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4-PHENYLENEDIACRYLIC ACID

CAS No.
16323-43-6
Chemical Name:
4-PHENYLENEDIACRYLIC ACID
Synonyms
NSC 133919;RARECHEM AL BK 0108;P-PHENYLENEDIACRYLIC ACID;TEREPHTHALDICINNAMIC ACID;1,4-BENZENEDIACRYLIC ACID;4-PHENYLENEDIACRYLIC ACID;1,4-PHENYLENEDIACRYLIC ACID;p-Phenylenebis[acrylic acid];p-Phenylenediacrylic acid,97%;1,4-Benzenediacrylic acid-98%
CBNumber:
CB6712491
Molecular Formula:
C12H10O4
Molecular Weight:
218.21
MDL Number:
MFCD00002698
MOL File:
16323-43-6.mol
MSDS File:
SDS
Last updated:2024-12-18 14:15:30

4-PHENYLENEDIACRYLIC ACID Properties

Melting point >300 °C(lit.)
Boiling point 318.88°C (rough estimate)
Density 1.358
refractive index 1.7160 (estimate)
storage temp. Sealed in dry,Room Temperature
pka -95.84±0.10(Predicted)
form powder to crystal
color White to Light yellow
BRN 2579464
CAS DataBase Reference 16323-43-6(CAS DataBase Reference)
FDA UNII 0F7E4O8Q8Y
EPA Substance Registry System p-Phenylenediacrylic acid (16323-43-6)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P280a-P304+P340-P305+P351+P338-P405-P501a
Risk Statements  36/37/38
Safety Statements  24/25
WGK Germany  3
TSCA  Yes
HS Code  29173990
NFPA 704
0
1 0

4-PHENYLENEDIACRYLIC ACID price More Price(13)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich P23903 1,4-Phenylenediacrylic acid 97% 16323-43-6 5g $83.2 2024-03-01 Buy
TCI Chemical P1309 1,4-Phenylenediacrylic Acid 16323-43-6 1G $16 2024-03-01 Buy
TCI Chemical P1309 1,4-Phenylenediacrylic Acid 16323-43-6 5G $46 2024-03-01 Buy
Alfa Aesar L01141 1,4-Benzenediacrylic acid, 98% 16323-43-6 5g $43.65 2024-03-01 Buy
Alfa Aesar L01141 1,4-Benzenediacrylic acid, 98% 16323-43-6 25g $135 2021-12-16 Buy
Product number Packaging Price Buy
P23903 5g $83.2 Buy
P1309 1G $16 Buy
P1309 5G $46 Buy
L01141 5g $43.65 Buy
L01141 25g $135 Buy

4-PHENYLENEDIACRYLIC ACID Chemical Properties,Uses,Production

Chemical Properties

YELLOW POWDER

General Description

Yellow powder or solid.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

1,4-PHENYLENEDIACRYLIC ACID is a carboxylic acid. Carboxylic acids donate hydrogen ions if a base is present to accept them. They react in this way with all bases, both organic (for example, the amines) and inorganic. Their reactions with bases, called "neutralizations", are accompanied by the evolution of substantial amounts of heat. Neutralization between an acid and a base produces water plus a salt. Carboxylic acids with six or fewer carbon atoms are freely or moderately soluble in water; those with more than six carbons are slightly soluble in water. Soluble carboxylic acid dissociate to an extent in water to yield hydrogen ions. The pH of solutions of carboxylic acids is therefore less than 7.0. Many insoluble carboxylic acids react rapidly with aqueous solutions containing a chemical base and dissolve as the neutralization generates a soluble salt. Carboxylic acids in aqueous solution and liquid or molten carboxylic acids can react with active metals to form gaseous hydrogen and a metal salt. Such reactions occur in principle for solid carboxylic acids as well, but are slow if the solid acid remains dry. Even "insoluble" carboxylic acids may absorb enough water from the air and dissolve sufficiently in 1,4-PHENYLENEDIACRYLIC ACID to corrode or dissolve iron, steel, and aluminum parts and containers. Carboxylic acids, like other acids, react with cyanide salts to generate gaseous hydrogen cyanide. The reaction is slower for dry, solid carboxylic acids. Insoluble carboxylic acids react with solutions of cyanides to cause the release of gaseous hydrogen cyanide. Flammable and/or toxic gases and heat are generated by the reaction of carboxylic acids with diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, and sulfides. Carboxylic acids, especially in aqueous solution, also react with sulfites, nitrites, thiosulfates (to give H2S and SO3), dithionites (SO2), to generate flammable and/or toxic gases and heat. Their reaction with carbonates and bicarbonates generates a harmless gas (carbon dioxide) but still heat. Like other organic compounds, carboxylic acids can be oxidized by strong oxidizing agents and reduced by strong reducing agents. These reactions generate heat. A wide variety of products is possible. Like other acids, carboxylic acids may initiate polymerization reactions; like other acids, they often catalyze (increase the rate of) chemical reactions.

Fire Hazard

Flash point data for 1,4-PHENYLENEDIACRYLIC ACID are not available; however, 1,4-PHENYLENEDIACRYLIC ACID is probably combustible.

127-09-3
623-27-8
16323-43-6
23359-08-2
Synthesis of 4-PHENYLENEDIACRYLIC ACID from Sodium acetate and Terephthalaldehyde
Global( 111)Suppliers
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Hebei Weibang Biotechnology Co., Ltd
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View Lastest Price from 4-PHENYLENEDIACRYLIC ACID manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
(2E,2'E)-3,3'-(1,4-Phenylene)bisacrylic acid pictures 2023-02-13 (2E,2'E)-3,3'-(1,4-Phenylene)bisacrylic acid
16323-43-6
US $10.00 / KG 1KG 99% 50MT Hebei baicao biology science and technology co., ltd
4-PHENYLENEDIACRYLIC ACID pictures 2020-01-03 4-PHENYLENEDIACRYLIC ACID
16323-43-6
US $1.00 / KG 1KG 99% 200kg Career Henan Chemical Co
1,4-Phenylenediacrylic acid 97% 3-(3-oxo-2,3-dihydro-1H-inden-5-yl)propanoic acid 3,3’-(1,4-phenylene)bis-2-propenoicaci 1,4-PHENYLENEDIACRYLIC ACID 1,4-BENZENEDIACRYLIC ACID RARECHEM AL BK 0108 TEREPHTHALDICINNAMIC ACID P-PHENYLENEDIACRYLIC ACID 3,3'-(p-phenylene)diacrylic acid 3314PHENYLENEBIS2PROPENOICACID 3,3'-(1,4-Phenylene)dipropenoic acid p-Phenylenediacrylic acid,97% NSC 133919 p-Phenylenebis[acrylic acid] trans,trans-1,4-Phenylenediacrylic acid 4-PHENYLENEDIACRYLIC ACID 3-[2-(2-carboxyethenyl)phenyl]-2-propenoic acid 2-Propenoic acid, 3,3'-(1,4-phenylene)bis- 4-PHENYLENEDIACRYLIC ACID USP/EP/BP 1,4-Benzenediacrylic acid-98% (2E,2'E)-3,3'-(1,4-Phenylene)bisacrylic acid 16323-43-6 C6H4CHCHCO2H2 Organic Building Blocks Building Blocks Carboxylic Acids Carbonyl Compounds C11 to C12 Aromatic Cinnamic Acids, Esters and Derivatives C11 to C12 Carbonyl Compounds Carboxylic Acids Building Blocks C11 to C12 Carbonyl Compounds Carboxylic Acids Chemical Synthesis Organic Building Blocks