MedKoo Cat#: 464076 | Name: Triphenylcarbinol
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Description:

WARNING: This product is for research use only, not for human or veterinary use.

Triphenylmethanol (also known as triphenylcarbinol, TrOH) is an organic compound. It is a white crystalline solid that is insoluble in water and petroleum ether, but well soluble in ethanol, diethyl ether, and benzene. In strongly acidic solutions, it produces an intensely yellow color, due to the formation of a stable "trityl" carbocation. Many derivatives of triphenylmethanol are important dyes.

Chemical Structure

Triphenylcarbinol
Triphenylcarbinol
CAS#76-84-6

Theoretical Analysis

MedKoo Cat#: 464076

Name: Triphenylcarbinol

CAS#: 76-84-6

Chemical Formula: C19H16O

Exact Mass: 260.1201

Molecular Weight: 260.34

Elemental Analysis: C, 87.66; H, 6.20; O, 6.15

Price and Availability

Size Price Availability Quantity
50g USD 550.00 2 Weeks
250g USD 1,250.00 2 Weeks
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Related CAS #
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Synonym
Triphenylcarbinol; Triphenylmethanol; Triphenylmethyl alcohol; NSC 4050; NSC4050; NSC-4050; TrOH;
IUPAC/Chemical Name
triphenylmethanol
InChi Key
LZTRCELOJRDYMQ-UHFFFAOYSA-N
InChi Code
InChI=1S/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
SMILES Code
OC(c1ccccc1)(c2ccccc2)c3ccccc3
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO
Shelf Life
>2 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info
Solvent mg/mL mM
Solubility
Soluble in DMSO 0.0 100.00
Note: There can be variations in solubility for the same chemical from different vendors or different batches from the same vendor. The following factors can affect the solubility of the same chemical: solvent used for crystallization, residual solvent content, polymorphism, salt versus free form, degree of hydration, solvent temperature. Please use the solubility data as a reference only. Warming and sonication will facilitate dissolving. Still have questions? Please contact our Technical Support scientists.

Preparing Stock Solutions

The following data is based on the product molecular weight 260.34 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1: Mulkapuri S, Kurapati SK, Das SK. Carbonate encapsulation from dissolved atmospheric CO2 into a polyoxovanadate capsule. Dalton Trans. 2019 Jun 28;48(24):8773-8781. doi: 10.1039/c9dt01103j. Epub 2019 May 24. PMID: 31123747. 2: Vinatoru M, Bartha E, Badea F, Luche JL. Sonochemical and thermal redox reactions of triphenylmethane and triphenylmethyl carbinol in nitrobenzene. Ultrason Sonochem. 1998 Mar;5(1):27-31. doi: 10.1016/s1350-4177(98)00004-2. PMID: 11270332. 3: Tyrtysh TV, Baĭramova NE, Bovin NV. 1,6-angidro-N-atsetil-beta-D-gliukozamin v sinteze oligosakharidov. I. sinteze oligosakharidov. I. Sintez 3-atsetata i 3-benzoata 1,6-angidro-N=atsetil-beta-D-gliukozamina cherz 4-O-tritil'noe proizvodnoe [1,6-anhydro-N-acetyl-beta-D-glucosamines in synthesis of oligosaccharides. I. Synthesis of 3-acetate and 3-benzoate of 1,6-anhydro-N- acetyl-beta-D-glucosamine through a 4-O-trityl derivative]. Bioorg Khim. 2000 Jun;26(6):460-5. Russian. PMID: 10923195. 4: Cushman M, Kanamathareddy S, De Clercq E, Schols D, Goldman ME, Bowen JA. Synthesis and anti-HIV activities of low molecular weight aurintricarboxylic acid fragments and related compounds. J Med Chem. 1991 Jan;34(1):337-42. doi: 10.1021/jm00105a053. PMID: 1704066. 5: Newton DW, Breen PJ, Brown DE, Mackie JF Jr, Kluza RB. Physicochemical characteristics of patent blue violet dye. J Pharm Sci. 1981 Feb;70(2):122-7. doi: 10.1002/jps.2600700203. PMID: 7205212. 6: Griffiths MH. The metabolism of N-triphenylmethylmorpholine in the dog and rat. Biochem J. 1968 Aug;108(5):731-40. doi: 10.1042/bj1080731. PMID: 4876972; PMCID: PMC1198878. 7: Capellos C, Allen AO. Ionization of liquids by radiation: measurement by charge scavenging. Science. 1968 Apr 19;160(3825):302-3. doi: 10.1126/science.160.3825.302. PMID: 5641259. 8: Beynon KI, Wright AN. Break-down of the molluscicide N-tritylmorpholine in soil and in rice. Bull World Health Organ. 1967;37(1):65-72. PMID: 5300055; PMCID: PMC2554222. 9: Beynon KI, Thomas GR. Analytical methods for the determination of the molluscicide N-tritylmorpholine in water. Bull World Health Organ. 1967;37(1):47-52. PMID: 5300053; PMCID: PMC2554208. 10: CORNISH HH, ZAMORA E, BAHOR RE. METABOLISM OF TRIPHENYLMETHANE AND TRIPHENYLCARBINOL. Arch Biochem Biophys. 1964 Aug;107:319-24. doi: 10.1016/0003-9861(64)90337-6. PMID: 14224840.