What is the Carbomer?

Carbomer is white powder, while it's Molecular Formula is -[-CH2-CH-]N-COOH. white powder Used in Superabsorbent Applications: Carbomer is used as a superabsorbent for its ability to absorb and retain water, swelling to many times its original volume. This property makes it ideal for applications where water absorption and retention are crucial. Used in Detergents and Dispersants: Carbomer is used as an ingredient in detergents and dispersants, accounting for about 25% of its total usage. Its water-absorbing and polyelectrolyte properties contribute to the effectiveness of these products. Used in Disposable Diapers: Carbomer is used in the production of disposable diapers, where its superabsorbent qualities help to manage and retain liquid, providing comfort and functionality to the user. Used in Superabsorbent Polymers (SAPs): Carbomer is a key component of Superabsorbent Polymers (SAPs), which are cross-linked polyacrylates capable of absorbing and retaining more than 100 times their own weight in liquid. These polymers are widely used in various applications due to their exceptional water-absorbing capabilities. Used in Hydrogels for Wound Healing: Hydrogels derived from Carbomer have been extensively studied for their potential use as bandages and aids for wound healing. The water-attracting and acid-base properties of Carbomer make it a suitable candidate for these medical applications, where effective management of moisture and interaction with biological tissues are essential.

What is the CAS number for Carbomer?

The CAS number of Carbomer is 54182-57-9.

What is Carbomer (54182-57-9) used for?

Carbomer is a polymer with the formula (CH2-CHCO2H)n. It is a derivative of acrylic acid (CH2=CHCO2H). In addition to the homopolymers, a variety of copolymers and crosslinked polymers, and partially deprotonated derivatives thereof are known and of commercial value. In a water solution at neutral pH, PAA is an anionic polymer, i.e., many of the side chains of PAA lose their protons and acquire a negative charge. Partially or wholly deprotonaated PAAs are polyelectrolytes, with the ability to absorb and retain water and swell to many times their original volume. These properties - acid-base and water-attracting - are the bases of many applications.InChI:InChI=1/C3H4O2/c1-2-3(4)5/h2H,1H2,(H,4,5)

What is the Carbomer?

Carbomer is white powder, while it's Molecular Formula is -[-CH2-CH-]N-COOH. white powder Used in Superabsorbent Applications: Carbomer is used as a superabsorbent for its ability to absorb and retain water, swelling to many times its original volume. This property makes it ideal for applications where water absorption and retention are crucial. Used in Detergents and Dispersants: Carbomer is used as an ingredient in detergents and dispersants, accounting for about 25% of its total usage. Its water-absorbing and polyelectrolyte properties contribute to the effectiveness of these products. Used in Disposable Diapers: Carbomer is used in the production of disposable diapers, where its superabsorbent qualities help to manage and retain liquid, providing comfort and functionality to the user. Used in Superabsorbent Polymers (SAPs): Carbomer is a key component of Superabsorbent Polymers (SAPs), which are cross-linked polyacrylates capable of absorbing and retaining more than 100 times their own weight in liquid. These polymers are widely used in various applications due to their exceptional water-absorbing capabilities. Used in Hydrogels for Wound Healing: Hydrogels derived from Carbomer have been extensively studied for their potential use as bandages and aids for wound healing. The water-attracting and acid-base properties of Carbomer make it a suitable candidate for these medical applications, where effective management of moisture and interaction with biological tissues are essential.

What is the CAS number for Carbomer?

The CAS number of Carbomer is 54182-57-9.

What is Carbomer (54182-57-9) used for?

Carbomer is a polymer with the formula (CH2-CHCO2H)n. It is a derivative of acrylic acid (CH2=CHCO2H). In addition to the homopolymers, a variety of copolymers and crosslinked polymers, and partially deprotonated derivatives thereof are known and of commercial value. In a water solution at neutral pH, PAA is an anionic polymer, i.e., many of the side chains of PAA lose their protons and acquire a negative charge. Partially or wholly deprotonaated PAAs are polyelectrolytes, with the ability to absorb and retain water and swell to many times their original volume. These properties - acid-base and water-attracting - are the bases of many applications.InChI:InChI=1/C3H4O2/c1-2-3(4)5/h2H,1H2,(H,4,5)

Product classification

Carbomer

Chemical raw materials, non-pharmaceuticals.
Product Name: Carbomer
CasNo: 54182-57-9
Purity:
Appearance: white powder

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CasNo： 54182-57-9

Appearance： white powder

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Molecular Formula:-[-CH2-CH-]N-COOH
Molecular Weight:0
Appearance/Colour:white powder
Boiling Point:116 °C
PSA：0.00000
Density:1.09 (30% aq.)
LogP:0.00000

Carbomer(Cas 54182-57-9) Usage

Structure

Polyacrylic acid is a polyolefin.?It can be viewed as polyethylene with carboxylic acid (CO2H) substituents on alternating carbons.?Owing to these groups, alternating carbon atoms in the backbone are stereogenic (colloquially: chiral).?For this reason, acrylic acid exists in atactic, syndiotactic, and isotactic forms, although this aspect is rarely discussed.?The polymerization is initiated with radicals and is assumed to be stereorandom.?Crosslinking can be introduced in many ways.

Application

The dominant application for PAA is as a superabsorbent. About 25% of PAA is used for detergents and dispersants.Polyacrylic acid and its derivatives are used in disposable diapers. Acrylic acid is also the main component of Superadsorbent Polymers (SAPs), cross-linked polyacrylates that can absorb and retain more than 100 times of their own weight in liquid. Hydrogels derived from PAA have attracted much study for use as bandages and aids for wound healing.

InChI:InChI=1/C3H4O2/c1-2-3(4)5/h2H,1H2,(H,4,5)

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Carbomer(Cas 54182-57-9) Usage

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