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About This Item
Linear Formula:
CH2=CHCOOH
CAS Number:
Molecular Weight:
72.06
NACRES:
NA.23
PubChem Substance ID:
eCl@ss:
39021317
UNSPSC Code:
12162002
EC Number:
201-177-9
MDL number:
Beilstein/REAXYS Number:
635743
grade
anhydrous
Quality Level
vapor density
2.5 (vs air)
vapor pressure
4 mmHg ( 20 °C)
assay
99%
form
liquid
autoignition temp.
744 °F
contains
200 ppm MEHQ as inhibitor
expl. lim.
13.7 %
bp
139 °C (lit.)
mp
13 °C (lit.)
density
1.051 g/mL at 25 °C (lit.)
SMILES string
OC(=O)C=C
InChI
1S/C3H4O2/c1-2-3(4)5/h2H,1H2,(H,4,5)
InChI key
NIXOWILDQLNWCW-UHFFFAOYSA-N
General description
Acrylic acid is an unsaturated carboxylic acid that is commonly used as a versatile building block in the chemical industry because of its reactive double bond between the carbon and oxygen atoms. It is used to prepare various acrylic acid-based polymers, which are used for various applications such as adhesives, paints & coatings, medical devices, organic semiconductors,thin-film transistors, hydrogels and lithium-ion batteries. Additionally, acrylic acid also serves as one of the polyelectrolytes in the self-assembled polymeric film used for hydrogen generation.
Application
Acrylic acid can be primarily used as a monomer to produce various acrylic polymers, including polyacrylic acid, polymethyl methacrylate (PMMA), acrylonitrile butadiene styrene (ABS), and many others. These polymers exhibit a wide range of properties, such as transparency, scratch-resistant, flexibility, and resistance to water and chemicals, which make them valuable materials in various applications. Acrylic acid is also used as a key component in the synthesis of superabsorbent polymers(SAPs). These polymers possess a unique ability to quickly absorb and retain large quantities of water. Due to their excellent properties, SAPs have been widely used in many fields, such as drug-delivery systems, chemical industry, and personal care, etc.
Acrylic acid can also be used as:
Acrylic acid can also be used as:
- A key component in the preparation of copolymer binder, which helps to optimize the performance of lithium-ion batteries.
- A surface modifier for the carbon nanotubes with poly(acrylic acid) in order to improve adhesion and dispersion of the nanotubes in the oxide semiconductor matrix for thin-film transistor applications.
- A reactive monomer for the surface modification of polydimethylsiloxane (PDMS)through a simultaneous polymerization process with ethylene glycol dimethacrylate. Modified PDMS potentially applied in new applications fields such as microfluidics or biomedical devices.
- A precursor for the synthesis of cashew gum/acrylic acid nanoparticles via the copolymerization process. The use of acrylic acid in the synthesis is to introduce hydrophilic functional groups into the cashew gum backbone, thereby improving its solubility in water and increasing its compatibility with other hydrophilic materials.
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signalword
Danger
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1A - STOT SE 3
target_organs
Respiratory system
Storage Class
3 - Flammable liquids
wgk
WGK 2
flash_point_f
119.3 °F - closed cup
flash_point_c
48.5 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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Lei Ying et al.
Biomacromolecules, 4(1), 157-165 (2003-01-14)
Surface modification of argon-plasma-pretreated poly(ethylene terephthalate) (PET) films via UV-induced graft copolymerization with acrylic acid (AAc) was carried out. Galactosylated surfaces were then obtained by coupling a galactose derivative (1-O-(6'-aminohexyl)-D-galactopyranoside) to the AAc graft chains with the aid of a
Influence of charge density on the swelling of colloidal poly (< i> N</i>-isopropylacrylamide-co-acrylic acid) microgels.
Kratz K, et al.
Colloids and Surfaces. A, Physicochemical and Engineering Aspects, 170(2), 137-149 (2000)
Loredana Detomaso et al.
Biomaterials, 26(18), 3831-3841 (2005-01-01)
Continuous and modulated glow discharges were used to deposit thin films from acrylic acid vapors. Different deposition regimes were investigated, and their effect on chemical composition, morphology and homogeneity of the coatings, as well as on their stability in water



