2-METHYL OCTANAL CAS 7786-29-0

Introduction:Basic information about 2-METHYL OCTANAL CAS 7786-29-0, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

2-METHYL OCTANAL Basic information

Product Name:2-METHYL OCTANAL
Synonyms:2-METHYL OCTANAL;METHYL HEXYL ACETALDEHYDE;FEMA 2727;2-methyl-octana;alpha-methyloctanal;Octanal, 2-methyl-;METHYLHEXYLACETALDEHYD;2-Methyloctanal?New
CAS:7786-29-0
MF:C9H18O
MW:142.24
EINECS:232-093-0
Product Categories:
Mol File:7786-29-0.mol

2-METHYL OCTANAL Chemical Properties

Melting point -18°C (estimate)
Boiling point 189.85°C (estimate)
density 0.8410
FEMA 2727 | 2-METHYLOCTANAL
refractive index 1.4230
storage temp. Inert atmosphere,Store in freezer, under -20°C
solubility Insoluble in water, soluble in alcohol and oils.
form Colourless oily liquid.
Odorat 100.00 %. floral rose lily muguet
Odor Typefloral
JECFA Number270
Cosmetics Ingredients FunctionsPERFUMING
LogP3.38
EPA Substance Registry SystemOctanal, 2-methyl- (7786-29-0)

Safety Information

TSCA TSCA listed

2-METHYL OCTANAL Usage And Synthesis

Description2-Methyloctanal has a delicate, floral odor (rose- or lily-like).Prepared by heating methoxymethyl hexyl carbinol with oxalicacid or with anhydrous formic acid; also from hexanal and propionicaldehyde, Darzen’s synthesis of reacting methyl hexyl ketoneand ethyl chloroacetate with sodium ethylate; the resulting esteris then hydrolyzed to the acid and this heated under vacuum.
Chemical Properties2-Methyloctanal has a delicate, floral odor, rose- or lily-like
UsesIn effect more versatile than Methyl nonyl acetaldehyde, 2-methyloctanal creates floral-diffusive topnotes in a Lily or Muguet, freshness in Mimosa or Rose, gives clean and airy topnotes to Citrus fragrances, etc. It finds some use in flavor compositions, mainly in Citrus types where it may partly or wholly substitute the conventional Nonanal. Concentration used is about 1 to 2 ppm in the finished product.
DefinitionChEBI: 2-Methyloctanal is a fatty aldehyde.
Safety ProfileLow toxicity byingestion and skin contact. A skin irritant.When heated to decomposition it emitsacrid smoke and irritating fumes.
SynthesisBy heating methoxymethyl hexyl carbinol with oxalic acid or with anhydrous formic acid; also from hexanal and propionic aldehyde, Darzen’s synthesis of reacting methyl hexyl ketone and ethyl chloroacetate with sodium ethylate; the resulting ester isthen hydrolyzed to the acid and this heated under vacuum.

2-METHYL OCTANAL Preparation Products And Raw materials

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