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Triphenylmethanol

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Identification
Molecular formula
C19H16O
CAS number
76-84-6
IUPAC name
triphenylmethanol
State
State

At room temperature, triphenylmethanol is in a solid state. It is usually handled in the form of a powder or crystals.

Melting point (Celsius)
160.00
Melting point (Kelvin)
433.15
Boiling point (Celsius)
360.00
Boiling point (Kelvin)
633.15
General information
Molecular weight
260.33g/mol
Molar mass
260.3330g/mol
Density
1.1990g/cm3
Appearence

Triphenylmethanol is a white crystalline solid. It is known for its characteristic crystalline form and is often used in laboratories for various synthesis purposes.

Comment on solubility

Solubility of Triphenylmethanol

Triphenylmethanol, with the chemical formula C19H20O, exhibits unique solubility properties that can be intriguing when considering its application in various chemical processes. Here’s an overview of its solubility characteristics:

  • Solvent Compatibility: Triphenylmethanol is generally soluble in organic solvents such as ethanol, acetone, and chloroform, indicating its compatibility with nonpolar to moderately polar solvents.
  • Water Solubility: It demonstrates very poor solubility in water due to its nonpolar aromatic structure, which does not interact favorably with polar water molecules.
  • Molecular Structure Influence: The bulky phenyl groups hinder hydrogen bonding with water, further contributing to its limited aqueous solubility.

In summary, the solubility of triphenylmethanol highlights the interplay between its molecular structure and the properties of solvents, showcasing its preferential affinity for organic environments while remaining largely insoluble in water. As always in chemistry, understanding solubility is crucial for practical applications, from synthesis to formulation.

Interesting facts

Interesting Facts about Triphenylmethanol

Triphenylmethanol, an intriguing organic compound, is renowned for both its practical applications and unique properties. Here are some fascinating insights:

  • Versatile Solvent: Triphenylmethanol is often used as a solvent in organic synthesis due to its ability to dissolve a wide range of organic substances, making it an essential component in many laboratory procedures.
  • Color Indicator: It is sometimes utilized as a color indicator in chemical reactions, helping scientists to easily observe changes in reaction conditions.
  • Self-Disproportionation: This compound uniquely undergoes a self-disproportionation reaction, demonstrating multiple oxidation states. This characteristic can be utilized in various chemical synthesis pathways.
  • Polymorphic Forms: Triphenylmethanol can exist in multiple polymorphic forms, which can influence its physical and chemical behaviors — a fascinating area of study for material scientists.
  • Historical Significance: The compound has a rich history in the field of chemistry, often associated with the work of early organic chemists who explored its properties and applications in-depth.
  • Green Chemistry: Being non-toxic and less harmful to the environment, triphenylmethanol aligns well with the principles of green chemistry, promoting sustainable practices in chemical research.

In the words of a chemist, "Triphenylmethanol is not just a compound; it’s a gateway to understanding complex organic processes and reactions." This underscores its importance in both academic research and real-world applications.

Overall, triphenylmethanol serves as a prime example of how a simple molecule can have profound implications across various fields of chemical science.

Synonyms
TRIPHENYLMETHANOL
76-84-6
Triphenylcarbinol
Trityl alcohol
Tritanol
Triphenyl methanol
Triphenylmethyl alcohol
Methanol, triphenyl-
Triphenyl-methanol
Benzenemethanol, .alpha.,.alpha.-diphenyl-
hydroxytriphenylmethane
Fimasartan Impurity L
MFCD00004445
tritylalcohol
triphenyl carbinol
NSC 4050
U97Q0OU9KB
Zidovudine impurity D
NSC-4050
EINECS 200-988-5
Benzenemethanol, alpha,alpha-diphenyl-
TRIPHENYLCARBINOL [MI]
AI3-08929
CHEMBL118166
DTXSID0058803
TRIPHENYLMETHANOL [USP-RS]
ZIDOVUDINE IMPURITY D [WHO-IP]
ZIDOVUDINE IMPURITY D [EP IMPURITY]
LOSARTAN POTASSIUM IMPURITY G [EP IMPURITY]
TRIPHENYLMETHANOL (USP-RS)
ZIDOVUDINE IMPURITY D (EP IMPURITY)
LOSARTAN POTASSIUM IMPURITY G (EP IMPURITY)
UNII-U97Q0OU9KB
Methanol, triphenyl
Ph3COH
Triphenylmethanol, 97%
SCHEMBL700
Methanol, triphenyl (8CI)
Methanol, triphenyl-(8CI)
DTXCID9047835
alpha,alphaDiphenylbenzenemethanol
BDBM23784
LZTRCELOJRDYMQ-UHFFFAOYSA-
Triphenylcarbinol, Trityl alcohol
NSC4050
CHEBI:228440
Benzenemethanol, alpha,alphadiphenyl
MFCD10565638
STK370823
AKOS002265728
.alpha.,.alpha.-Diphenyl-benzylalcohol
CS-W012504
HY-W011788
IT28577
Triphenylmethyl-containing compound, 13
AS-11948
BP-12571
SY025338
DB-056145
NS00037849
T0516
Triphenylmethanol, purum, >=98.0% (HPLC)
H11234
EN300-1654565
AR-360/42760202
U-45483
Q2735403
F1908-0150
Z3018664754
Trityl alcohol resin (100-200 mesh, 2.1-4.0 mmol/g)
Triphenylmethanol, United States Pharmacopeia (USP) Reference Standard
Zidovudine impurity D, European Pharmacopoeia (EP) Reference Standard
a,a-Diphenylbenzenemethanol;Zidovudine Impurity D;Hydroxytriphenylmethane;BL 3756
InChI=1/C19H16O/c20-19(16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15,20H