tert-Butyl acetate

HCID 10908CAS 540-88-5

Basic information

Standard SMILES
CC(=O)OC(C)(C)C
InChIKey
WMOVHXAZOJBABW-UHFFFAOYSA-N
Molecular formula
C6H12O2
Average molar mass
116.16 g/mol
Monoisotopic mass
116.08372962

Overview

Tert-butyl acetate is a colorless liquid with a mild odor. Floats on water. Produces irritating vapor. (USCG, 1999)

Names & identifiers

Preferred name
tert-Butyl acetate
IUPAC
tert-butyl acetate
English name
tert-Butyl acetate
Molecular formula
C6H12O2
Molecular weight
116.16

Names & synonyms

TERT-BUTYL ACETATE540-88-5t-Butyl acetateAcetic acid, 1,1-dimethylethyl esterTexaco lead appreciatorAcetic acid, tert-butyl ester1,1-Dimethyl acetateDTXSID102205576N22HKP3XNSC-59719DTXCID702055tert-Butyl ester of acetic acid
Show more names
TLATert-buty acetatetertiairybutylacetateTILACTBAC(TM)tertiairyAcetic acid-teCH3C(O)OC(CH3)3
RefChem:188195208-760-7tert-Butyl ethanoateAcetic Acid tert-Butyl Estertert-butylacetatetert butyl acetate1,1-dimethylethyl acetateNSC 59719

Database identifiers

CAS
540-88-5
PubChem CID
10908
DTXSID
DTXSID1022055
ChEMBL
CHEMBL3186747
UNII
76N22HKP3X
EC Number
208-760-7
Nikkaji
J3.290E

Properties

Computed structural properties

XLogP
1.8
Topological polar surface area
26.3 Ų
Hydrogen bond donors
0
Hydrogen bond acceptors
2
Rotatable bonds
2
Heavy atoms
8

Experimental & physicochemical properties

Chemical ClassesFlammable agents - 3rd degree
SolventsSolvents -> Esters (<C12)
CosmeticsCosmetic ingredients (t-Butyl Acetate) -> CIR (Cosmetic Ingredient Review)
SpringerMaterials PropertiesSchoenflies notation
LogP · 3 items

log Kow = 1.76

1.76

1.76

OdorFruity odor

Physicochemical properties

Melting point
-62 °C · -62°C
Boiling point
98 °C · 98 °C
Density
0.866 g/mL · 0.866 g/mL at 20 °C(lit.)
vapor density
4.01 · 4.01 (vs air)
vapor pressure
41 hPa · 41 hPa (20 °C)
refractive index
20 · n20/D 1.386(lit.)

Safety & regulation

GHS classification

GHS Classification · 6 items

Danger

H225: Highly Flammable liquid and vapor [Danger Flammable liquids]

P210, P233, P240, P241, P242, P243, P280, P303+P361+P353, P370+P378, P403+P235, and P501 (click each P-code to see the statement)

This chemical does not meet GHS hazard criteria for < 0.1% (1 of 1382) of reports.

Danger

H225 (> 99.9%): Highly Flammable liquid and vapor [Danger Flammable liquids]

Hazard information

Regulatory Information · 6 items

Chemical: Acetic acid, 1,1-dimethylethyl ester

Regulation (EC) No 178/2002 (amended)

Acetic acid, 1,1-dimethylethyl ester is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Acetic acid, 1,1-dimethylethyl 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: 05-10-2021 https://echa.europa.eu/registration-dossier/-/registered-dossier/10192

Acetic acid, 1,1-dimethylethyl ester: HSNO Approval: HSR001094 Approved with controls

The New Jersey Worker and Community Right to Know Act requires public and private employers to provide information about hazardous substances at their workplaces. (N.J.S.A. 34:5A-1 et. seq.)

Other Safety InformationIMAP assessments - Acetate esters (C2-C4): Human health tier II assessment
DOT LabelFlammable Liquid
Fire Hazards · 2 items

Excerpt from ERG Guide 129 [Flammable Liquids (Water-Miscible / Noxious)]:

Highly flammable. Above 15.5 °C explosive vapour/air mixtures may be formed.

Fire PotentialFlammable.
Health HazardsINHALATION: Irritation of throat. EYES: Irritation. (USCG, 1999)

Safety & protection

Fire Fighting · 2 items

Fire Extinguishing Agents Not to Be Used: Water may be ineffective.

Use carbon dioxide, dry powder, foam. In case of fire: keep drums, etc., cool by spraying with water.

First Aid Measures · 4 items

Fresh air, rest.

Remove contaminated clothes. Rinse and then wash skin with water and soap.

First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.

Rinse mouth.

First Aid · 2 items

Excerpt from NIOSH Pocket Guide for tert-Butyl acetate:

(General first aid procedures)

Safe StorageFireproof. Separated from strong oxidants, strong bases and strong acids.
Exposure Control and Personal Protection20.0 [ppm]
Fire Fighting ProceduresTo fight fire, use alcohol foam, CO2, dry chemical.

Toxicology

Target Organsrespiratory system, eyes, skin, central nervous system
Ecotoxicity Values · 3 items

EC50; Species: Chlorococcales (Green Algae Order); Conditions: freshwater, static; Concentration: 1300000 ug/L for 24 hr; Effect: physiology, assimilation efficiency /formulation/

LC50; Species: Daphnia magna (Water Flea) age < or =24 hr; Conditions: freshwater, static, 20-22 °C; Concentration: 4730000 ug/L for 24 hr /formulation/

LC50; Species: Pimephales promelas (Fathead minnow) age 30 days, length 20.8 mm, weight 0.136 g; Conditions: freshwater, flow through, 25 °C, pH 7.5, hardness 44.8 mg/L CaCO3, alkalinity 43.3 mg/L CaCO3, dissolved oxygen 6.7 mg/L; Concentration: 327000 ug/L for 96 hr (95% confidence interval: 296000-362000 ug/L) /99+% purity/

Environmental Fate · 3 items

TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 12(SRC), determined from a structure estimation method(2), indicates that tert-butyl acetate is expected to have very high mobility in soil(SRC). Volatilization of tert-butyl acetate from moist soil surfaces is expected to be an important fate process(SRC) given an estimated Henry's Law constant of 4.1X10-4 atm-cu m/mole(SRC), using a fragment constant estimation method(3). tert-Butyl acetate is expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 47 mm Hg at 25 °C(4). No biodegradation studies have been located for tert-butyl acetate, however, studies on structurally similar compounds(5-7) have shown that, in general, the ester functional group of alkyl acetates are biodegradable(SRC).

AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 12(SRC), determined from a structure estimation method(2), indicates that tert-butyl acetate is not expected to adsorb to suspended solids and sediment(SRC). Volatilization from water surfaces is expected(3) based upon an estimated Henry's Law constant of 4.1X10-4 atm-cu m/mole(SRC), developed using a fragment constant estimation method(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 days, respectively(SRC). According to a classification scheme(5), an estimated BCF of 7(SRC), from its log Kow of 1.76(6) and a regression-derived equation(7), suggests the potential for bioconcentration in aquatic organisms is low(SRC). No biodegradation studies have been located for tert-butyl acetate, however, studies on structurally similar compounds(8-10) have shown that, in general, the ester functional group of alkyl acetates are biodegradable(SRC). Hydrolysis is expected to occur slowly based upon experimentally determined hydrolysis half-lives of 135, 14.6 and 1.5 years at pH 7, 8 and 9, respectively(11).

ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), tert-butyl acetate, which has a vapor pressure of 47 mm Hg at 25 °C(2), is expected to exist solely as a vapor in the ambient atmosphere. Vapor-phase tert-butyl 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 36 days(SRC), calculated from its rate constant of 4.5X10-13 cu cm/molecule-sec at 25 °C(3). tert-Butyl 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 Valuestert-Butyl acetate occurs naturally in bananas and other related fruits(1).
Adverse EffectsNeurotoxin - Acute solvent syndrome
Exposure Routes · 2 items

The substance can be absorbed into the body by inhalation of its vapour.

inhalation, ingestion, skin and/or eye contact

Regulatory information

TSCA Requirements · 2 items

Section 8(a) of TSCA requires manufacturers of this chemical substance to report preliminary assessment information concerned with production, exposure, and use to EPA as cited in the preamble in 51 FR 41329. Effective date 1/26/94; Reporting date: 3/28/94.

Pursuant to section 8(d) of TSCA, EPA promulgated a model Health and Safety Data Reporting Rule. The section 8(d) model rule requires manufacturers, importers, and processors of listed chemical substances and mixtures to submit to EPA copies and lists of unpublished health and safety studies. tert-Butyl acetate is included on this list. Effective date: 1/26/94; Sunset date: 6/30/98.

CERCLA Reportable Quantities · 1 item

Persons in charge of vessels or facilities are required to notify the National Response Center (NRC) immediately, when there is a release of this designated hazardous substance, in an amount equal to or greater than its reportable quantity of 5000 lb or 2270 kg. The toll free number of the NRC is (800) 424-8802. The rule for determining when notification is required is stated in 40 CFR 302.4 (section IV. D.3.b).

Clean Water Act Requirements · 1 item

tert-Butyl acetate is designated as a hazardous substance under section 311(b)(2)(A) of the Federal Water Pollution Control Act and further regulated by the Clean Water Act Amendments of 1977 and 1978. These regulations apply to discharges of this substance. This designation includes any isomers and hydrates, as well as any solutions and mixtures containing this substance.

Safety data

OEB
A
OEL
TWA: 200 ppm (950 mg/m3)
PPE
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
wgk
1
IDLA
1,500 ppm
tsca
TSCA listed

Chemistry & industry

Pharmacology

Mechanism of Action... /tert-Butyl acetate/ behaved as inhibitor of acetylcholine when it combined with the acetylcholine receptor on the muscle.
Biological Half-Life... When tert-butyl acetate was added to human blood samples the... /half-life/ was 300 minutes.
Metabolism/Metabolites · 2 items

Butyl acetates are readily hydrolyzed to acid and alcohol in blood, liver, small intestines and respiratory passages, and this has been demonstrated in vitro in homogenates. ... /butyl acetates/

A continuous 5 hr-exposure to approximately 440 ppm tert-butyl acetate in air (via a tracheal canule) resulted in continuously increasing concentrations of tert-butyl acetate and tert-butyl alcohol (metabolite of tert-butyl acetate) in the blood of rats. This accumulation of tert-butyl acetate and tert-butyl alcohol was reproduced during a continuous exposure to about 900 ppm tert-butyl acetate in air over a period of 4 hr and 15 min. After the inhalation approximately 50% of the blood level of tert-butyl acetate decreased within 45 min, but that of tert-butyl alcohol remained unchanged at a high level.

Uses & manufacturing

Uses · 5 items

CIR ingredient: t-Butyl Acetate

Used as a solvent (industrial coatings, inks, adhesives, cleaners) and gasoline additive; Bananas and other fruits are food sources. [ACGIH]

Painting (Solvents) [Category: Paint]

Solvent, gasoline additive

Antiknock action enhancer of tetraethyl lead, especially at very high octane levels.

U.S. Production · 3 items

2023: 10,000,000 - <25,000,000 lb

Production volumes for non-confidential chemicals reported under the Inventory Update Rule. [Table#2260]

Production volume for non-confidential chemicals reported under the 2006 Inventory Update Rule. Chemical: Acetic acid, 1,1-dimethylethyl ester. Aggregated National Production Volume: 1 to < 10 million pounds.

Consumer UsesSolvent
Industry UsesFuel agents
Methods of ManufacturingPrepared from isobutylene reacting with acetic acid in the liquid phase with vanadium pentoxide impregnated silica as catalyst and with heat to increase the yield.
Formulations/PreparationsTEXACO LEAD APPRECIATOR

Applications

Usestert-Butyl acetate is common industrial solvent used in the making of lacquers, artificial leather, airplane dope, perfume, and as a food additive. It has recently gained EPA volatile organic compound (VOC) exempt status.

Related reactions

558 records

Linked notes

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