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Key Documents

06958

Supelco

Butyl acrylate

analytical standard

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About This Item

Linear Formula:
CH2=CHCOO(CH2)3CH3
CAS Number:
Molecular Weight:
128.17
Beilstein:
1749970
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

vapor density

>1 (vs air)

vapor pressure

3.3 mmHg ( 20 °C)

Assay

≥99.5% (GC)

autoignition temp.

559 °F

shelf life

limited shelf life, expiry date on the label

contains

~0.0015% hydroquinone monomethyl ether as stabilizer

expl. lim.

9.9 %

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.418 (lit.)
n20/D 1.419

bp

145 °C (lit.)

density

0.899 g/mL at 20 °C
0.894 g/mL at 25 °C (lit.)

application(s)

environmental

format

neat

SMILES string

CCCCOC(=O)C=C

InChI

1S/C7H12O2/c1-3-5-6-9-7(8)4-2/h4H,2-3,5-6H2,1H3

InChI key

CQEYYJKEWSMYFG-UHFFFAOYSA-N

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General description

This substance is listed on the positive list of the EU regulation 10/2011 for plastics intended to come into contact with food.

Pictograms

FlameExclamation mark

Signal Word

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Aquatic Chronic 3 - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

100.4 °F - closed cup

Flash Point(C)

38 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Li Wang et al.
Organic letters, 13(23), 6137-6139 (2011-11-08)
Pd(II)-catalyzed aromatic C-H bond activation using urea as a directing group was achieved in a p-TsOH/AcOH medium under mild reaction conditions. The direct olefination products of various urea derivatives were produced from aryl urea derivatives and butyl acrylate in moderate
M Obiols-Rabasa et al.
Langmuir : the ACS journal of surfaces and colloids, 26(11), 7717-7724 (2010-02-04)
The seeded semicontinuous emulsion copolymerization of methyl methacrylate (MMA) and butyl acrylate (BuA) stabilized with a graft polymeric surfactant based on inulin, INUTEC SP1, as well as its mixture with sodium lauryl sulfate (SLS) is described. The mixture of SLS
Jianqi Zhang et al.
Langmuir : the ACS journal of surfaces and colloids, 27(19), 12197-12200 (2011-08-31)
The influence of solvent annealing on microscopic deformational behavior of a styrene/n-butyl acrylate copolymer latex film subjected to uniaxial tensile deformation was studied by small-angle X-ray scattering. It was demonstrated that the microscopic deformation mechanism of the latex films transformed
Shuzhao Li et al.
Biomacromolecules, 12(9), 3305-3312 (2011-07-30)
Immobilizing poly(butyl acrylate) (PBA) on cellulose microfibrils (CMFs) by atom transfer radical polymerization (ATRP) of butyl acrylate (BA) on the surface of 2-bromoisobutyryl-functionalized CMF generated highly hydrophobic microfibrils (CMF-PBA) with a hard core and a soft-shell structure. TGA and static
Paula C Pinheiro et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 101, 36-39 (2012-10-25)
Enhancement of Raman signals of the nucleobase adenine on an Ag based composite was studied using the 1064 nm laser line. The composite comprise emulsions of Ag nanoparticles encapsulated in poly(t-butylacrylate) (PtBA) beads that act as substrate for the Surface-Enhanced

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