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06958

Supelco

Butyl acrylate

analytical standard

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About This Item

Linear Formula:
CH2=CHCOO(CH2)3CH3
CAS Number:
141-32-2
Molecular Weight:
128.17
Beilstein:
1749970
EC Number:
205-480-7
MDL number:
MFCD00009446
UNSPSC Code:
41116107
PubChem Substance ID:
329748313
NACRES:
NA.24
Pricing and availability is not currently available.

grade

analytical standard

Quality Level

100

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
GHS02,GHS07

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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Certificates of Analysis (COA)

Lot/Batch Number
BCCL5319
BCCJ3969
BCCF1959
BCCC6200
BCCC1025

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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
Jérôme Garnier et al.
Macromolecular rapid communications, 33(16), 1388-1392 (2012-05-19)
Hybrid latexes based on cerium oxide nanoparticles are synthesized via an emulsifier-free process of emulsion polymerization employing amphiphatic macro-RAFT agents. Poly(butyl acrylate-co-acrylic acid) random oligomers of various compositions and chain lengths are first obtained by RAFT copolymerization in the presence
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
Ci Song et al.
Carbohydrate polymers, 91(1), 217-223 (2012-10-10)
This article reports the preparation and evaluation of polymeric microspheres as a new class of oil-absorbent (POAMs). Based on our earlier oil-absorbents, the present microspheres contained β-cyclodextrin (β-CD) moieties as both cross-linking agent and porogen agent, and showed exciting high
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
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