Skip to Content
Merck
All Photos(1)

Documents

526037

Sigma-Aldrich

Cyclopentanecarboxaldehyde

95%

Synonym(s):

Cyclopentanealdehyde, Cyclopentanecarbaldehyde, Cyclopentyl aldehyde, Cyclopentylformaldehyde, Formylcyclopentane

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
C5H9CHO
CAS Number:
Molecular Weight:
98.14
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

95%

contains

0.1% hydroquinone as stabilizer

refractive index

n20/D 1.4430 (lit.)

bp

140-141 °C (lit.)

density

0.919 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

[H]C(=O)C1CCCC1

InChI

1S/C6H10O/c7-5-6-3-1-2-4-6/h5-6H,1-4H2

InChI key

VELDYOPRLMJFIK-UHFFFAOYSA-N

General description

Cyclopentanecarboxaldehyde can be prepared from cyclohexene, via copper-catalyzed oxidation with persulfate. It can also be synthesized from mercuric sulfate and cyclohexene.

Application

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

Pictograms

FlameExclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Aquatic Chronic 3 - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

82.9 °F - closed cup

Flash Point(C)

28.3 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Mechanism of oxidation of the 2-hydroxycyclohexyl radical to cyclopentanecarbaldehyde by copper ions in aqueous solutions.
Masarwa M, et al.
Inorganic Chemistry, 30(8), 1849-1854 (1991)
Cyclopentanecarboxaldehyde.
Grummitt O, et al.
Organic Syntheses, 26-26 null
2-Hydroxycyclohexylhydrazines. II. 1 Reaction with Nitrous Acid.
Taguchi T, et al.
The Journal of Organic Chemistry, 29(5), 1104-1106 (1964)
The Synthesis of Some δ-Lactones of α,β,δ-Trihydroxy Acids1.
English Jr J, et al.
Journal of the American Chemical Society, 73(2), 615-618 (1951)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service