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Indene - analytical standard，for environmental analysis，>99.0%(GC), high purity , CAS No.95-13-6

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Indene - analytical standard，for environmental analysis，>99.0%(GC), high purity , CAS No.95-13-6

5 Citations

COA

Grade & Purity:

analytical standard

for environmental analysis

≥99%(GC)

Cas Number: 95-13-6
Molecular Weight: 116.16
Beilstein Registry Number: 635873
EC Number: 202-393-6
MDL number: MFCD00003777
PubChem CID: 7219

In stock

Item Number

I105569

Grouped product items
SKU	Size	Availability	Price	Qty
I105569-250mg	250mg	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$137.90

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	analytical standard, for environmental analysis, ≥99%(GC)
Storage Temp	Argon charged
Shipped In	Normal
Grade	analytical standard, for environmental analysis

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Class Indenes and isoindenes

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
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Associated Targets(Human)

CES1 Tchem Acyl coenzyme A:cholesterol acyltransferase (1029 Activities)

Discover Target: CES1

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:

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1 results found

Lot Number	Certificate Type	Date	Item
K2108116	Certificate of Analysis	Aug 01, 2023	I105569

Chemical and Physical Properties

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 Å²
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

Alternative Products

Citations of This Product

How to Cite Aladdin Scientific Products?

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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