Skip to Content
Merck
All Photos(3)

Key Documents

View All Documentation

258563

Sigma-Aldrich

2-Methylpentanal

98%

Synonym(s):

2-Methylvaleraldehyde

Sign Into View Organizational & Contract Pricing
All Photos(3)

About This Item

Linear Formula:
CH3CH2CH2CH(CH3)CHO
CAS Number:
123-15-9
Molecular Weight:
100.16
Beilstein:
1739423
EC Number:
204-605-2
MDL number:
MFCD00006986
UNSPSC Code:
12352100
PubChem Substance ID:
24855648
NACRES:
NA.22
Pricing and availability is not currently available.

vapor density

3.45 (vs air)

Quality Level

100

Assay

98%

form

liquid

autoignition temp.

390 °F

refractive index

n20/D 1.401 (lit.)

bp

119-120 °C (lit.)

density

0.808 g/mL at 25 °C (lit.)

functional group

aldehyde

SMILES string

CCCC(C)C=O

InChI

1S/C6H12O/c1-3-4-6(2)5-7/h5-6H,3-4H2,1-2H3

InChI key

FTZILAQGHINQQR-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

Cross-aldol condensation reaction of 2-methylpentanal with propanal to form 2,4-dimethylhept-2-enal has been investigated[1]. Oxidation of 2-methylpentanal with azidotrimetlzylsilane and chromic anhydride in CH2Cl2 has been investigated[2].

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Danger

Hazard Statements

H225,H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

60.8 °F - closed cup

Flash Point(C)

16 °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
MKCV0387
MKCT9503
MKCT6689
MKCN1937
MKCG7248

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.

Search for a COA

Already Own This Product?

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

Visit the Document Library

Oxidation of aldehydes to acyl azides by chromic anhydride-azidotrimethylsilane.
Lee JG and Kwak KH.
Tetrahedron Letters, 33(22), 3165-3166 (1992)
Valentina Innamorato et al.
Food chemistry, 315, 126247-126247 (2020-02-02)
Three non-targeted methods, i.e. 1H NMR, LC-HRMS, and HS-SPME/MS-eNose, combined with chemometrics, were used to classify two table grape cultivars (Italia and Victoria) based on five quality levels (5, 4, 3, 2, 1). Grapes at marketable quality levels (5, 4
Sajjad Ahmad et al.
Drug design, development and therapy, 15, 1299-1313 (2021-04-02)
Organocatalytic asymmetric Michael addition is a strong approach for C-C bond formation. The objective of the study is to design molecules by exploiting the efficiency of Michael Adducts. We proceeded with the synthesis of Michael adducts by tailoring the substitution
Christian P Mehnert et al.
Chemical communications (Cambridge, England), (15), 1610-1611 (2002-08-13)
C9-aldehyde has been prepared via aldol condensation reactions in ionic liquid media; catalyst investigation showed enhanced product selectivity for the desired aldehyde in ionic liquid media than in conventional solvent systems.

Questions

Reviews

No rating value

Active Filters

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