Description References
ChemicalBook > CAS DataBase List > Methyl hexanoate

Methyl hexanoate

Description References
Product Name
Methyl hexanoate
CAS No.
106-70-7
Chemical Name
Methyl hexanoate
Synonyms
METHYL CAPROATE;HEXANOIC ACID METHYL ESTER;METHYL HEXOATE;METHYL AMYL ACETATE;HEXANOIC METHYL;CAPROIC ACID METHYL ESTER;FEMA 2708;methylhexylate;METHYLCAPRONAT;Methyl hexylate
CBNumber
CB6755858
Molecular Formula
C7H14O2
Formula Weight
130.18
MOL File
106-70-7.mol
More
Less

Methyl hexanoate Property

Melting point:
-71 °C (lit.)
Boiling point:
151 °C (lit.)
Density 
0.885 g/mL at 25 °C (lit.)
vapor pressure 
3.7 hPa (20 °C)
FEMA 
2708 | METHYL HEXANOATE
refractive index 
n20/D 1.405
Flash point:
113 °F
storage temp. 
Store below +30°C.
solubility 
chloroform: soluble100mg/mL, clear
form 
Liquid
color 
Colorless
Odor
at 100.00 %. ethereal fruity pineapple apricot strawberry tropical fruit banana bacon
Odor Type
fruity
Water Solubility 
1.325g/L(20 ºC)
JECFA Number
1871
BRN 
1744683
Dielectric constant
4.7000000000000002
Stability:
Stable. Flammable. Incompatible with strong oxidizing agents, strong bases.
LogP
2.34
CAS DataBase Reference
106-70-7(CAS DataBase Reference)
NIST Chemistry Reference
Hexanoic acid, methyl ester(106-70-7)
EPA Substance Registry System
Methyl hexanoate (106-70-7)
More
Less

Safety

Risk Statements 
10
Safety Statements 
43-16-36/37/39-7
RIDADR 
UN 3272 3/PG 3
WGK Germany 
1
RTECS 
MO8401400
TSCA 
Yes
HazardClass 
3
PackingGroup 
III
HS Code 
29159080
Toxicity
LD50 orally in Rabbit: > 5000 mg/kg
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H226Flammable liquid and vapour

Precautionary statements

P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
W270814
Product name
Methyl hexanoate
Purity
natural, ≥99%, FG
Packaging
100g
Price
$115
Updated
2024/03/01
Sigma-Aldrich
Product number
W270814
Product name
Methyl hexanoate
Purity
natural, ≥99%, FG
Packaging
1kg
Price
$675
Updated
2024/03/01
Sigma-Aldrich
Product number
W270814
Product name
Methyl hexanoate
Purity
natural, ≥99%, FG
Packaging
4kg
Price
$1670
Updated
2024/03/01
Sigma-Aldrich
Product number
PHR3533
Product name
Methyl Hexanoate
Purity
pharmaceutical secondary standard, certified reference material
Packaging
1G
Price
$259
Updated
2024/03/01
Sigma-Aldrich
Product number
8.20638
Product name
Methyl hexanoate
Purity
for synthesis
Packaging
5ml
Price
$24.6
Updated
2024/03/01
More
Less

Methyl hexanoate Chemical Properties,Usage,Production

Description

Methyl hexanoate is the methyl ester form of hexanoate with fruity type odor and flavor. It is formed by the esterification between methanol and hexanoate. It can be found in many sources such as wine grapes, melon, raspberry, blackberry, plum, quince, apple brandy, wines, Bourbon vanilla, coffee, black tea, potato, tomato, cheeses, rye bread, meats and other foodstuffs. Its major application is used as cosmetic, flavor and fragrance agents.

References

Arora, D. K., A. P. Hansen, and M. S. Armagost. "Sorption of flavor compounds by low density polyethylene film." Journal of food science 56.5 (1991): 1421-1423.
Wohlfarth, Ch. "Refractive index of methyl hexanoate." Refractive Indices of Pure Liquids and Binary Liquid Mixtures (Supplement to III/38). Springer Berlin Heidelberg, 2008. 414-414.
Glaude, Pierre Alexandre, et al. "Modeling of the oxidation of methyl esters—Validation for methyl hexanoate, methyl heptanoate, and methyl decanoate in a jet-stirred reactor." Combustion and flame 157.11 (2010): 2035-2050.

Description

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.

Chemical Properties

Methyl hexanoate has an ether-like odor reminiscent of pineapple

Chemical Properties

colourless liquid

Occurrence

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.

Uses

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

Preparation

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

Definition

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

Aroma threshold values

Detection: 10 to 87 ppb

Synthesis Reference(s)

Tetrahedron, 35, p. 2169, 1979 DOI: 10.1016/0040-4020(79)87035-0
Tetrahedron Letters, 30, p. 2945, 1989 DOI: 10.1016/S0040-4039(00)99165-2

General Description

Clear colorless liquid.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

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.

Fire Hazard

Methyl hexanoate is combustible.

Flammability and Explosibility

Flammable

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.]

Methyl hexanoate Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

Methyl hexanoate Suppliers

HBCChem, Inc.
Tel
+1-510-219-6317
Fax
+1-650-486-1361
Email
sales@hbcchem.com
Country
United States
ProdList
10648
Advantage
60
Aladdin Scientific
Tel
+1-+1(833)-552-7181
Email
sales@aladdinsci.com
Country
United States
ProdList
57505
Advantage
58
Cayman Chemical Company
Tel
--
Fax
--
Email
cayman@caymanchem.com
Country
United States
ProdList
6213
Advantage
81
Synerzine, Inc. (formerly Pyrazine Specialties, Inc. and CTC Organics)
Tel
--
Fax
--
Email
info@synerzine.com
Country
United States
ProdList
314
Advantage
58
Advanced Organic Synthesis, LLC (AOS).
Tel
--
Fax
--
Email
sales@aosynthesis.com
Country
United States
ProdList
120
Advantage
58
Fleurchem Inc.,
Tel
--
Fax
--
Country
United States
ProdList
119
Advantage
58
Advanced Biotech - ABT
Tel
--
Fax
--
Country
United States
ProdList
260
Advantage
58
WEN International Inc.
Tel
--
Fax
--
Country
United States
ProdList
86
Advantage
58
P&G Chemicals
Tel
--
Fax
--
Country
United States
ProdList
12
Advantage
58
Auro Chemicals
Tel
--
Fax
--
Email
customerservice@aurochemicals.com
Country
United States
ProdList
246
Advantage
58
H.Interdonati inc.
Tel
--
Fax
--
Email
flavorplus@aol.com
Country
United States
ProdList
105
Advantage
58
PearlChem Corporation
Tel
--
Fax
--
Email
info@pearlchemcorp.com
Country
United States
ProdList
131
Advantage
58
Lluch Essence S.L.
Tel
--
Fax
--
Email
web@lluche.com
Country
United States
ProdList
2352
Advantage
58
Taytonn ASCC Pte Ltd
Tel
--
Fax
--
Email
info@taytonnascc.com
Country
United States
ProdList
742
Advantage
58
Berje Inc.
Tel
--
Fax
--
Email
tlauzurica@berjeinc.com
Country
United States
ProdList
958
Advantage
58
Frutarom (F&F Ingredients)
Tel
--
Fax
--
Email
info@frutarom.com
Country
United States
ProdList
280
Advantage
58
H.Interdonati, Inc. & FlavorPlus Division
Tel
--
Fax
--
Country
United States
ProdList
25
Advantage
58
Oakwood Products, Inc.
Tel
--
Fax
--
Email
sales@oakwoodchemical.com
Country
United States
ProdList
6193
Advantage
74
Vigon International, Inc.
Tel
--
Fax
--
Email
jpassamonte@vigoninternational.com
Country
United States
ProdList
1268
Advantage
64
United States Biological
Tel
--
Fax
--
Email
chemicals@usbio.net
Country
United States
ProdList
6214
Advantage
80
Charkit Chemical Corporation
Tel
--
Fax
--
Email
sales@charkit.com
Country
United States
ProdList
2993
Advantage
65
Pyrazine Specialties, Inc.
Tel
--
Fax
--
Country
United States
ProdList
1265
Advantage
30
Vigon International
Tel
--
Fax
--
Email
sales@vigon.com
Country
United States
ProdList
1776
Advantage
58
Indukern, S.A. F&F Ingredients Division
Tel
--
Fax
--
Email
info@indukern.es
Country
United States
ProdList
1321
Advantage
58
NATURAL ADVANTAGE
Tel
--
Fax
--
Email
customerservice@natural-advantage.net
Country
United States
ProdList
401
Advantage
51
M&U International LLC
Tel
--
Fax
--
Email
sales@mu-intel.com
Country
United States
ProdList
2011
Advantage
58
Sunaux International
Tel
--
Fax
--
Email
johnjft@sunaux.com
Country
United States
ProdList
581
Advantage
58
Advanced Biotech. Inc.
Tel
--
Fax
--
Email
info@adv-bio.com
Country
United States
ProdList
1121
Advantage
58
Ernesto Ventós S.A.
Tel
--
Fax
--
Email
info@ventos.com
Country
United States
ProdList
2257
Advantage
58
Penta International Corporation
Tel
--
Fax
--
Email
lisaa@pentamfg.com
Country
United States
ProdList
5042
Advantage
58
R C Treatt and Co Ltd
Tel
--
Fax
--
Email
enquiries@treatt.com
Country
United States
ProdList
1690
Advantage
58
Excellentia International
Tel
--
Fax
--
Email
info@excellentiaint.com
Country
United States
ProdList
567
Advantage
58
FRUTAROM USA INC,
Tel
--
Fax
--
Email
Sales.IFFIngredients@iff.com
Country
United States
ProdList
500
Advantage
58
Fleurchem, Inc.
Tel
--
Fax
--
Email
info@fleurchem.com
Country
United States
ProdList
790
Advantage
58
Moellhausen S.P.A.
Tel
--
Fax
--
Country
United States
ProdList
1676
Advantage
58
Anhui Primechem
Tel
--
Fax
--
Email
henry@primekem.com
Country
United States
ProdList
71
Advantage
58
Alfrebro LLC/ Archer Daniels Midland Company
Tel
--
Fax
--
Email
sforbis@alfrebro.com
Country
United States
ProdList
768
Advantage
58
H. Interdonati, Inc.
Tel
--
Fax
--
Email
flavorplus@hinterdonati.com
Country
United States
ProdList
261
Advantage
58
TCI America
Tel
--
Fax
--
Email
sales@tciamerica.com
Country
United States
ProdList
6909
Advantage
75
Riedel-de Haen AG
Tel
--
Fax
--
Country
United States
ProdList
6773
Advantage
87
HBCChem Inc.
Tel
--
Fax
--
Email
sales@hbcchem-inc.com
Country
United States
ProdList
4569
Advantage
30
Waterstone Technology, LLC
Tel
--
Fax
--
Email
sales@waterstonetech.com
Country
United States
ProdList
6786
Advantage
30
ChemService Inc.
Tel
--
Fax
--
Country
United States
ProdList
6379
Advantage
68
Penta Manufacturing Company
Tel
--
Fax
--
Email
sales@pentamfg.com
Country
United States
ProdList
5076
Advantage
65
SRS Aromatics Ltd
Tel
--
Fax
--
Email
info@srsaromatics.co.uk
Country
United States
ProdList
2315
Advantage
46
INDOFINE Chemical Company, Inc.
Tel
--
Fax
--
Email
chemical@indofinechemical.com
Country
United States
ProdList
6176
Advantage
69
Advance Scientific & Chemical
Tel
--
Fax
--
Email
sales@advance-scientific.com
Country
United States
ProdList
6419
Advantage
71
City Chemical LLC
Tel
--
Fax
--
Email
sales@citychemical.com
Country
United States
ProdList
6708
Advantage
72
3B Scientific Corporation
Tel
--
Fax
--
Email
sales@3bsc.com
Country
United States
ProdList
6718
Advantage
47
HONEST JOY HOLDINGS LIMITED
Tel
--
Fax
--
Email
sales@honestjoy.cn
Country
United States
ProdList
6675
Advantage
54
More
Less

View Lastest Price from Methyl hexanoate manufacturers

Career Henan Chemical Co
Product
Methyl hexanoate 106-70-7
Price
US $80.00/KG
Min. Order
1KG
Purity
1
Supply Ability
1000KG
Release date
2018-08-04

106-70-7, Methyl hexanoateRelated Search:


  • C6:0 METHYL ESTER
  • FEMA 2708
  • HEXANOIC ACID METHYL ESTER
  • METHYL HEXANOATE
  • METHYL HEXOATE
  • METHYL N-HEXANOATE
  • METHYL N-CAPROATE
  • METHYL CAPROATE
  • METHYL CAPRONATE
  • Methyl ester of hexanoic acid
  • Methyl hexylate
  • Methyl n-hexoate
  • methylhexylate
  • RARECHEM AL BF 0164
  • N-CAPROIC ACID METHYL ESTER
  • Methyl hexanoate, 99.5%
  • Caproic acid methyl ester Methyl caproate Hexanoic Acid Methyl Ester
  • CAPROIC ACID METHYL ESTER
  • Natural Methyl Caproate
  • Natural Methyl Hexanoate
  • METHYL AMYL ACETATE
  • METHYL HEXANOATE 99+% NATURAL
  • METHYL CAPROATE, STANDARD FOR GC
  • METHYL HEXANOATE 99+%
  • METHYL HEXANOATE OEKANAL
  • Caproicacidmethylester=Methylhexanoate
  • CAPROIC ACID METHYLESTER(SG)
  • CAPROIC ACID METHYLESTER WITH GC
  • Methyl Hexanoate [Standard Material]
  • METHYL CAPROATE, NATURAL
  • Caproic acid methyl ester, Methyl caproate
  • METHYLCAPRONAT
  • Hexanoic acid methyl
  • Methyl hexanoate (Methyl caproate)
  • Methyl hexanoate >=99.0%
  • Methyl Hexanoate [Standard Material for GC]
  • Methyl hexanoate,Caproic acid methyl ester, Methyl caproate
  • Methyl Caproate (300 mg)
  • METHYL CAPROATE, 99.5% (GLC)
  • Methyl hexanoate, 98% 5GR
  • Methyl hexanoate,98%
  • Methyl hexanoate (C6:0)
  • Methyl hexanoate (C6:0) Solution
  • Methyl hexanoate 99%
  • MethylCaproate/MethylHexanoate(C6:0)
  • MethylHexanoate[StandardMaterialforGC]&gt
  • MethylHexanoate&gt
  • METHYL HEXANOATE FOR SYNTHESIS
  • Methyl hexanoate USP/EP/BP
  • HEXANOIC METHYL
  • Methyl hexanoate(kosher)
  • C6:0 Caproic acid methyl ester
  • C6:0 Hexanoic(Caproic) Acid Methyl Ester
  • Caproic Acid Methylester(AS)
  • C14196400 HexanoiCacid-methyLester
  • C6:0 Caproic acid methyl ester in Heptane
  • 106-70-7
  • CH3CH24CO2CH3