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Sodium acrylate

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Sodium acrylate Basic information

Product Name:
Sodium acrylate
Synonyms:
  • ACRYLIC ACID, SODIUM SALT
  • 2-propenoic acid sodium salt
  • SODIUM ACRYLATE
  • Sodium 2-propenoate
  • SODIUM ACRYLATE ANHYDROUS
  • Propenoic acid sodium salt
  • Sodium propenoate
  • SodiuM acrylate 97%
CAS:
7446-81-3
MF:
C3H3NaO2
MW:
94.04
EINECS:
231-209-7
Mol File:
7446-81-3.mol
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Sodium acrylate Chemical Properties

Melting point:
>300 °C (lit.)
Density 
1.528[at 20℃]
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
solubility 
Aqueous Acid (Slightly), Methanol (Slightly), Water (Slightly)
form 
Solid
color 
White to Off-White
Water Solubility 
479g/L at 20℃
Hydrolytic Sensitivity
0: forms stable aqueous solutions
Stability:
May be unstable; may spontaneously polymerize. Incompatible with strong oxidizing agents.
InChI
InChI=1S/C3H4O2.Na/c1-2-3(4)5;/h2H,1H2,(H,4,5);/q;+1/p-1
InChIKey
NNMHYFLPFNGQFZ-UHFFFAOYSA-M
SMILES
C([O-])(=O)C=C.[Na+]
LogP
0.46 at 25℃
CAS DataBase Reference
7446-81-3(CAS DataBase Reference)
EPA Substance Registry System
Sodium acrylate (7446-81-3)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
RIDADR 
UN 3077 9 / PGIII
WGK Germany 
3
TSCA 
Yes
HS Code 
29161100
Hazardous Substances Data
7446-81-3(Hazardous Substances Data)

MSDS

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Sodium acrylate Usage And Synthesis

Chemical Properties

Colorless or light yellow viscous liquid, non-toxic, weakly alkaline, insoluble in organic solvents such as ethanol, acetone, etc., easily soluble in water and aqueous sodium hydroxide, but in aqueous solutions such as calcium hydroxide, magnesium hydroxide, etc., with the increase in the number of alkaline-earth metal ions, the first to dissolve and then precipitate.

Uses

Sodium Acrylate (SA) is a sodium salt of acrylic acid with antibacterial properties. Sodium polyacrylate is a sodium salt of a polymer consisting of acrylic acid, methacrylic acid or one of their simple esters. SA can be used in tuning the grain size of iron oxide microparticles for potential applications in biological assaying and in chemical sensors. Additionally, it acts as a reducing and capping agent for gold nanoparticles, beneficial for various biological applications.

benefits

Sodium acrylate is the sodium salt of acrylic acid. In Skincare or personal care products, sodium acrylate is often used as an ingredient with specific properties, such as its ability to act as a thickening agent or stabilizer in formulations, contributing to the overall texture and stability of the product.
Thickening Agent:Sodium acrylate is commonly used as a thickening agent in cosmetic formulations. It helps improve the viscosity and texture of the product, giving it a smooth and luxurious feel. This is particularly important for products like creams, lotions, and gels.
Stabilizer:Sodium acrylate can contribute to the stability of formulations. It helps prevent the separation of ingredients and enhances the overall shelf life of the product. This is important for maintaining the efficacy and quality of skincare products over time.
Enhanced Spreadability:The inclusion of sodium acrylate in formulations can improve the spreadability of skincare products on the skin. This ensures even application and distribution of the product, enhancing the user experience.
Film-Forming Properties:In some formulations, sodium acrylate may have film-forming properties. This can create a thin film on the skin, providing a protective barrier and potentially helping to lock in moisture.

General Description

Sodium acrylate (SA) is a metal salt that can be prepared by an acid-base reaction between sodium hydroxide and acrylic acid. It can be used in the preparation of poly(sodium acrylate) using bulk, solution, emulsion, and suspension polymerization techniques. It results in the formation of a water soluble polymer that can be used in a variety of industries and personal care applications.

Flammability and Explosibility

Non flammable

Synthesis

An aqueous solution of sodium acrylate is prepared from 216.2 g of acrylic acid (100%=3 mol), 262.8 g of NaOH (50%) and 497 g of water. 3.7 g of N-nitrosodiphenylamine and 3.7 g of 4-methoxyphenol are added to stabilize the solution. 12 g of the quaternary ammonium salt used in Example 1 are also added. 1,125 g (9 mol) of 1,4-dichlorobutene are run in at 90° C. 15.9 g of Na2CO3 are added after 1 hour and the mixture is left to react for a further 2 hours at 90° C. After phase separation, the organic layer is distilled under vacuum. 286.0 g (1.78 mol) of 4-chloro-2-butenyl acrylate (59.4% of the theoretical yield) are obtained. 641 g (5.13 mol) of dichlorobutene are recovered.

References

[1] SIMONE MANZINI . Palladium- and Nickel-Catalyzed Synthesis of Sodium Acrylate from Ethylene, CO2, and Phenolate Bases: Optimization of the Catalytic System for a Potential Process[J]. European Journal of Organic Chemistry, 2015, 2015 32: Pages 7122-7130. DOI:10.1002/ejoc.201501113.
[2] KALRA B, GROSS R A. HRP-mediated polymerizations of acrylamide and sodium acrylate[J]. Green Chemistry, 2002, 2: 174-178. DOI:10.1039/B106735B.
[3] https://www.ewg.org/skindeep/ingredients/705976-SODIUM_ACRYLATES_COPOLYMER/

Sodium acrylate Preparation Products And Raw materials

Preparation Products

Sodium acrylateSupplier

Hebei Zhentian Food Additives Co., Ltd. Gold
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0319-5925599 13373390591
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13933732699@163.com
Guangzhou Yunmen Biotechnology Co., Ltd Gold
Tel
18902340307 18902340307
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3356812514@qq.com
Beijing Solarbio Science & Tecnology Co., Ltd. Gold
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010-50973130 17801761073
Email
Gsiyu@solarbio.com
Nanjing shengyilai Chemical Co., Ltd Gold
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19951936396
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3158688292@qq.com
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
021-61259108 18621169109
Email
market03@meryer.com