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O5608

Sigma-Aldrich

Octanal

99%

Synonym(s):

Aldehyde C8, Caprylic aldehyde, Octyl aldehyde

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About This Item

Linear Formula:
CH3(CH2)6CHO
CAS Number:
Molecular Weight:
128.21
Beilstein:
1744086
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor pressure

2 mmHg ( 20 °C)
2 mmHg ( 20 °C)
850 mmHg ( 25 °C)

Quality Level

Assay

99%

refractive index

n20/D 1.421 (lit.)

bp

171 °C (lit.)

mp

12-15 °C (lit.)

density

0.82 g/mL at 25 °C (lit.)

SMILES string

[H]C(=O)CCCCCCC

InChI

1S/C8H16O/c1-2-3-4-5-6-7-8-9/h8H,2-7H2,1H3

InChI key

NUJGJRNETVAIRJ-UHFFFAOYSA-N

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Application

Octanal is an essential precursor in the total synthesis of (−)-dihydrosporothriolide, (+)-tetrahydropyrenophorol and (+)-awajanomycin. It can also be used in the synthesis of erythritol and pentaerythritol based hydrotropes.

Pictograms

FlameExclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

125.6 °F - closed cup

Flash Point(C)

52 °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’.

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Total Synthesis of (?)-Dihydrosporothriolide Utilizing an Indium-Mediated Reformatsky?Claisen Rearrangement.
Ishihara J, et al.
The Journal of Organic Chemistry, 79(12), 5908-5913 (2014)
Asymmetric synthesis of the cytotoxic marine natural product (+)-awajanomycin and its C-11 epimer.
Fu R, et al.
The Journal of Organic Chemistry, 75(12), 4230-4243 (2010)
Roberto Romani et al.
Insects, 10(6) (2019-06-19)
Sitophilus zeamais (Motschulsky) is considered as one of the most destructive foodstuff pests. Due to their efficiency, low toxicity for mammalians and low environmental impact, plant-derived essential oils (EOs) are promising tools for pest control. In particular, the OEs extracted
An eco-compatible pathway to new hydrotropes from tetraols.
Herbinski A A, et al.
Green Chemistry (2018)
Ricardo C Araneda et al.
The Journal of physiology, 555(Pt 3), 743-756 (2004-01-16)
Several lines of evidence suggest that odorants are recognized through a combinatorial process in the olfactory system; a single odorant is recognized by multiple receptors and multiple odorants are recognized by the same receptor. However few details of how this

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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