isobutyl acrylate

acrylic acid, isobutyl ester

CAS: 106-63-8 C7 H12 O2 MW: 128.17104000

Identification

Nameisobutyl acrylate
IUPAC2-methylpropyl prop-2-enoate
CAS Number106-63-8
EINECS203-417-8
FDA UNIIU02509V73F
Molecular FormulaC7 H12 O2
Molecular Weight128.17104000
MDL NumberMFCD00042865
Nikkaji NumberJ33.774I
Beilstein1749388
XlogP32.20 (est)

Regulatory

DG SANTE Food Contact Materialsacrylic acid, isobutyl ester
FDA Mainterm (IAUFC)106-63-8 ; ISOBUTYL ACRYLATE

Physical Properties

Appearance colorless to pale yellow clear liquid (est)
Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Specific Gravity 0.89000 @ 20.00 °C.
Melting Point -61.00 °C. @ 760.00 mm Hg (est)
Boiling Point 138.00 °C. @ 760.00 mm Hg
Vapor Pressure 10.700000 mmHg @ 20.00 °C.
Vapor Density 4.4 ( Air = 1 )
Flash Point 86.00 °F. TCC ( 30.00 °C. )
logP (o/w) 2.220
Soluble in alcohol
Insoluble in water

No sensory data available

Safety Information

Preferred SDSView
Oral/Parenteral Toxicityoral-rat LD50 7070 ul/kg
Dermal Toxicityskin-rabbit LD50 891 ul/kg
Inhalation Toxicityinhalation-rat LC50 2000 National Technical Information Service. Vol. OTS0535072

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements', 'BEHAVIORAL: ALTERED SLEEP TIME (INCLUDING CHANGE IN RIGHTING REFLEX)\nLUNGS, THORAX, OR RESPIRATION: DYSPNEA']

Safety in Use

Categoryindirect food additives: adhesives and components of coatings
Recommendation for isobutyl acrylate usage levels up tonot for fragrance use.
Recommendation for isobutyl acrylate flavor usage levels up tonot for flavor use.

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Potential Uses

None Found

Natural Occurrence

not found in nature

Synonyms

acrylic acid isobutyl ester acrylic acid, isobutyl ester iso butyl 2-propenoate iso butyl propenoate iso butylacrylate 2- methyl propyl 2-propenoate 2- methylpropyl acrylate 2- methylpropyl prop-2-enoate 2- propenoic acid 2-methylpropyl ester propenoic acid isobutyl ester 2- propenoic acid isobutyl ester 2- propenoic acid, 2-methylpropyl ester propenoic acid, isobutyl ester PubMed: Efficient synthesis of Fmoc-protected phosphinic pseudodipeptides: Building blocks for the synthesis of matrix metalloproteinase inhibitors. PubMed: Trisannelation of acrylates to 1,3,5-benzenetricarboxylates by a Pd(OAc)2/HPMoV/CeCl3/O2 system. PubMed: Quantitative analysis of bucillamine in blood using high-performance liquid chromatography-mass spectrometry technique. PubMed: Gas chromatographic-mass spectrometric determination of tiopronin in human blood using acrylic acid esters as a derivatization reagent for the thiol group.