Basic information
- Standard SMILES
CCCCCCOC(C)=O- InChIKey
AOGQPLXWSUTHQB-UHFFFAOYSA-N- Molecular formula
- C8H16O2
- Average molar mass
- 144.21 g/mol
- Monoisotopic mass
- 144.11502975
Overview
Hexyl acetate appears as a colorless liquid with a mild sweet odor. Flash point 113 °F. A moderate fire risk. Inhalation may cause adverse effects. Insoluble in water and very soluble in alcohols and ethers. When heated to high temperatures emits acrid smoke and fumes. Used as a solvent and as a propellant in aerosols.
Names & identifiers
- Preferred name
- Hexyl Acetate
- IUPAC
- hexyl acetate
- English name
- Hexyl acetate
- Molecular formula
- C8H16O2
- Molecular weight
- 144.21
Names & synonyms
Show more names
Database identifiers
- CAS
142-92-7、88230-35-7- PubChem CID
- 8908
- DTXSID
DTXSID6022006- ChEMBL
CHEMBL2228454- ChEBI
CHEBI:87510- UNII
- 7U7KU3MWT0
- EC Number
- 205-572-7
- Nikkaji
- J2.028A
Properties
Computed structural properties
- XLogP
- 2.4
- Topological polar surface area
- 26.3 Ų
- Hydrogen bond donors
- 0
- Hydrogen bond acceptors
- 2
- Rotatable bonds
- 6
- Heavy atoms
- 10
- Formal charge
- 0
- Complexity
- 89.3
Experimental & physicochemical properties
Odor
Sweet-fruity, pearl-like odor
Sweet ester odor
Density
0.876 (USCG, 1999) - Less dense than water; will float
0.8779 g/cu cm at 15 °C
0.868-0.872
Solubility
Very soluble in alcohol and ether
In water, 511 mg/L at 25 °C
0.511 mg/mL at 25 °C
soluble in alcohol, ether; insoluble in water
1 ml in 1 ml 95% alcohol (in ethanol)
Physicochemical properties
- Melting point
- -80 °C · -80 °C (lit.)
- Boiling point
- 168 · 168-170 °C (lit.)
- Density
- 0.87 g/mL · 0.87 g/mL at 25 °C (lit.)
- vapor pressure
- 5 hPa · 5 hPa (20 °C)
- FEMA
- 2565 · 2565 | HEXYL ACETATE
- refractive index
- 20 · n20/D 1.409(lit.)
- FLAVIS Number
- 9.006 · 09.006 | Hexyl acetate
- Flash point
- 99 °F · 99 °F
- storage temp.
- 30 °C · Store below +30°C.
- solubility
- 0.4 g/l · 0.4g/l
- form
- Liquid
- color
- Clear colorless to pale yellow
- Odor
- 10 % · at 10.00 % in dipropylene glycol. fruity green apple banana sweet
- Odor Type
- fruity
- biological source
- synthetic
- Odor Threshold
- 0.0018 ppm · 0.0018ppm
- Water Solubility
- immiscible
- Specific Heat Capacity
- 1.96 J/ · Cp(liquid): 1.96 J/(g·K), at 25℃
- Thermal Conductivity
- 0.129 W/ · 0.129 W/(m·K) at 25 ℃
- JECFA Number
- 128 · 128
- BRN
- 1747138 · 1747138
- Henry's Law Constant
- 2 · 2.0×10-2 mol/(m3Pa) at 25℃, Brockbank (2013)
- Dielectric constant
- 4.42 · 4.4199999999999999
- Major Application
- flavors and fragrances
- Cosmetics Ingredients Functions
- PERFUMINGFLAVOURINGFRAGRANCE
- InChI
- 1S/C8H16O2/c1-3-4-5-6-7-10-8(2)9/h3-7H2,1-2H3
- InChIKey
- AOGQPLXWSUTHQB-UHFFFAOYSA-N
- SMILES
- CCCCCCOC(C)=O
- LogP
- 3.3 at · 3.3 at 30℃
- Surface tension
- 26.75 mN/m · 26.75mN/m at 298.15K
- CAS DataBase Reference
- 142 · 142-92-7(CAS DataBase Reference)
- Substances Added to Food (formerly EAFUS)
- HEXYL ACETATE
- FDA 21 CFR
- 172.515 · 172.515
- EWG's Food Scores
- 1 · 1
- FDA UNII
- 7 U7KU3MWT0 · 7U7KU3MWT0
- NIST Chemistry Reference
- Hexyl ethanoate(142-92-7)
- EPA Substance Registry System
- Acetic acid, hexyl ester (142-92-7)
- UNSPSC Code
- 85151701 · 85151701
- NACRES
- 24 · NA.24
- Symbol(GHS)
- 2 · GHS02,GHS07
- Signal word
- Warning
- Hazard statements
- 315 · H315+H320-H335-H226
- Precautionary statements
- 501 · P501-P240-P261-P210-P233-P243-P241-P242-P271-P264-P280-P370+P378-P337+P313-P305+P351+P338-P362+P364-P303+P361+P353-P332+P313-P304+P340+P312-P403+P233-P403+P235-P405
- PPE
- Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
- Risk Statements
- 10 · 10
- Safety Statements
- 16 · 16
- RIDADR
- 3272 · UN 3272 3/PG 3
- WGK Germany
- 1 · 1
- RTECS
- 875000 · AI0875000
- TSCA
- TSCA listed
- HazardClass
- 3 · 3
- PackingGroup
- III
- HS Code
- 29153990 · 29153990
- Storage Class
- 3 · 3 - Flammable liquids
- Hazard Classifications
- 2 Flam · Aquatic Chronic 2Flam. Liq. 3
- Hazardous Substances Data
- 142 · 142-92-7(Hazardous Substances Data)
- Toxicity
- 50 orally · LD50 orally in Rabbit: 36100 mg/kg LD50 dermal Rabbit > 5000 mg/kg
- REACH Registrations
- Active
Safety & regulation
GHS classification
GHS Classification
This chemical does not meet GHS hazard criteria for 0.4% (8 of 1939) of reports.
Warning
H226 (98%): Flammable liquid and vapor [Warning Flammable liquids]
P210, P233, P240, P241, P242, P243, P273, P280, P303+P361+P353, P370+P378, P391, P403+P235, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 1939 reports by companies from 12 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Warning
Hazard information
Regulatory Information
Chemical: Acetic acid, hexyl ester
Regulation (EC) No 1831/2003 (amended)
Acetic acid, hexyl ester is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Acetic acid, hexyl ester are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)
Status: Active Update: 31-03-2023 https://echa.europa.eu/registration-dossier/-/registered-dossier/13766
Hexyl acetate: Does not have an individual approval but may be used under an appropriate group standard
Reactivity Profile
HEXYL ACETATE 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.
Safety & protection
Fire Fighting Procedures
If material on fire or involved in fire: Do not extinguish fire unless flow can be stopped. Use water in flooding quantities as fog. Solid streams of water may be ineffective. Cool all affected containers with flooding quantities of water. Apply water from as far a distance as possible. Use "alcohol" foam, dry chemical or carbon dioxide.
Disposal Methods
SRP: The most favorable course of action is to use an alternative chemical product with less inherent propensity for occupational harm/injury/toxicity or environmental contamination. Recycle any unused portion of the material for its approved use or return it to the manufacturer or supplier. Ultimate disposal of the chemical must consider: the material's impact on air quality; potential migration in soil or water; effects on animal and plant life; and conformance with environmental and public health regulations.
Preventive Measures
SRP: The scientific literature for the use of contact lenses by industrial workers is inconsistent. The benefits or detrimental effects of wearing contact lenses depend not only upon the substance, but also on factors including the form of the substance, characteristics and duration of the exposure, the uses of other eye protection equipment, and the hygiene of the lenses. However, there may be individual substances whose irritating or corrosive properties are such that the wearing of contact lenses would be harmful to the eye. In those specific cases, contact lenses should not be worn. In any event, the usual eye protection equipment should be worn even when contact lenses are in place.
If material not on fire and not involved in fire: Keep sparks, flames, and other sources of ignition away. Keep material out of water sources and sewers. Build dikes to contain flow as necessary. Use water spray to knock-down vapors.
Personnel protection: Avoid breathing vapors. Keep upwind. ... Do not handle broken packages unless wearing appropriate personal protective equipment. Wash away any material which may have contacted the body with copious amounts of water or soap and water.
Personal Protective Equipment (PPE)
Excerpt from ERG Guide 128 [Flammable Liquids (Water-Immiscible)]:
Personnel protection: ... Wear appropriate chemical protective gloves, boots, and goggles. Wear positive pressure self-contained breathing apparatus.
Toxicology
Ecotoxicity Values
EC50; Species: Pimephales promelas (Fathead Minnow) age 30-31 days, length 19 mm, weight 0.094 g; Conditions: freshwater, flow through, 24.2 (22.5-25.2) °C, pH 7.7 (7.6-7.8), hardness 42.4 mg/L CaCO3, alkalinity 42.0 mg/L CaCO3, dissolved oxygen 84.4 (72.9-91.6) mg/L; Concentration: 5900 ug/L for 24 hr; Effect: behavior, decreased equilibrium
EC50; Species: Pimephales promelas (Fathead Minnow) age 30-31 days, length 19 mm, weight 0.094 g; Conditions: freshwater, flow through, 24.2 (22.5-25.2) °C, pH 7.7 (7.6-7.8), hardness 42.4 mg/L CaCO3, alkalinity 42.0 mg/L CaCO3, dissolved oxygen 84.4 (72.9-91.6) mg/L; Concentration: 4500 ug/L for 48 hr; Effect: behavior, decreased equilibrium
LC50; Species: Pimephales promelas (Fathead Minnow) age 30-31 days, length 19 mm, weight 0.094 g; Conditions: freshwater, flow through, 24.2 (22.5-25.2) °C, pH 7.7 (7.6-7.8), hardness 42.4 mg/L CaCO3, alkalinity 42.0 mg/L CaCO3, dissolved oxygen 84.4 (72.9-91.6) mg/L; Concentration: 6100 ug/L for 24 hr
LC50; Species: Pimephales promelas (Fathead Minnow) age 30-31 days, length 19 mm, weight 0.094 g; Conditions: freshwater, flow through, 24.2 (22.5-25.2) °C, pH 7.7 (7.6-7.8), hardness 42.4 mg/L CaCO3, alkalinity 42.0 mg/L CaCO3, dissolved oxygen 84.4 (72.9-91.6) mg/L; Concentration: 4800 ug/L for 48 hr
LC50; Species: Pimephales promelas (Fathead Minnow) age 30-31 days, length 19.3 mm, weight 0.094 g; Conditions: freshwater, flow through, 24.9 °C, pH 7.7, hardness 42.4 mg/L CaCO3, alkalinity 42.0 mg/L CaCO3, dissolved oxygen 7.0 mg/L; Concentration: 4000 ug/L for 96 hr (95% confidence interval: 3700-4400 ug/L) /99% purity/
Environmental Fate
TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 62(SRC), determined from a structure estimation method(2), indicates that n-hexyl acetate is expected to have high mobility in soil(SRC). Volatilization of n-hexyl acetate from moist soil surfaces is expected to be an important fate process(SRC) given a Henry's Law constant of 5.3X10-4 atm-cu m/mole(3). n-Hexyl acetate is expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 1.32 mm Hg at 25 °C(4). Although biodegradation data were not available for n-hexyl acetate(SRC, 2011), studies on structurally similar compounds(5-7) have shown that, in general, alkyl acetates are biodegradable(SRC).
AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 62(SRC), determined from a structure estimation method(2), indicates that n-hexyl acetate is expected to adsorb to suspended solids and sediment(SRC). Volatilization from water surfaces is expected(3) based upon a Henry's Law constant of 5.3X10-4 atm-cu m/mole(4). Using this Henry's Law constant and an estimation method(3), volatilization half-lives for a model river and model lake are 5.5 hours and 5.4 days, respectively(SRC). According to a classification scheme(5), an estimated BCF of 34(SRC), from an estimated log Kow of 2.83(6) and a regression-derived equation(7), suggests the potential for bioconcentration in aquatic organisms is moderate(SRC). Hydrolysis is expected to occur slowly based upon estimated hydrolysis half-lives of 2 years and 78 days at pH 7 and 8, respectively(8). Although biodegradation data were not available for n-hexyl acetate(SRC, 2011), studies on structurally similar compounds(9-11) have shown that, in general, alkyl acetates are biodegradable(SRC).
ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), n-hexyl acetate, which has a vapor pressure of 1.32 mm Hg at 25 °C(2), is expected to exist solely as a vapor in the ambient atmosphere. Vapor-phase n-hexyl acetate is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to be 2.2 days(SRC), calculated from its rate constant of 7.4X10-12 cu cm/molecule-sec at 25 °C(SRC) that was derived using a structure estimation method(3). n-Hexyl acetate does not contain chromophores that absorb at wavelengths >290 nm(4) and therefore is not expected to be susceptible to direct photolysis by sunlight(SRC).
Food Survey Values
n-Hexyl acetate was detected in apricots (4 ug/kg)(1), plums (2 ug/kg and 43 ug/kg)(1) and nectarines (10 ug/kg and 20 ug/kg)(2). n-Hexyl acetate was identified, not quantified, in apples(3,4), kiwi fruit(5) and beef volatiles(6). n-Hexyl acetate was detected in the head space samples of golden delicious apples after 24 hours incubation with pentanoic acid vapors and also in the essential oils(7).
Plant Concentrations
n-Hexyl acetate was reported in the skin and pulp of Queen Anne's pocket melon (Cucumis melo L) at 183 and 175.9 ug/kg equivalent of 2-octanol, respectively(1). n-Hexyl acetate was identified, not quantified, in the head space of intact golden delicious apples(2).
Soil Adsorption/Mobility
Using a structure estimation method based on molecular connectivity indices(1), the Koc of n-hexyl acetate can be estimated to be 62(SRC). According to a classification scheme(2), this estimated Koc value suggests that n-hexyl acetate is expected to have high mobility in soil.
Natural Pollution Sources
REPORTED FOUND IN FRUITAL AROMAS (EG FRAGARIA VESCA) & ESSENTIAL OILS.
n-Hexyl acetate occurs in many fruits(1-2) and may be released into the environment as a plant volatile(SRC).
Environmental Bioconcentration
An estimated BCF of 34 was calculated in fish for n-hexyl acetate(SRC), using an estimated log Kow of 2.83(1) and a regression-derived equation(2). According to a classification scheme(3), this BCF suggests the potential for bioconcentration in aquatic organisms is moderate(SRC).
Safety data
- PPE
- Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
- wgk
- 1
- tsca
- TSCA listed
- rtecs
- AI0875000
- ridadr
- UN 3272 3/PG 3
- hs_code
- 29153990
- Toxicity
- LD50 orally in Rabbit: 36100 mg/kg LD50 dermal Rabbit > 5000 mg/kg
- risk_code
- 10
- Signal word
- Warning
- Symbol(GHS)
- GHS02,GHS07
- safety_code
- 16
- hazard_class
- 3
- Storage Class
- 3 - Flammable liquids
- packing_group
- III
- Hazard statements
- H315+H320-H335-H226
- REACH Registrations
- Active
- Hazard Classifications
- Aquatic Chronic 2Flam. Liq. 3
- Precautionary statements
- P501-P240-P261-P210-P233-P243-P241-P242-P271-P264-P280-P370+P378-P337+P313-P305+P351+P338-P362+P364-P303+P361+P353-P332+P313-P304+P340+P312-P403+P233-P403+P235-P405
- Hazardous Substances Data
- 142-92-7(Hazardous Substances Data)
Chemistry & industry
Pharmacology
Uses & manufacturing
Uses
Used as a solvent for cellulose esters, cellulose, styrene, and phenolic resins; Also used as a spray base, flavoring agent, and fragrance for perfumes, soaps, detergents, and creams; [HSDB] Used as a propellant in aerosols; [CAMEO] Used as a leveling agent in paints; Occurs naturally in a number of fruits and alcoholic beverages; [CHEMINFO]
Painting (Pigments, Binders, and Biocides) [Category: Paint]
Solvent for cellulose esters and other resins; spray base.
It is present in a number of fruits and alcoholic beverages, and is used in fruit aroma compositions.
Leveling agent in paints
Reported uses (ppm):
U.S. Production
2023: 10,000,000 - <25,000,000 lb
(1981) PROBABLY GREATER THAN 2.27X10+6 GRAMS
(1982) PROBABLY GREATER THAN 2.27X10+6 GRAMS
Production volumes for non-confidential chemicals reported under the Inventory Update Rule. [Table#5478]
Production volume for non-confidential chemicals reported under the 2006 Inventory Update Rule. Chemical: Acetic acid, hexyl ester. Aggregated National Production Volume: 1 to < 10 million pounds.
Methods of Manufacturing
From n-hexyl alcohol and excess acetic anhydride at the boil or with an excess of acetic acid in the presence of concentrated sulfuric acid.
From primary and sec-hexyl alcohols
Use Classification
Fragrance Ingredients
Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes
Flavoring Agents -> JECFA Flavorings Index
General Manufacturing Information
Soap, Cleaning Compound, and Toilet Preparation Manufacturing
Acetic acid, hexyl ester: ACTIVE
Applications
DescriptionHexyl acetate has a pleasant fruity odor and bittersweet taste suggestive of pear. May be synthesized from n-hexyl alcohol and excess acetic anhydride at the boil or with an excess of acetic acid in the presence of concentrated sulfuric acid.
OccurrenceReported found in fruital aromas (e.g., Fragaria vesca) and essential oils. Also reported found in apple, apricot, banana, sweet cherry, citrus peel oils and juices, blueberry, black currants, guava, grapes, melon, peach, pear, raspberry, blackberry, strawberry, peas, sauerkraut, rye bread, cheeses, roasted beef, beer, rum, cognac, whiskies, cider, sherry, grape wines, coffee, tea, soybean, olive, passion fruit, beans, starfruit, mango, cauliflower, pear and apple brandy, quince, origanum, lovage leaf, corn oil, mangosteen (Garcia mangostana), Bourbon vanilla, clary sage, nectarine, naranjilla fruit, Chinese quince and chamomile oil.
Usesn-Hexyl acetate exhibits antimicrobial activity and can be used to improve the safety of minimally processed fruits. It is a fruity smelling fluid used as flavoring agent or in perfumes. It is a green leaf volatile from cabbage Brassica oleracea var. capitata L. It is used as plasticizers.
UsesHexyl acetate was used to study the activity of diamondback moth sex pheromone and larval frass volatiles, as well as green leaf volatiles from cabbage, on the natural enemies of the pest.
UsesHexyl Acetate is a flavouring agent due to its fruity odor and it is naturally present in many fruits and alcoholic beverages.
General DescriptionA colorless liquid with a mild sweet odor. Flash point 113°F. A moderate fire risk. Inhalation may cause adverse effects. Almost insoluble in water, soluble in alcohol and Propylene glycol, miscible with oils. When heated to high temperatures emits acrid smoke and fumes. Used as a solvent and as a propellant in aerosols.
Preparation methods
PreparationFrom n-hexyl alcohol and excess acetic anhydride at the boil or with an excess of acetic acid in the presence of concentrated sulfuric acid
Upstream & downstream products
Upstream raw materials
Downstream products
Suppliers28 total
Additional notes
DefinitionChEBI: The acetate ester of hexan-1-ol.
Related reactions
Linked notes
Loading…