Tetradecanal
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Tetradecanal
structure -
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CAS No:
124-25-4
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Formula:
C14H28O
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Chemical Name:
Tetradecanal
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Synonyms:
Tetradecanal;Myristaldehyde;n-Tetradecyl aldehyde;Myristylaldehyde;Tetradecyl aldehyde;n-Tetradecanal;Tetradecanaldehyde;1-Tetradecanal;Myristinaldehyde;NSC 66435;Aldehyde peche (C14);Peach aldehyde (C14);511542-15-7
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CAS No:
Description
Myristaldehyde has a strong, fatty, orris-like odor and a sweet, fatty, “citrus-peel” flavor (diluted) White Semi-SolidChEBI: A long-chain fatty aldehyde that is tetradecane in which two hydrogens attached to a terminal carbon are replaced by an oxo group. It is found in coriander.Myristaldehyde has a strong, fatty, orris-like odor with a sweet, fatty, “citrus-peel” flavor (diluted). Industrially prepared from the corresponding myristic acid.
Solid|colourless to pale yellow liquid/fatty, orris-like odour
Tetradecanal is a long-chain fatty aldehyde that is tetradecane in which two hydrogens attached to a terminal carbon are replaced by an oxo group. It is found in coriander. It has a role as a bacterial metabolite and a plant metabolite. It is a long-chain fatty aldehyde and a 2,3-saturated fatty aldehyde. It derives from a hydride of a tetradecane.
Characteristics
17.1
6
colorless to pale yellow solid
0.8278
26-27 °C
166 °C @ Press: 24 Torr
121.5ºC
1.441
0.4852 mg/L @ 25 °C (est)|soluble inmost organic solvents; Insoluble in water|1 ml in 1 ml of 80% alcohol (in ethanol)
The acute oral LD 50 value was reported as > 5Og/kg in the rat . The acute dermal LD 50 for sample no. 71-17 was reported to be > 10 g/kg
Safety Information
36/37/38
26-37/39
XB7900000
Xi
P264, P280, P302+P352, P305+P351+P338, P321, P332+P313, P337+P313, P362
H315
|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P264, P280, P302+P352, P305+P351+P338, P321, P332+P313, P337+P313, and P362|Aggregated GHS information provided by 1461 companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Tetradecanal Use and Manufacturing
Derived from the oxidation of myristyl alcohol. It can also be obtained by the reduction of myristic acid. Boiling point is 260℃. Natural products exist in kumquat peel, cucumber, ginger, etc.
A major component of the essential oil found in the leaves of Azadirachta indica.
Tetradecanal: ACTIVE
Food additives -> Flavoring Agents|Flavoring Agents -> JECFA Flavorings Index|Fatty Acyls [FA] -> Fatty aldehydes [FA06]
Flavoring Agents
Computed Properties
Molecular Weight:212.37
XLogP3:6
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:12
Exact Mass:212.214015512
Monoisotopic Mass:212.214015512
Topological Polar Surface Area:17.1
Heavy Atom Count:15
Complexity:121
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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