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Indene - 98%, high purity , CAS No.95-13-6

    Grade & Purity:
  • ≥98%
In stock
Item Number
I105568
Grouped product items
SKU Size
Availability
Price Qty
I105568-5ml
5ml
1
$30.90
I105568-25ml
25ml
1
$116.90
I105568-50ml
50ml
1
$210.90
I105568-100ml
100ml
1
$378.90

Basic Description

Synonyms HSDB 5286 | indene, (1H-indene) | Q27115417 | A845191 | INDENE | Q421008 | CAS-95-13-6 | CHEBI:41921 | Inden | F0001-2266 | 1H-Indene | EN300-19944 | STL268869 | DTXCID6022052 | Indenyl radical | D72500 | I0354 | Indonaphthene | BS-22312 | WLN: L56 BHJ |
Specifications & Purity ≥98%
Storage Temp Store at 2-8°C,Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class Indenes and isoindenes
Subclass Not available
Intermediate Tree Nodes Not available
Direct Parent Indenes and isoindenes
Alternative Parents Aromatic hydrocarbons  Polycyclic hydrocarbons  Cyclic olefins  
Molecular Framework Aromatic homopolycyclic compounds
Substituents Indene - Aromatic hydrocarbon - Polycyclic hydrocarbon - Cyclic olefin - Unsaturated hydrocarbon - Olefin - Hydrocarbon - Aromatic homopolycyclic compound
Description This compound belongs to the class of organic compounds known as indenes and isoindenes. These are compounds containing an indene moiety(which consists of a cyclopentadiene fused to a benzene ring), or a isoindene moiety (which consists of a cyclopentadiene fused to cyclohexadiene ring).
External Descriptors ortho-fused bicyclic arene - indene

Associated Targets(Human)

CES1 Tchem Acyl coenzyme A:cholesterol acyltransferase (1029 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

IUPAC Name 1H-indene
INCHI InChI=1S/C9H8/c1-2-5-9-7-3-6-8(9)4-1/h1-6H,7H2
InChIKey YBYIRNPNPLQARY-UHFFFAOYSA-N
Smiles C1C=CC2=CC=CC=C21
Isomeric SMILES C1C=CC2=CC=CC=C21
WGK Germany 1
RTECS NK8225000
UN Number 1993
Packing Group I
Molecular Weight 116.16
Beilstein 635873
Reaxy-Rn 635873
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=635873&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

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.

15 results found

Lot Number Certificate Type Date Item
H2405342 Certificate of Analysis Jul 26, 2024 I105568
H2405558 Certificate of Analysis Jul 26, 2024 I105568
B2507088 Certificate of Analysis Jul 26, 2024 I105568
F2414059 Certificate of Analysis Apr 07, 2024 I105568
D2416338 Certificate of Analysis Apr 07, 2024 I105568
D2416339 Certificate of Analysis Apr 07, 2024 I105568
D2416340 Certificate of Analysis Apr 07, 2024 I105568
D2416341 Certificate of Analysis Apr 07, 2024 I105568
D2416342 Certificate of Analysis Apr 07, 2024 I105568
K2201445 Certificate of Analysis Oct 21, 2022 I105568
K2201447 Certificate of Analysis Oct 21, 2022 I105568
K2201446 Certificate of Analysis Oct 21, 2022 I105568
D2419067 Certificate of Analysis Oct 21, 2022 I105568
H1807099 Certificate of Analysis Jun 15, 2022 I105568
H1807100 Certificate of Analysis Jun 15, 2022 I105568

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Chemical and Physical Properties

Solubility Insoluble in water; Miscible with Ether,Alcohol
Sensitivity Air & Light sensitive.
Refractive Index 1.595
Flash Point(°F) 136.40℉
Flash Point(°C) 58°C
Boil Point(°C) 181-182°C
Melt Point(°C) -5--3°C
Molecular Weight 116.160 g/mol
XLogP3 2.900
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 0
Rotatable Bond Count 0
Exact Mass 116.063 Da
Monoisotopic Mass 116.063 Da
Topological Polar Surface Area 0.000 Ų
Heavy Atom Count 9
Formal Charge 0
Complexity 124.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Citations of This Product

1. Tian Zhao, Hexin Zhu, Ming Dong.  (2020)  Comparison of Catalytic Activity of Chromium–Benzenedicarboxylate Metal–Organic Framework Based on Various Synthetic Approach.  Catalysts,  10  (3): (318). 
2. Yimeng Wang, Jie Wang.  (2016)  Multifaceted effects of HZSM-5 (Proton-exchanged Zeolite Socony Mobil-5) on catalytic cracking of pinewood pyrolysis vapor in a two-stage fixed bed reactor.  BIORESOURCE TECHNOLOGY,  214  (700). 
3. Zhongyue Zhou, Mingfeng Xie, Zhandong Wang, Fei Qi.  (2009)  Determination of absolute photoionization cross-sections of aromatics and aromatic derivatives.  RAPID COMMUNICATIONS IN MASS SPECTROMETRY,  23  (24): (3994-4002). 
4. Yuwen Deng, Zaili Xiong, Jijun Guo, Chen Huang, Long Zhao, Meirong Zeng, Zhongyue Zhou, Wenhao Yuan, Fei Qi.  (2025)  An experimental and modeling study on indene oxidation: Emphasizing the competing kinetics between PAH oxidative decomposition and mass growth.  COMBUSTION AND FLAME,  272  (113912). 
5. Yuwen Deng, Zaili Xiong, Jijun Guo, Bingzhi Liu, Meirong Zeng, Zhandong Wang, Zhongyue Zhou, Wenhao Yuan, Fei Qi.  (2024)  Ozone-assisted low temperature oxidation of indene: An experimental and computational study.  PROCEEDINGS OF THE COMBUSTION INSTITUTE,  40  (105371). 

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