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HCID 6457생성일: 2026년 10월 27일

트리페닐메탄올

트라이페닐메틴올 · 트리페닐메탄올 · TRT-OH · TRIPHENYLCARBINOL · TRITYL ALCOHOL · Triphenylmethanol, (Triphenyl carbinol · Methanol, triphenyl- · Tritanol

https://huagongshe.com/ko/chemical/6457

트리페닐메탄올 분자 구조식

식별자 및 물리적 특성

CAS No.76-84-6
분자식C19H16O
평균 분자량260.3 g/mol
단동위원소 질량260.12011513 g/mol
SMILESOC(c1ccccc1)(c1ccccc1)c1ccccc1
InChIKeyLZTRCELOJRDYMQ-UHFFFAOYSA-N
PubChem CID6457
ChEMBLCHEMBL118166
ChEBICHEBI:228440
EC No.200-988-5
DTXSIDDTXSID0058803
현지명트리페닐메탄올

화학 및 물리적 성질

XLogP3.7
극성 표면적20.2
수소 결합 공여자 수1
수소 결합 수용자 수1
회전 가능 결합 수3
무거운 원자 수20
형식 전하0
복잡도235
PolymersOther Classes -> Alcohols and Polyols, Other
SpringerMaterials Properties13C nuclear magnetic resonance spectrum
LogP(분배 계수)3.68
증기압0.00000003 [mmHg]
Physical DescriptionOther Solid[Merck Index] White to cream crystalline powder[Alfa Aesar MSDS]
녹는점160-163 °C (lit.)
끓는 점360 °C (lit.)
밀도d40 1.199
굴절률1.6220 (estimate)
인화점360-380°C
저장 조건2-8°C
용해도디옥산: 0.1 g/mL, 투명
pKa(산도 계수)12.73±0.29(Predicted)
물리적 상태미세 결정성 분말
색상흰색에서 밝은 노란색
용해도불용성
Merck14,9739
BRN1460837
안정성안정적인. 타기 쉬운. 산화제, 산, 산 염화물, 산 무수물과 호환되지 않습니다.
InChI1S/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
InChIKeyLZTRCELOJRDYMQ-UHFFFAOYSA-N
SMILESOC(c1ccccc1)(c2ccccc2)c3ccccc3
NISTBenzenemethanol, «alpha»,«alpha»-diphenyl-(76-84-6)
EPABenzenemethanol, .alpha.,.alpha.-diphenyl- (76-84-6)

화학적 성질

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.

안전 및 규제

GHS 분류This chemical does not meet GHS hazard criteria for 0.9% (1 of 114) of reports.WarningH315 (98.2%): Causes skin irritation [Warning Skin corrosion/irritation]P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 114 reports by companies from 9 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
규제 정보Chemical: Benzenemethanol, .alpha.,.alpha.-diphenyl-Benzenemethanol, .alpha.,.alpha.-diphenyl- is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Benzenemethanol, .alpha.,.alpha.-diphenyl- are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)Status: Active Update: 14-03-2019 https://echa.europa.eu/registration-dossier/-/registered-dossier/21505Benzenemethanol, .alpha.,.alpha.-diphenyl-: Does not have an individual approval but may be used under an appropriate group standard
유해성 요약A skin and strong eye irritant[Alfa Aesar MSDS] See Chlorotriphenylmethane and Triphenylmethyl bromide.
Hazard Classes and CategoriesSkin Irrit. 2 (98.2%)
수질 위해 등급(WGK)3
TSCA 등재 상태TSCA listed
관세 코드29062900
위험 문구(R)38-36/37/38
위험 표시Xi
안전 문구(S)22-24/25-36-26
기존화학 물질2001-3-1908
저장 분류11 - Combustible Solids

용도

용도

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.

일반 설명

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.

제조 및 합성 방법

제조 방법

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