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2-METHYL OCTANAL

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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
Mol File:
7786-29-0.mol
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2-METHYL OCTANAL Chemical Properties

Melting point:
-18°C (estimate)
Boiling point:
189.85°C (estimate)
Density 
0.8410
refractive index 
1.4230
FEMA 
2727 | 2-METHYLOCTANAL
storage temp. 
Inert atmosphere,Store in freezer, under -20°C
solubility 
Insoluble in water, soluble in alcohol and oils.
form 
Colourless oily liquid.
Odor
at 100.00 %. floral rose lily muguet
Odor Type
floral
JECFA Number
270
LogP
3.38
EPA Substance Registry System
Octanal, 2-methyl- (7786-29-0)
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2-METHYL OCTANAL Usage And Synthesis

Description

2-Methyloctanal has a delicate, floral odor (rose- or lily-like). Prepared by 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 is then hydrolyzed to the acid and this heated under vacuum.

Chemical Properties

2-Methyloctanal has a delicate, floral odor, rose- or lily-like

Uses

In 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.

Definition

ChEBI: 2-Methyloctanal is a fatty aldehyde.

Safety Profile

Low toxicity by ingestion and skin contact. A skin irritant. When heated to decomposition it emits acrid smoke and irritating fumes.

Synthesis

By 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 is then hydrolyzed to the acid and this heated under vacuum.

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