Acrylic Acid (99.5%) - China

Acrylic Acid (99.5%) - China

Origin
: India, China
CAS Number
: 79-10-7
HS Code
: 2916.11.00
Basic Info
IUPAC Name
: prop-2-enoic acid
Molecular Formula
: C3H4O2
Molecular Weight (g/mol)
: 72.0600
Synonyms & Trade Names
: Acrylic acid; Propenoic acid; Glacial acrylic acid
Purity / Assay (%)
: 99.5% min
Grade / Quality Level
: Industrial Grade
Physical Form
: Liquid
Concentration
: Pure substance
Appearance / Color
: Clear to slightly colored liquid
Odor
: Pungent, acrylic
Melting Point (°C)
: 14.0000
Boiling Point (°C)
: 141
Density (g/cm³)
: 1.0490
Solubility in Water
: Miscible
Signal Word
: Danger
UN Number
: 2218
GHS Hazard Class
: Flammable; Acute toxic; Skin corrosive; Respiratory sensitizer
H-Statements
: H226|H302|H312|H314|H317|H332|H335
P-Statements
: P210|P260|P264|P271|P272|P273|P280|P301+P330+P331
REACH Status
: Registered
Drug Precursor Status
: Non-precursor
Storage Class (GHS)
: 8
Storage Conditions
: Cool, dark; inhibitor required; away from peroxides
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Technical Document

Brief Overview

Acrylic acid is an unsaturated carboxylic acid, with the formula CH2=CHCO2H. This clear and colourless liquid has a characteristic acrid odour. As it contains a polar carboxylic acid functional group, it is able to dissolve in water and is miscible with relatively polar organic compounds such as alcohols, ethers, and chloroform. Acrylic acid is air and water sensitive as it reacts readily with free radicals and electrophilic or nucleophilic agents. It may polymerise in the presence of acids, alkalis, amines, peroxides, and iron salts. Prolonged exposure to heat or exposure of light can also cause polymerisation. If confined, the polymerisation of acrylic acid can lead to explosion even at room temperature. It is corrosive to metals and tissues.
Acrylic acid can be used in the form of free acids, ammonium and alkali salts in many different applications such as thickeners, dispersing agents, flocculants, wetting agents, coatings, textile finishes protective colloids for stabilizing emulsions and polymer dispersions. It readily undergoes additional reactions with a wide variety of organic and inorganic compounds, which makes it a very useful feedstock for the production of many low molecular compounds. For instance, acrylic acid can be used to produce derivatives of propionic acid with water, alcohols, amines, halogens and chlorinated hydrocarbons. It can also react with other substances to produce unsaturated fatty acids, heterocyclic compounds and Diels-Alder addition products.
As it polymerises with explosive violence, it can only be shipped after being stabilised by an inhibitor such as hydroquinone. The removal of the stabilizer is not usually necessary, since its action can be compensated for by adding an excessive initiator.

Manufacturing Processing

The most widely accepted process for making acrylic acid is the vapour phase oxidation of propylene via acrolein, where propylene is a byproduct of ethylene and gasoline production. Typically, Chemical-Grade (CG) propylene is mixed with steam and air to undergo a two-step oxidation where propylene is oxidised to acrolein before further oxidising again to give acrylic acid. These oxidations are done in tubular, fixed-bed reactors where steam is generated by utilising the heat emitted by the exothermic reactions.