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Key Documents

442719

Supelco

Nonanal

analytical standard

Synonym(s):

Aldehyde C9, Nonyl aldehyde, Pelargonaldehyde

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About This Item

Linear Formula:
CH3(CH2)7CHO
CAS Number:
Molecular Weight:
142.24
Beilstein:
1236701
EC Number:
MDL number:
UNSPSC Code:
12000000
PubChem Substance ID:

Pricing and availability is not currently available.

grade

analytical standard

Quality Level

vapor pressure

~0.26 mmHg ( 25 °C)

Assay

≥99.5% (GC)

CofA

current certificate can be downloaded

packaging

ampule of 1000 mg

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.424 (lit.)

bp

93 °C/23 mmHg (lit.)

density

0.827 g/mL at 25 °C (lit.)

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This Item
524666169680139
Nonanal analytical standard

442719

Nonanal

Octanal analytical standard

52466

Octanal

Undecanal analytical standard

80139

Undecanal

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

format

neat

format

neat

format

neat

format

neat

grade

analytical standard

grade

analytical standard

grade

analytical standard

grade

analytical standard

storage temp.

2-30°C

storage temp.

-

storage temp.

2-8°C

storage temp.

-

assay

≥99.5% (GC)

assay

≥98.0% (GC)

assay

≥97.0% (GC)

assay

≥98.0% (GC)

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Aquatic Chronic 3 - Skin Irrit. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

147.2 °F - closed cup

Flash Point(C)

64 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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    Thomas Van Hecke et al.
    PloS one, 9(6), e101122-e101122 (2014-07-01)
    The effects of fat content and nitrite-curing of pork were investigated on the formation of cytotoxic and genotoxic lipid oxidation products (malondialdehyde, 4-hydroxy-2-nonenal, volatile simple aldehydes), protein oxidation products (protein carbonyl compounds) and NOC-specific DNA adducts (O6-carboxy-methylguanine) during in vitro
    Zainulabeuddin Syed et al.
    Proceedings of the National Academy of Sciences of the United States of America, 106(44), 18803-18808 (2009-10-28)
    West Nile virus, which is transmitted by Culex mosquitoes while feeding on birds and humans, has emerged as the dominant vector borne disease in North America. We have identified natural compounds from humans and birds, which are detected with extreme
    Seung-Ah Lee et al.
    Biochimica et biophysica acta, 1782(6), 421-425 (2008-04-09)
    Mutations in human Retinol Dehydrogenase 12 (RDH12) are known to cause photoreceptor cell death but the physiological function of RDH12 in photoreceptors remains poorly understood. In vitro, RDH12 recognizes both retinoids and medium-chain aldehydes as substrates. Our previous study suggested
    Ke-Ming Li et al.
    Journal of chemical ecology, 38(3), 287-294 (2012-03-10)
    Odorant receptors are thought to play critical roles in the perception of chemosensory stimuli by insects. The primary method to address the functions of odorant receptors in insects is to use in vitro binding assays between the receptors and potential
    Elena Chiarpotto et al.
    BioFactors (Oxford, England), 24(1-4), 229-236 (2006-01-13)
    Transient activation of fibroblasts or fibroblast-like cells to proliferate and to produce elevated quantities of extracellular matrix is essential to fibrosis. This activation is regulated by several cytokines produced by various inflammation-associated cells. Among these, transforming growth factor beta1 (TGFbeta1)

    Protocols

    Fast GC analysis of sweet orange essential oil in hexane. Key components identified includes: β-Farnesene; α-Huµlene; Germacrene D; (+)-Valencene; Bicyclogermacrene; (+)-δ-Cadinene

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