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Cyclopentanecarboxaldehyde - 98%,contains 0.1% hydroquinone as stabilizer, high purity , CAS No.872-53-7

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Cyclopentanecarboxaldehyde - 98%,contains 0.1% hydroquinone as stabilizer, high purity , CAS No.872-53-7

1 Citations

COA

Grade & Purity:

≥98%
contains 0.1% hydroquinone as stabilizer

Cas Number: 872-53-7
Molecular Weight: 98.14
EC Number: 212-829-7
MDL number: MFCD00060798
PubChem CID: 70106

In stock

Item Number

C122650

Grouped product items
SKU	Size	Availability	Price
C122650-1g	1g	2	$30.90
C122650-5g	5g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$116.90
C122650-25g	25g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$399.90
C122650-100g	100g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$1,099.90

View related series

aldehyde (388) Non heterocyclic block (8163)

Basic Description

Synonyms	Cyclopentanecarbaldehyde, 0.1% hydroquinone as stabilizer \| cyclopentanecaboxaldehyde \| C3019 \| Formylcyclopentane \| Cyclopentanecarbaldehyde \| EN300-57255 \| Cyclopentanecarboxaldehyde (25ppm 1,4-Benzoquinone as stabiliser) \| BBL100156 \| Cyclopentanealdeh
Specifications & Purity	≥98%, contains 0.1% hydroquinone as stabilizer
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.
Product Description	Cyclopentanecarboxaldehyde can be prepared from cyclohexene, via copper-catalyzed oxidation with persulfate. It can also be synthesized from mercuric sulfate and cyclohexene. Cyclopentanecarboxaldehyde may be used in the synthesis of: · D,L-trans-2-cyclopentylmethylene-1-nitroso-1-(2-hydroxycyclohexyl)hydrazine · ethyl 5-cyclopentyl-5-hydroxy-2-pentenoate · ethyl 3-cyclo entyl-3-hydroxy-2-vinylpropanoate

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic oxygen compounds
  - Class Organic oxides

Kingdom	Organic compounds
Superclass	Organic oxygen compounds
Class	Organic oxides
Subclass	Not available
Intermediate Tree Nodes	Not available
Direct Parent	Organic oxides
Alternative Parents	Hydrocarbon derivatives Aldehydes
Molecular Framework	Aliphatic homomonocyclic compounds
Substituents	Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aldehyde - Aliphatic homomonocyclic compound
Description	This compound belongs to the class of organic compounds known as organic oxides. These are organic compounds containing an oxide group.
External Descriptors	Not available
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

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	cyclopentanecarbaldehyde
INCHI	InChI=1S/C6H10O/c7-5-6-3-1-2-4-6/h5-6H,1-4H2
InChIKey	VELDYOPRLMJFIK-UHFFFAOYSA-N
Smiles	C1CCC(C1)C=O
Isomeric SMILES	C1CCC(C1)C=O
WGK Germany	3
UN Number	1989
Molecular Weight	98.14
Reaxy-Rn	1560515
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1560515&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.

14 results found

Lot Number	Certificate Type	Date	Item
L2424606	Certificate of Analysis	Dec 16, 2024	C122650
L2424633	Certificate of Analysis	Dec 16, 2024	C122650
L2424609	Certificate of Analysis	Dec 16, 2024	C122650
L2424605	Certificate of Analysis	Dec 16, 2024	C122650
I2206463	Certificate of Analysis	Jun 13, 2024	C122650
I2206465	Certificate of Analysis	Jun 13, 2024	C122650
I2206462	Certificate of Analysis	Jun 13, 2024	C122650
J2126682	Certificate of Analysis	Aug 16, 2023	C122650
J2126689	Certificate of Analysis	Aug 16, 2023	C122650
J2126687	Certificate of Analysis	Aug 16, 2023	C122650
J2126685	Certificate of Analysis	Aug 16, 2023	C122650
E2113104	Certificate of Analysis	Feb 10, 2023	C122650
I2206464	Certificate of Analysis	Jun 22, 2022	C122650
E1814061	Certificate of Analysis	Feb 21, 2022	C122650

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Chemical and Physical Properties

Solubility	Soluble in water and ethanol
Sensitivity	Heat sensitive; Air sensitive
Refractive Index	1.443
Flash Point(°F)	82.4 °F
Flash Point(°C)	28 °C
Boil Point(°C)	140-141°C
Molecular Weight	98.140 g/mol
XLogP3	1.300
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	1
Rotatable Bond Count	1
Exact Mass	98.0732 Da
Monoisotopic Mass	98.0732 Da
Topological Polar Surface Area	17.100 Å²
Heavy Atom Count	7
Formal Charge	0
Complexity	62.600
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

How to Cite Aladdin Scientific Products?

1. Jing Zhang, Xun Kuang, Linyu Zhu, Xintong Xiao, Zhongyue Zhou, Fei Qi. (2025) Sustainable production of cyclohexanones through hydrodeoxygenation of lignin-derived phenolics over PdFe/HZSM-5 catalysts. FUEL, 383 (133863).

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