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Butyl acetate

CAS No.
123-86-4
Chemical Name:
Butyl acetate
Synonyms
N-BUTYL ACETATE;ACETIC ACID BUTYL ESTER;Acetic acid butyl;Butylacetat;Butyl ethanoate;Butyle;butylacetates;Butile;BUTYLE ACETATE;1-Butyl acetate
CBNumber:
CB6671615
Molecular Formula:
C6H12O2
Lewis structure
c6h12o2 lewis structure
Molecular Weight:
116.16
MDL Number:
MFCD00009445
MOL File:
123-86-4.mol
MSDS File:
SDS
Last updated:2024-10-24 21:11:45

Butyl acetate Properties

Melting point -78 °C (lit.)
Boiling point 124-126 °C (lit.)
Density 0.88 g/mL at 25 °C (lit.)
vapor density 4 (vs air)
vapor pressure 15 mm Hg ( 25 °C)
refractive index n20/D 1.394(lit.)
FEMA 2174 | BUTYL ACETATE
Flash point 74 °F
storage temp. Store at +5°C to +30°C.
solubility 5.3g/l
form Liquid
Specific Gravity 0.883 (20/20℃)
color ≤10(APHA)
Odor Characteristic; agreeable fruity (in low concentrations); non residual.
PH 6.2 (5.3g/l, H2O, 20℃)(External MSDS)
explosive limit 1.4-7.5%(V)
Odor Threshold 0.016ppm
Odor Type ethereal
Viscosity 0.83mm2/s
Water Solubility 0.7 g/100 mL (20 ºC)
FreezingPoint -77.9℃
λmax λ: 254 nm Amax: 1.0
λ: 260 nm Amax: 0.20
λ: 275 nm Amax: 0.04
λ: 300 nm Amax: 0.02
λ: 320-400 nm Amax: 0.01
Merck 14,1535
JECFA Number 127
BRN 1741921
Henry's Law Constant 5.79 at 37 °C (static headspace-GC, van Ruth et al., 2001)
Dielectric constant 5.0(20℃)
Exposure limits TLV-TWA 150 ppm (~710 mg/m3) (ACGIH, MSHA, and OSHA); TLV-STEL 200 ppm (~950 mg/m3); IDLH 10,000 ppm (NIOSH).
Stability Stable. Flammable. Incompatible with strong oxidizing agents, strong acids, strong bases.
InChIKey DKPFZGUDAPQIHT-UHFFFAOYSA-N
LogP 1.82-2.3 at 25℃
Substances Added to Food (formerly EAFUS) BUTYL ACETATE
FDA 21 CFR 172.515; 175.105; 175.320; 177.1200
CAS DataBase Reference 123-86-4(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII 464P5N1905
NIST Chemistry Reference Acetic acid, butyl ester(123-86-4)
EPA Substance Registry System n-Butyl acetate (123-86-4)
Cosmetics Info Butyl Acetate

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS02,GHS07
Signal word  Warning
Hazard statements  H226-H336
Precautionary statements  P210
Risk Statements  10-66-67-R67-R66-R10
Safety Statements  25-S25
RIDADR  UN 1123 3/PG 3
OEB A
OEL TWA: 150 ppm (710 mg/m3), STEL: 200 ppm (950 mg/m3)
WGK Germany  1
RTECS  AF7350000
Autoignition Temperature 790 °F
TSCA  Yes
HS Code  2915 33 00
HazardClass  3
PackingGroup  III
Toxicity LD50 orally in rats: 14.13 g/kg (Smyth)
IDLA 1,700 ppm
NFPA 704
3
2 0

Butyl acetate price More Price(56)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich W217417 Butyl Acetate natural, ≥98%, FG 123-86-4 100g $76 2024-03-01 Buy
Sigma-Aldrich W217417 Butyl Acetate natural, ≥98%, FG 123-86-4 1kg $128 2024-03-01 Buy
Sigma-Aldrich W217417 Butyl Acetate natural, ≥98%, FG 123-86-4 4kg $383 2024-03-01 Buy
Sigma-Aldrich W217409 Butyl Acetate ≥99%, FCC, FG 123-86-4 1kg $77.5 2024-03-01 Buy
Sigma-Aldrich W217409 Butyl Acetate ≥99%, FCC, FG 123-86-4 9kg $308 2024-03-01 Buy
Product number Packaging Price Buy
W217417 100g $76 Buy
W217417 1kg $128 Buy
W217417 4kg $383 Buy
W217409 1kg $77.5 Buy
W217409 9kg $308 Buy

Butyl acetate Chemical Properties,Uses,Production

Description

Butyl acetate is a clear, flammable ester of acetic acid that occurs in n-, sec-, and tert- forms (INCHEM, 2005). Butyl acetate isomers have a fruity, banana-like odor (Furia, 1980). Isomers of butyl acetate are found in apples (Nicholas, 1973) and other fruits (Bisesi, 1994), as a well as in a number of food products, such as cheese, coffee, beer, roasted nuts, vinegar (Maarse and Visscher, 1989). Butyl acetate is manufactured via esterification of the respective alcohol with acetic acid or acetic anhydride (Bisesi, 1994). N-butyl acetate is used as a solvent for nitrocellulose-based lacquers, inks, and adhesives. Other uses include manufacture of artificial leathers, photographic film, safety glass, and plastics (Budavari, 1996). Isomers of butyl acetate are also used as flavoring agents, in manicure products, and as larvicides (Bisesi, 1994). The tert-isomer has been used as a gasoline additive (Budavari, 1996). It may be used as a synthetic fruit flavoring in candy, ice cream, cheeses, and baked goods (Dikshith, 2013).
Butyl acetate

Chemical Properties

Butyl acetate is a colorless or yellowish liquid with a strong fruity odor. burning and then sweet taste reminiscent of pineapple. It occurs in many fruits and is a constituent of apple aromas. Butyl acetate is incompatible with strong oxidizing agents, strong acids, and strong bases.
There are 4 isomers. At 20 °C, the density of the n-butyl isomer is 0.8825 g/ cm3, and the density of the sec-isomer is 0.8758 g/cm3 (Bisesi, 1994). The n-butyl isomer is soluble in most hydrocarbons and acetone, and it is miscible with ethanol, ethyl ether, and chloroform (Haynes, 2010). It dissolves many plastics and resins (NIOSH, 1981).

Physical properties

Clear, colorless liquid with a strong fruity odor resembling bananas. Sweetish taste as low concentrations (<30 μg/L). Experimentally determined detection and recognition odor threshold concentrations were 30 μg/m3 (6.3 ppbv) and 18 μg/m3 (38 ppbv), respectively (Hellman and Small, 1974). Cometto-Mu?iz et al. (2000) reported nasal pungency threshold concentrations ranged from approximately 550 to 3,500 ppm.

Occurrence

Reported present in rum ether, pears, pear brandy, cider, mango, mountain papaya (C. pubescens), soybean, roasted peanuts and honey and other natural products.

Uses

Butyl acetate is one of the more important derivatives of n-butyl alcohol produced commercially, is employed as a solvent in rapid drying paints and coatings. In some instances, butyl acetate, C6H12O2, has replaced ethoxyethyl acetate due to the latter’s reported toxicity and teratogenicity.

Uses

n-Butyl acetate is used in the manufactureof lacquers, plastics, photographic films, andartificial leathers.

Uses

Butyl Acetate is a flavoring agent which is a clear, colorless liquid possessing a fruity and strong odor. it is sparingly soluble in water and miscible in alcohol, ether, and propylene glycol. it is also termed n-butyl acetate.

Definition

ChEBI: Butyl acetate is the acetate ester of butanol. It has a role as a metabolite. It is functionally related to a butan-1-ol.

Production Methods

Butyl alcohol is combined with acetic acid in the presence of a catalyst such as sulfuric acid. After esterification is complete, the solution is distilled to yield butyl acetate .

Preparation

By esterification of n-butyl alcohol with acetic acid.

Aroma threshold values

Detection: 10 to 500 ppb

Synthesis Reference(s)

Journal of the American Chemical Society, 73, p. 5265, 1951 DOI: 10.1021/ja01155a075
The Journal of Organic Chemistry, 39, p. 3728, 1974 DOI: 10.1021/jo00939a026

General Description

A clear colorless liquid with a fruity odor. Flash point 72 - 88°F. Density 7.4 lb / gal (less than water). Hence floats on water. Vapors heavier than air.

Air & Water Reactions

Highly flammable. Very slightly soluble in water.

Reactivity Profile

Butyl 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. Attacks many plastics. [Handling Chemicals Safely 1980. p. 233].

Hazard

Skin irritant, toxic. Flammable, moderate fire risk. Eye and upper respiratory tract irritant.

Health Hazard

The narcotic effects of n-butyl acetate isgreater than the lower alkyl esters of aceticacid. Also, the toxicities and irritant actionsare somewhat greater than n-propyl, iso propyl, and ethyl acetates. Exposure to its vapors at about 2000 ppm caused mild irritation of the eyes and salivation in test animals. A 4-hour exposure to 14,000 ppm wasfatal to guinea pigs. In humans, inhalation of 300-400 ppm of n-butyl acetate may produce moderate irritation of the eyes and throat, and headache.

Health Hazard

Exposures to n-butyl acetate cause harmful effects that include, but are not limited to, coughing and shortness of breath. High concentrations have a narcotic effect, with symp toms such as sore throat, abdominal pain, nausea, vomiting, and diarrhea. High concen trations of n-butyl acetate cause severe poisoning. Prolonged periods of exposure cause adverse effects to the lungs, the nervous system, and the mucous membranes. Repeated skin contact causes skin dryness or cracking, and dermatitis.

Fire Hazard

HIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames. Vapors may form explosive mixtures with air. Vapors may travel to source of ignition and flash back. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapor explosion hazard indoors, outdoors or in sewers. Runoff to sewer may create fire or explosion hazard. Containers may explode when heated. Many liquids are lighter than water.

Biochem/physiol Actions

Taste at 30 ppm

Safety Profile

Moderately toxic by intraperitoneal route. Mdly toxic by inhalation and ingestion. An experimental teratogen. A skin and severe eye irritant. Human systemic effects by inhalation: conjunctiva irritation, unspecified nasal and respiratory system effects. A mild allergen. High concentrations are irritating to eyes and respiratory tract and cause narcosis. Evidence of chronic systemic toxicity is inconclusive. Flammable liquid. Moderately explosive when exposed to flame. Ignites on contact with potassium tert-butoxide. To fight fire, use alcohol foam, CO2, dry chemical. When heated to decomposition it emits acrid and irritating fumes. See also ESTERS.

Potential Exposure

n-Butyl acetate is an important solvent in the production of lacquers, leather and airplane dopes, and perfumes. It is used as a solvent and gasoline additive. sec-Butyl acetate is used as a widely used solvent for nitrocellulose, nail enamels and many different purposes. tert-Butyl acetate is common industrial solvent used in the making of lacquers, artificial leather, airplane dope, perfume; and as a food additive. Isobutyl acetate is used as a solvent and in perfumes and artificial flavoring materials

First aid

If this chemical gets into the eyes, remove anycontact lenses at once and irrigate immediately for at least15 min, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts theskin, remove contaminated clothing and wash immediatelywith soap and water. Seek medical attention immediately. Ifthis chemical has been inhaled, remove from exposure,begin rescue breathing (using universal precautions, including resuscitation mask) if breathing has stopped and CPR ifheart action has stopped. Transfer promptly to a medicalfacility. When this chemical has been swallowed, get medical attention. Give large quantities of saltwater and inducevomiting. Do not make an unconscious person vomit.

Carcinogenicity

There are no indications of mutagenic or cytogenic effects for n-butyl acetate.

Source

Identified as a volatile constituent released by fresh coffee beans (Coffea canephora variety Robusta) at different stages of ripeness (Mathieu et al., 1998). Also identified among 139 volatile compounds identified in cantaloupe (Cucumis melo var. reticulates cv. Sol Real) using an automated rapid headspace solid phase microextraction method (Beaulieu and Grimm, 2001).

storage

n-Butyl acetate should be kept stored in a segregated and approved area. Workers should keep the container in a cool, well-ventilated area, closed tightly, and sealed until ready for use. Workers should avoid all possible sources of ignition/spark at the workplace

Shipping

UN1123 Butyl acetates, Hazard Class: 3; Labels: 3—Flammable liquid.

Purification Methods

Distil, reflux with successive small portions of KMnO4 until the colour persists, dry with anhydrous CaSO4, filter and redistil. [Beilstein 2 IV 143.]

Incompatibilities

All butyl acetates are incompatible with nitrates, strong oxidizers; strong alkalies; strong acids. Butyl acetates may form explosive mixture with air; reacts with water, on standing, to form acetic acid and n-butyl alcohol. Violent reaction with strong oxidizers and potassium-tert-butoxide. Dissolves rubber, many plastics, resins and some coatings. May accumulate static electrical charges, and may cause ignition of its vapors

Waste Disposal

Dissolve or mix the material with a combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber. All federal, state, and local environmental regulations must be observed.

Precautions

On exposure to Butyl acetate, immediately wash with plenty of water, also under the eyelids, for at least 15 min. Remove contact lenses. Butyl acetate is flammable in the pres ence of open flames, sparks, oxidizing materials, acids, and alkalis. It poses explosion risk in the presence of mechanical impact. For health safety, management authorities should provide exhaust ventilation facilities at the workplace to keep the airborne concentrations of vapors of Butyl acetate below TLV.

108-24-7
71-36-3
123-86-4
Synthesis of Butyl acetate from Acetic anhydride and 1-Butanol
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View Lastest Price from Butyl acetate manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Butyl acetate pictures 2024-11-28 Butyl acetate
123-86-4
US $0.00 / KG 1KG 99% 1000mt/year Jinan Finer Chemical Co., Ltd
Butyl acetate pictures 2024-11-14 Butyl acetate
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US $160.00 / KG 1KG 98% 1-20mt Baoji Guokang Bio-Technology Co., Ltd.
Butyl acetate pictures 2024-10-29 Butyl acetate
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US $0.00 / kg 20kg 99.0% 20 tons Qingdao RENAS Polymer Material Co., Ltd.
  • Butyl acetate pictures
  • Butyl acetate
    123-86-4
  • US $0.00 / KG
  • 99%
  • Jinan Finer Chemical Co., Ltd
  • Butyl acetate pictures
  • Butyl acetate
    123-86-4
  • US $160.00 / KG
  • 98%
  • Baoji Guokang Bio-Technology Co., Ltd.
  • Butyl acetate pictures
  • Butyl acetate
    123-86-4
  • US $0.00 / kg
  • 99.0%
  • Qingdao RENAS Polymer Material Co., Ltd.
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