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106-70-7
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???(??):
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Methyl hexanoate
???(??):
METHYL CAPROATE;HEXANOIC ACID METHYL ESTER;METHYL HEXOATE;METHYL AMYL ACETATE;HEXANOIC METHYL;CAPROIC ACID METHYL ESTER;FEMA 2708;METHYLCAPRONAT;methylhexylate;Methyl hexylate
CBNumber:
CB6755858
???:
C7H14O2
??? ??:
130.18
MOL ??:
106-70-7.mol
MSDS ??:
SDS

??????????? ??

???
-71 °C (lit.)
?? ?
151 °C (lit.)
??
0.885 g/mL at 25 °C (lit.)
???
3.7 hPa (20 °C)
FEMA
2708 | METHYL HEXANOATE
???
n20/D 1.405
???
113 °F
?? ??
Store below +30°C.
???
?????: ???100mg/mL, ??
??? ??
??
??
???
??
100.00%??. ??? ?? ???? ?? ?? ?? ?? ??? ???
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synthetic
???
1.325g/L(20℃)
JECFA Number
1871
BRN
1744683
Dielectric constant
4.7000000000000002
???
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LogP
2.34
CAS ??????
106-70-7(CAS DataBase Reference)
NIST
Hexanoic acid, methyl ester(106-70-7)
EPA
Methyl hexanoate (106-70-7)
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  • ?? ? ?? ??
  • ?? ? ???? ?? (GHS)
?? ???? ?? 10
????? 43-16-36/37/39-7
????(UN No.) UN 3272 3/PG 3
WGK ?? 1
RTECS ?? MO8401400
TSCA Yes
?? ?? 3
???? III
HS ?? 29159080
?? LD50 orally in Rabbit: > 5000 mg/kg
???? ?? KE-24223
????(GHS): GHS hazard pictograms
?? ?: Warning
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?? ??·?? ?? ?? ?? ?? ?? ? ?? ?? P- ??
H226 ??? ?? ? ?? ??? ?? ?? 3 ??
??????:
P210 ?·???·??·????? ????? - ?? ???.
NFPA 704
2
1 0

??????????? MSDS


Methyl hexanoate

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Methyl hexanoate has an ether-like odor reminiscent of pineapple. May be prepared by reacting methyl alcohol with hexanoic acid at 130 - 140°C in the presence of concentrated H2S04 and distilling the ester from the reaction mixture.

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Methyl hexanoate has an ether-like odor reminiscent of pineapple

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Reported found in pineapple, apple, apricot, orange juice, black currants, guava, grapes, melon, papaya, pineapple, raspberry, blackberry, strawberry, potato, tomato, pepper, rye bread, cheeses, butter, milk, beef mutton, hop oil, beer, grape wine, cider, coffee, tea, honey, cloudberry, durian (Durio zibethinus), olive, passion fruit, plumcot, mushroom, starfruit, mango, wood apple, licorice, soursop, cashew apple, wort, cherimoya, kiwifruit, babaco fruit (Carica pentagona Heilborn), Bourbon vanilla, mountain papaya, oyster, custard apple, nectarine, naranjilla, lamb’s lettuce, loganberry, cape gooseberry, spineless monkey orange, Chinese quince and pawpaw.

??

Intermediate for caproic acid detergents, emulsifiers, wetting agents, stabilizers, resins, lubricants, plasticizers, flavoring.

?? ??

By reacting methyl alcohol with hexanoic acid at 130 to 140°C in the presence of concentrated H2SO4 and distilling the ester from the reaction mixture

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ChEBI: A fatty acid methyl ester derived from hexanoic (caproic acid).

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Clear colorless liquid.

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Insoluble in water.

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Methyl hexanoate is an ester. Esters react with acids to liberate heat along with alcohols and acids. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Heat is also generated by the interaction of esters with caustic solutions. Flammable hydrogen is generated by mixing esters with alkali metals and hydrides. Methyl hexanoate reacts with strong oxidizing agents and strong bases.

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Methyl hexanoate is combustible.

Synthesis

Methyl caproate is synthesized by direct esterification of n-Caproic (n-Hexanoic) acid with Methanol, preferably under azeotropic conditions.

Purification Methods

Pass it through alumina and distil it before use. [Beilstein 2 IV 921.]

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