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Merck

06958

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
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329748313
EC Number:
205-480-7
Beilstein/REAXYS Number:
1749970
MDL number:
MFCD00009446

Key Documents

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InChI key

CQEYYJKEWSMYFG-UHFFFAOYSA-N

InChI

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

SMILES string

CCCCOC(=O)C=C

grade

analytical standard

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

Quality Level

100

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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

signalword

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

3 - Flammable liquids

wgk

WGK 1

flash_point_f

100.4 °F - closed cup

flash_point_c

38 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
BCCN5102
BCCL5319
BCCJ3969
BCCF1959
BCCC6200

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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
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
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
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
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
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