecular weight
183.20g/mol
Molar mass
183.2020g/mol
Density
1.1690g/cm3
Appearence

3,4,5-Trimethoxyaniline is a pale yellow to tan crystalline solid. It can appear as a powder or as finely divided crystals.

Comment on solubility

Solubility of 3,4,5-trimethoxyaniline

3,4,5-trimethoxyaniline, known for its unique structure with three methoxy groups attached to the aniline ring, exhibits interesting solubility characteristics. Understanding its solubility is crucial for its applications in various chemical processes.

Key Points on Solubility:

  • Solvent Interaction: 3,4,5-trimethoxyaniline is generally more soluble in organic solvents due to the presence of the methoxy groups, which enhance its hydrophobic interactions.
  • Polarity Effect: The methoxy groups are electron-donating, influencing the overall polarity of the compound and resulting in varying solubility in polar and non-polar solvents.
  • Temperature Influence: As with many organic compounds, increasing temperature typically enhances solubility, allowing for better dissolution in appropriate solvents.

In summary, while 3,4,5-trimethoxyaniline is primarily soluble in organic solvents like ethanol and acetone, its solubility may be influenced by several factors including solvent choice, temperature, and the presence of other solutes. Exploring these interactions can yield insights into optimizing its use in chemical applications.

Interesting facts

Interesting Facts about 3,4,5-Trimethoxyaniline

3,4,5-Trimethoxyaniline, often abbreviated as TMA, is a fascinating compound with several intriguing properties and applications. This organic compound belongs to the class of anilines, which are basic derivatives of aromatic amines. Here are some noteworthy aspects of 3,4,5-trimethoxyaniline:

  • Chemical Structure: TMA features a benzene ring substituted with three methoxy groups and an amino group. This unique arrangement plays a crucial role in its reactivity and functionality.
  • Applications: Due to its chemical structure, TMA is often utilized in the production of dyes, pigments, and polymers. Its vibrant coloration makes it a popular choice in textile and paint industries.
  • Role as an Intermediate: TMA serves as an important intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its versatility allows chemists to modify its structure for targeted applications.
  • Biological Activity: Research indicates that compounds related to TMA may exhibit biological activity, including potential antimicrobial and anticancer properties. This opens up avenues for further exploration in medicinal chemistry.
  • Research Interest: The compound has drawn attention in the field of materials science, where it is studied for its electrical and optical properties. Such research contributes to advancements in electronic devices and sensors.

As a chemist or a chemistry student, understanding 3,4,5-trimethoxyaniline could spark inspiration for innovative research and applications. Its blend of functionality and versatility makes it a notable compound in organic chemistry.

Synonyms
3,4,5-TRIMETHOXYANILINE
24313-88-0
Benzenamine, 3,4,5-trimethoxy-
Aniline, 3,4,5-trimethoxy-
EINECS 246-154-4
NSC 37006
AI3-52691
DTXSID8066979
RefChem:90930
DTXCID7037058
246-154-4
InChI=1/C9H13NO3/c1-11-7-4-6(10)5-8(12-2)9(7)13-3/h4-5H,10H2,1-3H
XEFRNCLPPFDWAC-UHFFFAOYSA-N
3,4,5-trimethoxybenzenamine
3,4,5-trimethoxy aniline
MFCD00008393
3,4,5-trimethoxy-phenylamine
3,4,5-trimethoxyphenylamine
[3,4,5-tris(methyloxy)phenyl]amine
NSC-37006
NSC37006
3,5-Trimethoxyaniline
3,4,5-trimethoxyanilin
WJM47ZMQ5S
3,4,5-trimethoxy-aniline
3, 4, 5-trimethoxyaniline
Benzenamine,4,5-trimethoxy-
SCHEMBL191996
3, 4, 5-trimethoxy aniline
3,4,5-Trimethoxy Phenylamine
3,4,5-tris(methyloxy)aniline
orb2939784
SCHEMBL1806447
(3,4,5-trimethoxyphenyl)amine
CHEMBL3814177
WLZ3742
3,4,5-Trimethoxyaniline, 97%
HMS1776M14
3,4,5-tris(methyloxy)phenyl amine
BCP22445
1-(3,4,5-Trimethoxyphenyl)aniline
BBL010288
SBB072154
STK506779
AKOS000118847
CS-W007860
DS-2261
FT28523
HY-W007860
PS-5888
SB10520
PD210469
DB-046393
NS00027612
ST45027587
T1055
EN300-18969
A817216
F008860
F2190-0522
Z104341510
3,4,5-Trimethoxybenzenamine;3,4,5-Trimethoxyphenylamine;3,4,5-Tris(methyloxy)aniline