9003-08-1 Usage
Uses
Different sources of media describe the Uses of 9003-08-1 differently. You can refer to the following data:
1. Melamine formaldehyde is used for the treatment of heavy fabrics, draperies, coatings, collars, and apparel; in water- and oil-repellent and flame-retardant
hrllsIies (effective on synthetic and natural fibers).
2. Suggested starting dilutions are as follows: IHC-P: 1:100-1:1000, WB: 1:500-1:3000. Not yet tested in other applications. Optimal working dilutions should be determined experimentally by the end user.
Definition
A type of amino resin made
from melamine and formaldehyde. The first step
in resin formation is the production of trimethylol melamine, C3N3(NHCH2OH)3, the molecules
of which contain a ring with three carbon and
three nitrogen atoms, the –NHCH2OH groups being
attached to the carbon atoms. This molecule can
combine further with others of the same kind by
a condensation reaction. Excess formaldehyde or
melamine can also react with trimethylol melamine
or its polymers, providing many possibilities of
chain growth and cross-linking. The nature and
degree of polymerization depend upon pH, but heat
is always needed for curing. Melamine resins are
more waterand heat-resistant than urea resins.
They may be water-soluble syrups (low molecular weight) or insoluble powders (high molecular weight) dispersible in water. Widely used as
molding compounds with α-cellulose, wood flour,
or mineral powders as fillers and with coloring
materials; also for laminating, boil-proof adhesives,
increasing wet strength of paper, textile treatment,
leather processing, and for dinnerware and decorative plastic items. Butylated melamine resins are
formed by incorporating butyl or other alcohols during resin formation, whereupon the –NHCH2OH
groups convert to –NHCH2OC4H9. These resins are
soluble in paint and enamel solvents and in surface
coatings, often in combination with alkyds. They
give exceptional curing speed, hardness, wear resistance, and resistance to solvents, soaps, and foods.
Melamine-acrylic resins are water soluble and used
for formation of water-base industrial and automotive finishes.
Industrial uses
This is a synthetic resin of the alkyd type madeby reacting melamine with formaldehyde. Theresin is thermosetting, colorless, odorless, andresistant to organic solvents. It is more resistantto alkalies and acids than urea resins, has betterheat and color stability, and is harder. Themelamine resins have the general uses of moldingplastics, and also are valued for dishes forhot foods or acid juices and they will not softenor warp when washed in hot water. Melamine,a trimer of cyanamide, has the composition(NC·NH2)3. The melamine resins have good adhesivenessbut are too hard for use alone in coatingsand varnishes. They are combined with alcoholmodifiedurea-formaldehyde resins to give coatingmaterials of good color, gloss, flexibility, andchemical resistance. Urea-modified melamineformaldehyderesins are used for coatings andvarnishes. Melamine-formaldehyde moldingresin, with cellulose filler, has a tensile strengthof 51 MPa and dielectric strength per mil of12.8×106V/m. Melamine-urea-formaldehyde resin with alignin extender is used as an adhesive for waterresistantplywood. Phenol-modified melamineformaldehyderesin solution is used for laminatingfibrous materials. Highly translucentmelamine-formaldehyde resin is used for moldinghigh-gloss buttons. Methylol-melamine,made by alkylating a melamine-formaldehyderesin with methyl alcohol, is used for shrinkproofingwoolen fabrics.
Biochem/physiol Actions
This gene belongs to the subfamily of small cytokine CC genes. Cytokines are a family of secreted proteins involved in immunoregulatory and inflammatory processes. The CC cytokines are proteins characterized by two adjacent cysteines. The cytokine encoded by this gene displays chemotactic activity for resting CD4 or CD8 T cells and eosinophils. The product of this gene binds to chemokine receptors CCR3 and CCR10. This chemokine may play a role in the physiology of extracutaneous epithelial tissues, including diverse mucosal organs. [provided by RefSeq]
Check Digit Verification of cas no
The CAS Registry Mumber 9003-08-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 9,0,0 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 9003-08:
(6*9)+(5*0)+(4*0)+(3*3)+(2*0)+(1*8)=71
71 % 10 = 1
So 9003-08-1 is a valid CAS Registry Number.
