Carbomer Property

Boiling point:

116 °C

Density 

1.2 g/mL at 25 °C

refractive index 

n20/D 1.442

SMILES

C(C(*)*)(=O)O |$;;*;*;;$|

EPA Substance Registry System

Carbomer (9007-20-9)

Safety

Hazard Codes 

C

Risk Statements 

45-46

Safety Statements 

53-45

RIDADR 

UN 3265 8/PG 3

WGK Germany 

3

RTECS 

AT4680000

Hazard and Precautionary Statements (GHS)

Carbomer Chemical Properties,Usage,Production

Description

Poly(acrylic acid) (PAA; trade name 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.

Chemical Properties

"wets" very quickly

Uses

cosmetic uses e.g., clear gels, hydro-alcoholic gels, lotions and creams

Uses

Carbomers are acrylic acid polymers that are used for a variety of purposes. They are used in pharmaceutical processes as suspending agents, gel bases, emulsifiers, and binding agents. They are also used as artificial tears. Carbomer 974P is a carbomer that is the major non-aqueous component (5% polymer, 94% water) of a proprietary formulation called BufferGel, which also contains dibasic potassium phosphate, magnesium sulfate, dibasic sodium phosphate, sorbic acid, monobasic sodium phosphate, and disodium EDTA. It is a buffering agent, a microbicide, and a spermicide. It is formulated in an aqueous gel at pH 3.9, which acidifies twice its volume of semen to a pH of 5 and maintains the protective acidity of the vagina. It is used vaginally as a spermicide that also protects against HIV infection and possibly other sexually transmitted diseases.

Uses

Poly(Acrylic Acid) is a thickening, suspending, dispersing, emulsifying agent. In the cosmetic and textile printing fields, in printing inks, in emulsion-based lubricants, in pharmaceuticals, polishes, waxes, paints, waterproof and oil-proof coatings, in industrial specialties.

Uses

antiglaucoma agent

Application

Carbomers are thickening agents that help control the viscosity and flow of cosmetic products. They also help distribute and suspend insoluble solids into liquid, and prevent the oil and liquid parts of a solution from separating. They have the ability to absorb and retain water, and can swell up to 1000 times their original volume when dispersed in water. Generally, this class of ingredients is used in gel-like formulations because it forms a colloidal, mucilage-like consistency when mixed in water.
This ingredient is contained in a wide range of personal care products such as styling gel, facial moisturizer, sunscreen, shampoo, anti-aging treatment, eye cream, cleanser and scrubs.

brand name

Carbopol 934P (Noveon); Carbopol 974P (Noveon).

Side effects

irritation. Uncommon side effects (may affect up to 1 in 100 people): eye swelling, eye pain, itchy eye, eye redness, increased tear production.

Safety

The safety of carbomers has been assessed by the Cosmetic Ingredient Review Expert Panel, a group responsible for evaluating the safety of skincare and cosmetics. Carbomer polymers demonstrated a low potential for phototoxicity, photo-contact allergenicity, skin irritation and sensitization at concentrations up to 100%. Upon evaluation of the scientific data, the CIR Expert Panel concluded that carbomer polymers were safe as ingredients in cosmetics and personal care products.

Synthesis

Precipitation polymerization: Carbomers are synthesized by free radical precipitation polymerization conducted in organic solvents. The solvents for this process are selected such that the monomers,  initiators and other additives are soluble in the reaction medium, but  the resulting polymer product is not.