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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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Thomas Junkers et al.
Macromolecular rapid communications, 33(11), 984-990 (2012-05-05)
A novel dithioester control agent [dimethyltetrathioterephtalate (DMTTT)] is presented for the thioketone-mediated radical polymerization (TKMP) of n-butyl acrylate. The rate of polymerization is significantly decreased in the presence of DMTTT indicating formation of dormant radical species. During polymerization, molar masses
A radio-fluorogenic organic gel for real-time, 3D radiation dosimetry.
John M Warman et al.
Advanced materials (Deerfield Beach, Fla.), 23(42), 4953-4955 (2011-10-13)
Sébastien-Jun Mougnier et al.
Macromolecular rapid communications, 33(8), 703-709 (2012-02-23)
The post-functionalization of poly(3-hexylthiophene) (P3HT) via various synthetic routes is reported. Well-defined and monofunctionalized ω-thiol-terminated P3HT, ω-carboxylic acid-terminated P3HT, ω-acrylate-terminated P3HT, and ω-methacrylate-terminated P3HT are obtained in high yields through a straightforward procedure. From those, different novel P3HT-based graft copolymers
Sabrina Hocine et al.
Langmuir : the ACS journal of surfaces and colloids, 29(5), 1356-1369 (2013-01-09)
Thermoresponsive behavior of different kinds of polymersomes was studied using small angle neutron scattering (SANS), transmission electron microscopy (TEM), and proton nuclear magnetic resonance ((1)H NMR). The polymersomes were made of block copolymers containing a 2000 Da polyethylene glycol (PEG)
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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