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Triphenylmethanol

Product Name
Triphenylmethanol
CAS No.
76-84-6
Chemical Name
Triphenylmethanol
Synonyms
TRT-OH;TRIPHENYLCARBINOL;TRITYL ALCOHOL;Tritanol;Triphenylmethanol, (Triphenyl carbinol;Ih-Tetrazole;tirphenylmethanol;Triphenylmethanol ,99%;Triphenylmethyl alcohol;Triphenylmethanol(76-84-6)
CBNumber
CB3335936
Molecular Formula
C19H16O
Formula Weight
260.33
MOL File
76-84-6.mol
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Triphenylmethanol Property

Melting point:
160-163 °C (lit.)
Boiling point:
360 °C (lit.)
Density 
d40 1.199
refractive index 
1.6220 (estimate)
Flash point:
360-380°C
storage temp. 
2-8°C
solubility 
dioxane: 0.1 g/mL, clear
pka
12.73±0.29(Predicted)
form 
Fine Crystalline Powder
color 
White to light yellow
Appearance
White to Light yellow to Light orange powder to crystal
Water Solubility 
INSOLUBLE
Merck 
14,9739
BRN 
1460837
Stability:
Stable. Combustible. Incompatible with oxidizing agents, acids, acid chlorides, acid anhydrides.
CAS DataBase Reference
76-84-6(CAS DataBase Reference)
NIST Chemistry Reference
Benzenemethanol, «alpha»,«alpha»-diphenyl-(76-84-6)
EPA Substance Registry System
Benzenemethanol, .alpha.,.alpha.-diphenyl- (76-84-6)
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Safety

Hazard Codes 
Xi
Risk Statements 
38-36/37/38
Safety Statements 
22-24/25-36-26
WGK Germany 
3
TSCA 
Yes
HS Code 
29062900
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P405Store locked up.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
Y0001654
Product name
Zidovudine impurity D
Purity
European Pharmacopoeia (EP) Reference Standard
Packaging
15 mg
Price
$118
Updated
2025/07/31
Sigma-Aldrich
Product number
PHR3668
Product name
Losartan Impurity G
Purity
certified reference material, pharmaceutical secondary standard
Packaging
1 unit
Price
$524
Updated
2025/07/31
Sigma-Aldrich
Product number
8.21196
Product name
Triphenylmethanol
Purity
for synthesis
Packaging
50g
Price
$77.7
Updated
2025/07/31
Sigma-Aldrich
Product number
8.21196
Product name
Triphenylmethanol
Purity
for synthesis
Packaging
250g
Price
$206
Updated
2025/07/31
Sigma-Aldrich
Product number
134848
Product name
Triphenylmethanol
Purity
97%
Packaging
50g
Price
$71
Updated
2025/07/31
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Triphenylmethanol Chemical Properties,Usage,Production

Chemical Properties

Triphenylmethanol is a white powder or colorless, isolated crystals that are soluble in alcohol, ether, and benzene. It turns dark yellow when dissolved in concentrated sulfuric acid, colorless when dissolved in glacial acetic acid, and is insoluble in water and petroleum ether. It distills at 360-380°C without decomposition.

Uses

Triphenylmethanol is used as a reagent in the research laboratory. It acts as an intermediate in the production of the commercially useful triarylmethane dyes. It is used in the preparation of triphenylmethane. It is also used as an antiproliferative agent. Further, it is used in the preparation of two-electron reduction product of pyrylogen. In addition to this, it reacts with triphenylphosphine oxide to form a 1:1 molecular complex. It serves as a specific clathrate host for methanol and dimethyl sulphoxide and forms clathrate inclusion complexes.
Triphenylmethanol was used in the synthesis of of the two-electron reduction product of pyrylogen.
It undergoes reduction to triphenylmethane by 9, 10-dihydro-10-methylacridine in the presence of perchloric acid.

Uses

Triphenylmethanol (Zidovudine EP Impurity D) is a triaryl methane derivative as antiproliferative agent.

Preparation

Triphenylmethanol synthesis: Triphenylmethanol was prepared by the action of benzene with carbon tetrachloride in the presence of Aluminum chloride, followed by acidification and hydrolysis.
Triphenylmethanol can also be prepared by the reaction of phenylmagnesium bromide with methyl benzoate (instead of benzophenone).
Synthesis of Triphenylmethanol

Reactions

The first one is the formation of the triphenylmethyl bromide from the reaction of triphenylmethanol with hydrobromic acid.
The second reaction is the formation of an ether from the reaction of triphenylmethanol with methanol in acidic conditions.

Synthesis Reference(s)

Organic Syntheses, Coll. Vol. 3, p. 839, 1955
The Journal of Organic Chemistry, 57, p. 4555, 1992 DOI: 10.1021/jo00042a044

General Description

Triphenylmethanol forms 1:1 molecular complex with triphenylphosphine oxide. It is a specific clathrate host for methanol and dimethyl sulphoxide and forms clathrate inclusion complexes. It undergoes reduction to triphenylmethane by 9, l0-dihydro-10-methylacridine in the presence of perchloric acid.

Materials Uses

Triphenylmethanol (TPOH) is a non-fluorescent compound that emits strong fluorescence in an aggregate state or on a solid surface after irradiation by UV light at 254 nm (UV1). Interestingly, the photo-induced fluorescence of TPOH was quenched when irradiated by UV light at a longer wavelength of 365 nm (UV2) and further repeatable on and off by UV1 and UV2, respectively. The reversible activation and deactivation of fluorescence at a solid surface could be repeatable at least 5 times. TPOH is thus applied for rewritable photopatterning tuned by UV light[1].

Purification Methods

Crystallise the carbinol from EtOH, MeOH, CCl4 (4mL/g), *benzene, hexane or pet ether (b 60-70o). Dry it at 90o. [Ohwada et al. J Am Chem Soc 108 3029 1986, Beilstein 6 IV 5014.]

References

[1] Zheng, Yue et al. “Photoactivatable aggregation-induced emission of triphenylmethanol?.” Chemical Communications 81 (2017): 11130–11133.

Triphenylmethanol Preparation Products And Raw materials

Raw materials

Preparation Products

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Triphenylmethanol Suppliers

Suzhou Yuanrui Bio-Tech Co., Ltd
Tel
18106132862
Email
info@yuanruibio.com
Country
China
ProdList
299
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58
Dongyang Baihang Chemical Co., Ltd.
Tel
0579-86886233 18006543966
Fax
QQ:355093164
Email
355093164@qq.com
Country
China
ProdList
108
Advantage
58
Apeloa Pharmaceutical Co., Ltd.
Tel
+86-0571-87635730 +86-13588737631
Email
inquiry@hengdian-group.com
Country
China
ProdList
176
Advantage
58
Shandong Mingde Biotechnology Co., Ltd
Tel
15564477061
Email
1397986535@qq.com
Country
China
ProdList
298
Advantage
58
Shandong Scientific Research Pharmaceutical Co., Ltd
Tel
13053388939
Email
3908585847@qq.com
Country
China
ProdList
82
Advantage
58
Shandong Jialian New Materials Co., Ltd
Tel
18560999950; 18560999950
Email
905978557@qq.com
Country
China
ProdList
20
Advantage
58
Shandong Lierbang New Material Co. LTD
Tel
15553337722
Email
1135818881@qq.com
Country
China
ProdList
33
Advantage
58
J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006356688 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40228
Advantage
62
3B Pharmachem (Wuhan) International Co.,Ltd.
Tel
821-50328103-801 18930552037
Fax
86-21-50328109
Email
3bsc@sina.com
Country
China
ProdList
15838
Advantage
69
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View Lastest Price from Triphenylmethanol manufacturers

ZHENGZHOU JIUYI TIME NEW MATERIALS CO,.LTD
Product
Tritanol 76-84-6
Price
US $50.00-10.00/kg
Min. Order
1kg
Purity
99%,Electronic grade(Single metal impurity≤ 100ppb) or pharmaceutical grade
Supply Ability
100kg
Release date
2025-09-02
Hebei Chuanghai Biotechnology Co., Ltd
Product
Triphenylmethanol 76-84-6
Price
US $10.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
10 mt
Release date
2024-11-21
Hebei Zhuanglai Chemical Trading Co.,Ltd
Product
Triphenylmethanol 76-84-6
Price
US $70.00-25.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
20ton
Release date
2024-06-05

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