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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
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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

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.

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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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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
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
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)
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