Skip to Content
Merck
All Photos(1)

Key Documents

W510505

Sigma-Aldrich

Undecane

≥99%

Synonym(s):

n-Undecane, Hendecane

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CH3(CH2)9CH3
CAS Number:
Molecular Weight:
156.31
Beilstein:
1697099
EC Number:
MDL number:
UNSPSC Code:
12164502
PubChem Substance ID:
NACRES:
NA.21

biological source

synthetic

Quality Level

grade

Fragrance grade

Agency

follows IFRA guidelines

reg. compliance

EU Regulation 1223/2009
FDA 21 CFR 117

vapor density

5.4 (vs air)

vapor pressure

<0.4 mmHg ( 20 °C)

Assay

≥99%

refractive index

n20/D 1.417 (lit.)

bp

196 °C (lit.)

mp

−26 °C (lit.)

density

0.74 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

Documentation

see Safety & Documentation for available documents

food allergen

no known allergens

fragrance allergen

no known allergens

Organoleptic

faint

SMILES string

CCCCCCCCCCC

InChI

1S/C11H24/c1-3-5-7-9-11-10-8-6-4-2/h3-11H2,1-2H3

InChI key

RSJKGSCJYJTIGS-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

Undecane is a saturated hydrocarbon that is reported to occur in the volatile oil extracted from powder and leaf of Hypericum triquetrifolium Turra, leaves of Solanum aculeastrum and flowers of Pittosporum tobira.

Application


  • Preparation and Performance Study of n-Undecane Phase Change Cold Storage Material.: This study focuses on the preparation and performance of n-undecane as a phase change material for cold storage applications. The research highlights its thermal properties and potential use in energy storage systems, offering advancements in material science and energy efficiency (Yan et al., 2024).

Disclaimer

For R&D or non-EU Food use. Not for retail sale.

Pictograms

FlameHealth hazard

Signal Word

Danger

Hazard Statements

Hazard Classifications

Asp. Tox. 1 - Flam. Liq. 3

Supplementary Hazards

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

140.0 °F - closed cup

Flash Point(C)

60 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

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

Visit the Document Library

Isolation of volatile compounds from Solanum aculeastrum (Solanaceae).
Koduru S, et al.
Journal of Essential Oil-Bearing Plants, 9(1), 65-69 (2006)
Volatile constituents of Pittosporum tobira (Thunb.) Aiton fil cultivated in Greece.
Loukis A & Hatziioannou C.
J. Essent. Oil Res., 17(2), 186-187 (2005)
Volatile constituents of the leaves and flowers of Hypericum triquetrifolium Turra.
Bertoli A, et al.
Flavour and Fragrance Journal, 18(2), 91-94 (2003)
Maya M Makatini et al.
Bioorganic & medicinal chemistry letters, 21(8), 2274-2277 (2011-03-25)
In this study, we present the first account of pentacycloundecane (PCU) peptide based HIV-protease inhibitors. The inhibitor exhibiting the highest activity made use of a natural HIV-protease substrate peptide sequence, that is, attached to the cage (PCU-EAIS). This compound showed
Igor Shamovsky et al.
Journal of medicinal chemistry, 52(23), 7706-7723 (2009-12-04)
The metabolic stability and selectivity of a series of CCR8 antagonists against binding to the hERG ion channel and cytochrome Cyp2D6 are studied by principal component analysis. It is demonstrated that an efficient way of increasing metabolic stability and selectivity

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