6025-45-2 Usage
Uses
Used in Pharmaceutical Industry:
Disodium benzene-1,3-diolate is used as a reducing agent and antioxidant for its ability to neutralize free radicals and protect the active ingredients in pharmaceutical formulations, thereby extending their shelf life and maintaining their efficacy.
Used in Topical Medications:
In topical medications, disodium benzene-1,3-diolate is used as a preservative to prevent oxidation and degradation of the medication's active components, ensuring the product's stability and effectiveness over time.
Used in Beauty Products:
Disodium benzene-1,3-diolate is used as an antioxidant in beauty products to protect the skin from the harmful effects of free radicals, which can cause damage and premature aging. It also helps to maintain the stability and effectiveness of the product's active ingredients.
Used as a Food Additive:
In the food industry, disodium benzene-1,3-diolate is used as an additive to prevent oxidation and spoilage, helping to maintain the quality and freshness of food products.
Used in Photography:
Although not explicitly mentioned in the provided materials, disodium benzene-1,3-diolate may have potential applications in the photography industry, likely due to its reducing properties, which could be useful in the development and preservation of photographic materials.
Used in Polymer Manufacturing:
Similarly, while not detailed in the materials, disodium benzene-1,3-diolate may also find use in the polymer manufacturing industry, potentially for its antioxidant properties to enhance the stability and longevity of polymer products during production or storage.
Check Digit Verification of cas no
The CAS Registry Mumber 6025-45-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,2 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6025-45:
(6*6)+(5*0)+(4*2)+(3*5)+(2*4)+(1*5)=72
72 % 10 = 2
So 6025-45-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H6O2.2Na/c7-5-2-1-3-6(8)4-5;;/h1-4,7-8H;;/q;2*+1/p-2
6025-45-2Relevant articles and documents
Synthesis and group 9 complexes of macrocyclic PCP and POCOP pincer ligands
Chaplin, Adrian B.,Gyton, Matthew R.,Leforestier, Baptiste
, p. 2087 - 2101 (2020/02/26)
The synthesis of macrocyclic variants of commonly employed phosphine-based pincer (pro)ligands derived from meta-xylene (PCP-14) and resorcinol (POCOP-14) is described, where the P-donors are trans-substituted with a tetradecamethylene linker. The former
Process for preparing dibasic salts of bisphenols
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Page/Page column 4, (2008/06/13)
The present invention discloses a process for preparing dibasic salt of bisphenol from bisphenol and alkali, wherein the bisphenol and the alkali are reacted in a reaction medium consisting of an organic solvent or an aqueous inorganic salt solution, and then through filtration, a highly pure dibasic salt of bisphenol is directly obtained at a yield of higher than 90%.
2-[16-(3-fluoro-5-trifluoromethyl-pyridinyl-2-oxy)-3-nitro-phenoxy]-propionic acid derivatives, herbicidal compositions containing same and herbicidal method of use
-
, (2008/06/13)
Novel compounds, e.g., N-methanesulfonyl 2-((5-(3-fluoro-5-(trifluoromethyl)-2-pyridinyl)oxy)-2-nitro-5-phenoxy)propionamide are selective herbicides useful for controlling weeds in valuable crops.
