Diphenylmethane - ≥99% , CAS No.101-81-5

CAS: 101-81-5 Cat. No.: D105756 Peso molecular: 168.23 Beilstein Registry Number: 1904982 Número EC: 202-978-6
Disponible para pedir
GRADE & PURITY ≥99%
Synonyms
DTXCID9021891 | AI3-28021-X | EINECS 202-978-6 | EN300-21054 | Benzylbenzene | benzyl-benzene | Diphenylmethane, 99% | E75810 | Toluene, .alpha.-phenyl- | Diphenylmethan | Toluene, alpha-phenyl- | DTXSID1041891 | Tox21_301147 | alpha-phenyltoluene | Ditan
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
25g
D105756-25g
3

13,90US$

20,90US$
Guardar 7,00 US$ (33.49%)
50g
D105756-50g
4

15,90US$

23,90US$
Guardar 8,00 US$ (33.47%)
100g
D105756-100g
4

16,90US$

25,90US$
Guardar 9,00 US$ (34.75%)
250g
D105756-250g
3

22,90US$

34,90US$
Guardar 12,00 US$ (34.38%)
500g
D105756-500g
2

28,90US$

43,90US$
Guardar 15,00 US$ (34.17%)
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Why this grade

≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 20 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Diphenylmethane is an aromatic compound used as a key building block in the synthesis of elastase inhibitors.
Application
Diphenylmethane is widely used in the synthesis of luminogens for aggregation-induced emission (AIE).
It is used in the preparation of a polymerization initiator, diphenylmethyl potassium (DPMK).
It is one of the precursors in the synthesis of a dendrimeric polycyclic aromatic hydrocarbon (PAH), hexakis[4-(1,1,2-triphenyl-ethenyl)phenyl]benzene.

Specifications

Sinónimos
DTXCID9021891 | AI3-28021-X | EINECS 202-978-6 | EN300-21054 | Benzylbenzene | benzyl-benzene | Diphenylmethane, 99% | E75810 | Toluene, .alpha.-phenyl- | Diphenylmethan | Toluene, alpha-phenyl- | DTXSID1041891 | Tox21_301147 | alpha-phenyltoluene | Ditan
Especificaciones y pureza
≥99%
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Pureza
≥99%
Nombres e identificadores
Pubchem Sid504751399
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504751399
Sonrisas canónicasC1=CC=C(C=C1)CC2=CC=CC=C2
IUPAC Namebenzylbenzene
InChIKeyCZZYITDELCSZES-UHFFFAOYSA-N
INCHI1S/C13H12/c1-3-7-12(8-4-1)11-13-9-5-2-6-10-13/h1-10H,11H2
Isómeros SMILES C1=CC=C(C=C1)CC2=CC=CC=C2
WGK Alemania 2
RTECS DA4976500
Peso molecular 168.23
Beilstein 1904982
Reaxy-Rn 1904982
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1904982&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClaseBenzene and substituted derivatives
SubclassDiphenylmethanes
Intermediate Tree Nodes Not available
Direct ParentDiphenylmethanes
Alternative Parents Aromatic hydrocarbons  Unsaturated hydrocarbons  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Diphenylmethane - Aromatic hydrocarbon - Unsaturated hydrocarbon - Hydrocarbon - Aromatic homomonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as diphenylmethanes. These are compounds containing a diphenylmethane moiety, which consists of a methane wherein two hydrogen atoms are replaced by two phenyl groups.
External Descriptors diarylmethane
Estructura 3D
Modelo de Estructura Química Interactiva





Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

26 results found

Lot NumberCertificate TypeFechaArticulo
F2605091Certificate of AnalysisJun 15, 2026 D105756
I2215590Certificate of AnalysisJun 15, 2026 D105756
I2215589Certificate of AnalysisJun 15, 2026 D105756
L2512028Certificate of AnalysisDec 23, 2025 D105756
G2508387Certificate of AnalysisJun 30, 2025 D105756
G2508386Certificate of AnalysisJun 30, 2025 D105756
G2508351Certificate of AnalysisJun 30, 2025 D105756
G2508374Certificate of AnalysisJun 30, 2025 D105756
H2125101Certificate of AnalysisJun 09, 2025 D105756
H2125100Certificate of AnalysisJun 09, 2025 D105756
E2523061Certificate of AnalysisMay 30, 2025 D105756
I2002154Certificate of AnalysisJun 06, 2024 D105756
I2002153Certificate of AnalysisJun 06, 2024 D105756
I2002152Certificate of AnalysisJun 06, 2024 D105756
F2016040Certificate of AnalysisApr 03, 2024 D105756
E2407370Certificate of AnalysisMar 23, 2024 D105756
B2519081Certificate of AnalysisAug 11, 2022 D105756
I2215576Certificate of AnalysisAug 11, 2022 D105756
I2215588Certificate of AnalysisAug 11, 2022 D105756
D2526064Certificate of AnalysisAug 11, 2022 D105756
D2408074Certificate of AnalysisAug 11, 2022 D105756
I2215591Certificate of AnalysisAug 11, 2022 D105756
I2215592Certificate of AnalysisAug 11, 2022 D105756
J2316020Certificate of AnalysisAug 11, 2022 D105756
J2418164Certificate of AnalysisAug 11, 2022 D105756
D2313831Certificate of AnalysisAug 11, 2022 D105756

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Propiedades químicas y físicas
SolubilidadSoluble in ethanol, ether, chloroform, etc.
Punto de congelación (°C)25 °C
Índice de refracción1.5753
Punto de inflamación (°F)260.6℉
Punto de inflamación (°C)127℃
Punto de ebullición (°C)264.3°C
Punto de fusión (°C)22-24°C
Peso molecular168.230 g/mol
XLogP34.100
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count0
Rotatable Bond Count2
Exact Mass168.094 Da
Monoisotopic Mass168.094 Da
Topological Polar Surface Area0.000 Ų
Heavy Atom Count13
Formal Charge0
Complexity111.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Referencias
1. Qifeng Yang, Yiming Mo.  (2023)  Direct Electrochemical Oxidation of Benzylic C–H Bond by La2O3@C/CP Composite Electrode with Water as the Green Oxygen Source.  INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH,      [PMID:] [10.1021/acs.iecr.3c02229]
2. Haobo Xie, Mingu Zhou, Xiaorui Cui, Chao Li, Yongjun Wu, Xinjuan Luo, Mao-Sen Yuan.  (2023)  A metal-complex based chemosensor for the detection of riboflavin and folate.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,      [PMID:37678046] [10.1016/j.saa.2023.123321]
3. Yang Feng, Min Sun, Mingxia Sun, Jiaqing Feng, Haili Sun, Juanjuan Feng.  (2022)  Extraction performance-structure relationship of polyamidoamine dendrimers on silica for online solid-phase extraction of organic pollutants.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:35576765] [10.1016/j.chroma.2022.463132]
4. Chong Wang, Yuchen Hou, Jiajia Cheng, Mei-Jin Lin, Xinchen Wang.  (2021)  Biomimetic donor-acceptor motifs in carbon nitrides: Enhancing red-light photocatalytic selective oxidation by rational surface engineering.  APPLIED CATALYSIS B-ENVIRONMENTAL,      [PMID:] [10.1016/j.apcatb.2021.120259]
5. Liyun Huang, Kui Wu, Qian He, Chao Xiong, Tao Gan, Xiaohui He, Hongbing Ji.  (2021)  Quasi-continuous synthesis of iron single atom catalysts via a microcapsule pyrolysis strategy.  AICHE JOURNAL,  67  (6): (e17197).  [PMID:] [10.1002/aic.17197]
6. Xingfei Tang, Wentao Ding, Hao Li.  (2020)  Improved hydrodeoxygenation of bio-oil model compounds with polymethylhydrosiloxane by Brønsted acidic zeolites.  FUEL,      [PMID:] [10.1016/j.fuel.2020.119883]
7. Shanshan Jie, Congqiang Yang, Yuan Chen, Zhigang Liu.  (2018)  Facile synthesis of ultra-stable Co-N-C catalysts using cobalt porphyrin and peptides as precursors for selective oxidation of ethylbenzene.  Molecular Catalysis,      [PMID:] [10.1016/j.mcat.2018.08.007]
8. Yuan Chen, Shanshan Jie, Congqiang Yang, Zhigang Liu.  (2017)  Active and efficient Co-N/C catalysts derived from cobalt porphyrin for selective oxidation of alkylaromatics.  APPLIED SURFACE SCIENCE,      [PMID:] [10.1016/j.apsusc.2017.04.246]
9. Zhong-Qiu Liu, Xian-Yong Wei, Xiao Zhou, Yu-Chuan Xiao, Zhan-Ku Li, Xian-Hou Guo, Sheng-Kang Wang, Yang-Yang Zhang, Zhi-Min Zong, Feng-Yun Ma, Jing-Mei Liu.  (2017)  An acidic ionic liquid modified microfiber attapulgite-supported nickel for catalytic hydroconversion of α,ω-diarylalkanes.  FUEL PROCESSING TECHNOLOGY,      [PMID:] [10.1016/j.fuproc.2017.03.011]
10. Miao Luo, Sheng Wang, Meiling Wang, Shaorong Huang, Chengpeng Li, Lin Chen, Xiang Ma.  (2016)  Novel organogel harnessing Excited-State Intramolecular Proton Transfer process with aggregation induced emission and photochromism.  DYES AND PIGMENTS,      [PMID:] [10.1016/j.dyepig.2016.04.036]
11. MIAO LUO, XIE ZHOU, ZHENGUO CHI, CHUNPING MA, YI ZHANG, SIWEI LIU, JIARUI XU.  (2013)  SYNTHESIS AND PROPERTIES OF GELATORS DERIVED FROM TETRAPHENYLETHYLENE AND GALLIC ACID WITH AGGREGATION-INDUCED EMISSION.  Journal of Molecular and Engineering Materials,      [PMID:] [10.1142/S2251237313400078]
12. Xuan Yan, Yucheng Liu, Zhengmeng Hou, Lina Yuan, Jun Yang, Wenxin Dong.  (2024)  Cleaning Oil-Based Drilling Cuttings with Synthetic Gemini Surfactants.  ACS Omega,      [PMID:38463275] [10.1021/acsomega.3c08618]
13. Min Sun, Jiaqing Feng, Yang Feng, Xubo Xin, Yali Ding, Juanjuan Feng.  (2024)  Core-shell silica@pyridyl conjugated microporous polymer as a stationary phase for high performance liquid chromatography.  ANALYTICA CHIMICA ACTA,      [PMID:38309855] [10.1016/j.aca.2024.342258]
14. Wenhua Hou, Lishuai Zong, Linyan Zhu, Jiaming Wang, Yabin Zhang, Zhansheng Li, Jinyan Wang, Xigao Jian.  (2024)  Design and synthesis of low-dieclectric polyaryl ethers containing bulky tetraphenyl vinyl pendant group.  POLYMERS FOR ADVANCED TECHNOLOGIES,  35  (4): (e6357).  [PMID:] [10.1002/pat.6357]
15. Meifang Cao, Yuqiao Ma, Tao Ruan, Lifeng Li, Bo Chen, Xueqing Qiu, Di Fan, Xinping Ouyang.  (2024)  Highly efficient hydrogenolysis of lignin into monophenol over an atomically dispersed platinum catalyst.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2024.150020]
16. Xiaomin Li, Mingxia Sun, Yang Feng, Yanming Liu, Yanli Wang, Juanjuan Feng, Min Sun.  (2024)  Ionic liquid-functionalized covalent organic frameworks on the surface of silica for online solid-phase extraction.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:39096780] [10.1016/j.chroma.2024.465200]
17. Weichuan Xu, Hong Huang, Lingling Bi, Haimei Xu, Zhichao Miao, Mei Wu.  (2024)  One-pot fabrication of vanadium-doped ordered mesoporous zirconium oxophosphate catalyst for the synthesis of carbonyl compounds.  NEW JOURNAL OF CHEMISTRY,  48  (24): (10820-10829).  [PMID:] [10.1039/D4NJ01661K]
18. Jingrong Li, Ying Wang, Tingting Xiao, Xinluona Su, Haiyang Cheng, Fengyu Zhao.  (2025)  Designing a Ru/TiO2 Catalyst with Ru Flat Island for Hydrogenation of Aromatic Compounds.  ACS Catalysis,      [PMID:] [10.1021/acscatal.5c03245]
19. Guo-Shan Zhu, Ren-Jie Hui, Jun Hu.  (2025)  Microdroplet Stabilization Enabled Direct Mass Spectrometric Identification of Electrogenerated Transient Carbocation Intermediates.  Advanced Science,      [PMID:41355586] [10.1002/advs.202518157]
20. Zong-Pin Fu, Yun-Peng Zhao, Yu-Fa Wu, Qi-Jie Zhou, Shu-Ting Hu, Le-Le Qiu, Fang-Jing Liu, Mei Zhong, Jing Liang, Jing-Pei Cao.  (2026)  Interfacial oxygen vacancies and Cu-Ni bimetallic sites synergistically enhance the catalytic hydroconversion of soluble portion from lignite thermal dissolution.  JOURNAL OF ANALYTICAL AND APPLIED PYROLYSIS,      [PMID:] [10.1016/j.jaap.2026.107623]
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