tert-butyl acetate
acetic acid, 1,1-dimethylethyl ester
 
Notes:
None found
  • Charkit Chemical
    • Charkit Chemical Corporation
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      about: Since 1982, Charkit has been committed to expanding the markets we serve as our roster of products and services continues to grow with us. Our substantial portfolio of personal care ingredients now include a wide array of luxury and exotic components to compliment the key products we have always offered. We have expanded our offerings to the nutraceutical, industrial, and resin markets with a growing roster of versatile and unique ingredients. We continue to lead the way in our traditional markets such as Metal and Water Treatment, Imaging, Flavor & Fragrance, Aroma and Food. Our Pharmaceutical offerings continue to expand, still anchored by the Boronic Derivatives that meet the demands of Suzuki coupling reactions. Please contact us to learn how we can help you reach your goals.
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      Product(s):
      BUTYL ACETATE, TERT-
       
  • Penta International
    • Penta International Corporation
      Chemistry innovation
      At Penta, our products and services help businesses do business better.
      For over 30 years, Penta Manufacturing Company has played a growing role in worldwide chemistry innovations and applications. As an industry leader, Penta continues to pioneer chemistry-based solutions for practically every area of commerce. Our products and expertise have helped fuel technical advances in dozens of commercial applications including flavoring, coloring, fragrances and chemical processes.
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      Product(s):
      02-48870 TERT-BUTYL ACETATE
       
  • TCI AMERICA
    • TCI AMERICA
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      Tokyo Chemical Industry Co., Ltd. (TCI) is a leading worldwide manufacturer of specialty organic chemicals founded in 1946. TCI provides organic laboratory chemicals as well as pharmaceutical, cosmetic and functional materials. More than 70 years of synthesis experience and multi-purpose plants enable TCI to offer more than 30,000 products as well as custom synthesis.
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      Product(s):
      A0026 tert-Butyl Acetate >99.0%(GC)
       
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CAS Number: 540-88-5Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 208-760-7
FDA UNII: 76N22HKP3X
Nikkaji Web: J4.030D
Beilstein Number: 1699506
MDL: MFCD00008807
XlogP3: 1.80 (est)
Molecular Weight: 116.16004000
Formula: C6 H12 O2
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome or firefox)
Category: solvents
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
Google Books: Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Google Patents: Search
US Patents: Search
EU Patents: Search
Pubchem Patents: Search
PubMed: Search
NCBI: Search
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Physical Properties:
Appearance: colorless to pale yellow clear liquid (est)
Assay: 98.00 to 100.00 % 
Food Chemicals Codex Listed: No
Melting Point: -62.00 °C. @ 760.00 mm Hg
Boiling Point: 97.00 °C. @ 760.00 mm Hg
Vapor Pressure: 47.000000 mmHg @ 25.00 °C.
Flash Point: 72.00 °F. TCC ( 22.22 °C. )
logP (o/w): 1.760
Soluble in:
 alcohol
 water, 8330 mg/L @ 25 °C (exp)
Insoluble in:
 water
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Organoleptic Properties:
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: solvents
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Suppliers:
Charkit Chemical
BUTYL ACETATE, TERT-
EMD Millipore
For experimental / research use only.
tert-Butyl Acetate
LyondellBasell Industries
tertiary-Butyl Acetate
Penta International
TERT-BUTYL ACETATE
Santa Cruz Biotechnology
For experimental / research use only.
tert-Butyl Acetate ≥99%
Shiva Chemicals and Pharmaceuticals
Tertiary Butyl Acetate
Sigma-Aldrich: Aldrich
For experimental / research use only.
tert-Butyl Acetate ≥99%
Silver Fern Chemical
tert-Butyl acetate
Odor: characteristic
Use: tert-Butyl Acetate is a colorless, flammable liquid with a camphor or blueberry-like odor. It in insoluble in water, but soluble in alcohol and ether.
TCI AMERICA
For experimental / research use only.
tert-Butyl Acetate >99.0%(GC)
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Safety Information:
Preferred SDS: View
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
oral-rat LD50  4100 mg/kg
BEHAVIORAL: ATAXIA BEHAVIORAL: ALTERED SLEEP TIME (INCLUDING CHANGE IN RIGHTING REFLEX) LUNGS, THORAX, OR RESPIRATION: DYSPNEA
National Technical Information Service. Vol. OTS0573684-1

Dermal Toxicity:
skin-rabbit LD50 > 2000 mg/kg
GASTROINTESTINAL: "HYPERMOTILITY, DIARRHEA" KIDNEY, URETER, AND BLADDER: OTHER CHANGES
National Technical Information Service. Vol. OTS0573684-1

Inhalation Toxicity:
inhalation-rat LC50 > 2230 mg/m3/4H
National Technical Information Service. Vol. OTS0573684-1

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Safety in Use Information:
Category: solvents
Recommendation for tert-butyl acetate usage levels up to:
 not for fragrance use.
 
Recommendation for tert-butyl acetate flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
NIOSH International Chemical Safety Cards: search
NIOSH Pocket Guide: search
Chemical Carcinogenesis Research Information System: Search
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 540-88-5
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 10908
National Institute of Allergy and Infectious Diseases: Data
WISER: UN 1123
WGK Germany: 1
 tert-butyl acetate
Chemidplus: 0000540885
EPA/NOAA CAMEO: hazardous materials
RTECS: 540-88-5
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References:
 tert-butyl acetate
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 540-88-5
Pubchem (cid): 10908
Pubchem (sid): 134975744
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Other Information:
(IUPAC): Atomic Weights of the Elements 2011 (pdf)
Videos: The Periodic Table of Videos
tgsc: Atomic Weights use for this web site
(IUPAC): Periodic Table of the Elements
CHEMBL: View
HMDB (The Human Metabolome Database): Search
Export Tariff Code: 2915.39.9000
ChemSpider: View
Wikipedia: View
Formulations/Preparations:
texaco lead appreciator
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Potential Blenders and core components note
 
None Found
 
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Potential Uses:
None Found
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Occurrence (nature, food, other): note
 not found in nature
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Synonyms:
 acetic acid 1,1-dimethylethyl ester
 acetic acid t-butyl ester
 acetic acid tert-butyl ester
 acetic acid, 1,1-dimethylethyl ester
 acetic acid, tert-butyl ester
T-butyl acetate
tert-butyl ester of acetic acid
tert-butyl ethanoate
tert-butylacetate
1,1-dimethyl acetate
1,1-dimethylethyl acetate
2-methyl-2-propanyl acetate
 texaco lead appreciator
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Articles:
PubMed: Solvent-tolerance of fungi located on an interface between an agar plate and an organic solvent.
PubMed: Evaluation of the cross section of elongated micelles by static and dynamic light scattering.
PubMed: Bell-shaped extraction device assisted liquid-liquid microextraction technique and its optimization using response-surface methodology.
PubMed: Comparative analysis of tertiary alcohol esterase activity in bacterial strains isolated from enrichment cultures and from screening strain libraries.
PubMed: General method for selective labelling of double-chain cysteine-rich peptides with a lanthanide chelate via solid-phase synthesis.
PubMed: LC50 Determination of tert-Butyl Acetate using a Nose Only Inhalation Exposure in Rats.
PubMed: Nucleophilic addition to 2,3-disubstituted butanal derivatives and their application to natural product synthesis.
PubMed: Iridium-catalyzed alpha-alkylation of acetates with primary alcohols and diols.
PubMed: [H2O2 oxidation of 1,4-dihydropyridines over Mg2+ ion exchanged clinoptilolite and solventless solid state acid decomposition of ester to 3,5-pyridinedicarboxylic acid].
PubMed: An efficient and scalable Ritter reaction for the synthesis of tert-butyl amides.
PubMed: Oxidation in three-liquid-phase microemulsion systems using "Balanced Catalytic Surfactants".
PubMed: Amphiphilic hyperbranched fluoropolymers as nanoscopic 19F magnetic resonance imaging agent assemblies.
PubMed: Palladium-catalyzed alpha-arylation of esters with chloroarenes.
PubMed: Effects of tert-butyl acetate on maternal toxicity and embryo-fetal development in Sprague-Dawley rats.
PubMed: Asymmetric synthesis of orthogonally protected trans-cyclopropane gamma-amino acids via intramolecular ring closure.
PubMed: Synthesis of 2H-1,2-benzothiazine 1,1-dioxides via heteroannulation reactions of 2-iodobenzenesulfonamide with ketone enolates under S(RN)1 conditions.
PubMed: Palladium-catalyzed alpha-arylation of esters and amides under more neutral conditions.
PubMed: Synthesis of jenamidines A1/A2.
PubMed: Interfacial reactions in confinement: kinetics and temperature dependence of the surface hydrolysis of polystyrene-block-poly(tert-butyl acrylate) thin films.
PubMed: The mutagenicity testing of tertiary-butyl alcohol, tertiary-butyl acetate and methyl tertiary-butyl ether in Salmonella typhimurium.
PubMed: Acute toxicity and cancer risk assessment values for tert-butyl acetate.
PubMed: Development of new synthetic methods with aryl 1-chlorovinyl sulfoxides.
PubMed: Fluorogenic stereochemical probes for transaldolases.
PubMed: Efficient synthesis of alpha-aryl esters by room-temperature palladium-catalyzed coupling of aryl halides with ester enolates.
PubMed: Polymorphic behavior of an NK1 receptor antagonist.
PubMed: Extremely stable and versatile carboxylesterase from a hyperthermophilic archaeon.
PubMed: Tailoring fatty food simulants made from solvent mixtures (2): determining the equivalent migration behaviour of olive oil and of solvents in the case of polyolefins.
PubMed: Antimicrobial and bactericidal activities of esters of 2-endo-hydroxy-1,8-cineole as new aroma chemicals.
PubMed: Tailoring fatty food simulants made from solvent mixtures (1): comparison of methanol, ethanol and isopropanol behaviour with polystyrene.
PubMed: Syntheses of stereochemically restricted lactone-type analogues of jasmonic acids.
PubMed: Application of tryptamine as a derivatizing agent for the determination of airborne isocyanates. Part 7. Selection of impinger solvents and the evaluation against dimethyl sulfoxide used in US NIOSH Regulatory Method 5522.
PubMed: Food and packaging interactions: tailoring fatty food simulants.
PubMed: Inhaled tert-butyl acetate and its metabolite tert-butyl alcohol accumulate in the blood during exposure.
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