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Crystal Violet Lactone

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Identification
Molecular formula
C27H31NO
CAS number
1552-42-7
IUPAC name
bis[4-(dimethylamino)phenyl]-phenyl-methanol
State
State

Crystal Violet Lactone is generally found as a solid at room temperature.

Melting point (Celsius)
184.00
Melting point (Kelvin)
457.15
Boiling point (Celsius)
443.00
Boiling point (Kelvin)
716.15
General information
Molecular weight
407.58g/mol
Molar mass
407.5750g/mol
Density
1.4200g/cm3
Appearence

Crystal Violet Lactone typically appears as a crystalline solid or powder. It is often colorless or white in its pure form.

Comment on solubility

Solubility of bis[4-(dimethylamino)phenyl]-phenyl-methanol

When examining the solubility of bis[4-(dimethylamino)phenyl]-phenyl-methanol, it is essential to consider both its molecular structure and the nature of its functional groups. This compound, with its extensive aromatic system and dimethylamino substituents, exhibits unique solubility characteristics.

Solubility Characteristics:

  • Polar Functional Groups: The presence of hydroxyl (–OH) and dimethylamino (–N(CH3)2) groups suggests potential for hydrogen bonding, enhancing solubility in polar solvents such as water.
  • Aromatic Rigidity: The aromatic rings may impart some hydrophobic properties, potentially limiting solubility in water but improving compatibility with organic solvents.
  • Solvent Specificity: Solubility is likely to be higher in organic polar solvents such as ethanol or methanol, while being lower in nonpolar solvents due to the compound's structure.

In summary, the solubility of bis[4-(dimethylamino)phenyl]-phenyl-methanol can be described as:

  1. Moderate in polar solvents
  2. Lower in nonpolar solvents

Overall, the interplay between its polar and nonpolar features makes this compound an intriguing subject for solubility studies, highlighting the importance of functional groups in physical chemistry.

Interesting facts

Exploring Bis[4-(dimethylamino)phenyl]-phenyl-methanol

Bis[4-(dimethylamino)phenyl]-phenyl-methanol, often abbreviated as BDMPM, is an intriguing organic compound primarily known for its applications in the field of organic electronics and dye-sensitized solar cells. Here are some captivating aspects of this compound:

  • Electron Donor: BDMPM functions as an excellent electron donor due to the presence of the dimethylamino groups, which enhance the charge transfer properties of the molecule.
  • Fluorescent Properties: This compound exhibits remarkable fluorescent characteristics, making it suitable for use in luminescent materials and sensors.
  • Structure and Stability: The sophisticated structure of BDMPM, featuring two para-dimethylamino phenyl groups, contributes to its overall stability and reactivity in various chemical environments.
  • Photonic Applications: With its unique photophysical properties, BDMPM is being investigated for applications in light-emitting devices, such as OLEDs (organic light-emitting diodes).

Further research into BDMPM and similar compounds could lead to significant advancements in materials science, particularly in creating more efficient and sustainable energy solutions. As quoted by the renowned chemist Linus Pauling, "The best way to have a good idea is to have lots of ideas." This encapsulates the ongoing exploration of BDMPM and its potential across various scientific fields.

Synonyms
Malachite Green Carbinol base
510-13-4
Malachite Green carbinol
Bis(p-(dimethylamino)phenyl)phenylmethanol
BRN 2222125
EINECS 208-109-7
UNII-680V7SFB75
680V7SFB75
Methanol, bis(p-(dimethylamino)phenyl)phenyl)-
Benzenemethanol, 4-(dimethylamino)-.alpha.-[4-(dimethylamino)phenyl]-.alpha.-phenyl-
DTXSID0060149
4-13-00-02278 (Beilstein Handbook Reference)
Benzenemethanol, 4-(dimethylamino)-alpha-(4-(dimethylamino)phenyl)-alpha-phenyl-
MALACHITE GREEN CARBINOL [MI]
MALACHITE GREEN (CARBINOL BASE)
BENZYL ALCOHOL, alpha,alpha-BIS(p-DIMETHYLAMINOPHENYL)-
4-(Dimethylamino)-alpha-(4-(dimethylamino)phenyl)-alpha-phenyl-benzenemethanol
BIS(P-DIMETHYLAMINOPHENYL)PHENYLMETHANOL
P,P'-(N,N-DIMETHYLAMINOTRIPHENYLMETHANOL
1,1-BIS(4-DIMETHYLAMINOPHENYL)-1-PHENYLMETHANOL
BIS(4-N,N-DIMETHYLAMINOPHENYL)PHENYLMETHYL ALCOHOL
Benzyl alcohol, .alpha.,.alpha.-bis(p-dimethylaminophenyl)-
4-(DIMETHYLAMINO)-.ALPHA.-(4-(DIMETHYLAMINO)PHENYL)-.ALPHA.-PHENYL BENZENEMETHANOL
4-(Dimethylamino)-.alpha.-(4-(dimethylamino)phenyl)-.alpha.-phenyl-benzenemethanol
BENZENEMETHANOL, 4-(DIMETHYLAMINO)-.ALPHA.-(4-(DIMETHYLAMINO)PHENYL)-.ALPHA.-PHENYL-
4-(Dimethylamino)-alpha-[4-(dimethylamino)phenyl]-alpha-phenyl-benzenemethanol
DTXCID1040952
Bis(p(dimethylamino)phenyl)phenylmethanol
Methanol, bis(p(dimethylamino)phenyl)phenyl)
alpha,alphaBis(pdimethylaminophenyl)benzyl alcohol
Benzyl alcohol, alpha,alphabis(pdimethylaminophenyl)
4(Dimethylamino)alpha(4(dimethylamino)phenyl)alphaphenylbenzenemethanol
Benzenemethanol, 4(dimethylamino)alpha(4(dimethylamino)phenyl)alphaphenyl
4(Dimethylamino)alpha(4(dimethylamino)phenyl)alphaphenylbenzenemethanol (9CI)
4-(DIMETHYLAMINO)-ALPHA-(4-(DIMETHYLAMINO)PHENYL)-ALPHA-PHENYL BENZENEMETHANOL
4-(Dimethylamino)-alpha-(4-(dimethylamino)phenyl)-alpha-phenyl-benzenemethanol (9CI)
208-109-7
lxhogendfzkpsf-uhfffaoysa-n
Solvent Green 1
bis[4-(dimethylamino)phenyl]-phenylmethanol
Carbinolbase des malachitgruen
MFCD00151208
C.I. Basic Green 4, carbinol
p,p'-bis(Dimethylamino)triphenylcarbinol
bis(4-(dimethylamino)phenyl)(phenyl)methanol
Methanol, bis[p-(dimethylamino)phenyl]phenyl-
METHANOL, BIS(P-(DIMETHYLAMINO)PHENYL)PHENYL-
Carbinolbase des malachitgruen [German]
alpha,alpha-Bis(p-dimethylaminophenyl)benzyl alcohol
bis[4-(dimethylamino)phenyl]phenylmethan-1-ol
SCHEMBL1450207
CHEBI:188911
HY-D1200
ICCB1_000128
ICCB1_000129
AKOS024282599
Malachite Green Carbinol base, 95.0%
SMP2_000062
triphenylcarbinol, 4,4'-bisdimethylamino-
CS-0143042
NS00000163
Bis[4-(dimethylamino)phenyl](phenyl)methanol #
Malachite Green Carbinol base, Dye content 90 %
Q27264186