11129-12-7 Usage
Chemical Description
Borate is a compound containing the BO3 group, while diols are organic compounds containing two hydroxyl groups (-OH) in their molecules.
Description
Borate, a salt of boric acid (H3BO3), is a versatile compound with various applications across different industries. It is found in two known types orthoborate and metaborate and is derived from borate minerals like kernite and tincal. Borax, a specific form of borate, is a water-soluble white compound that serves as a source of boron for plants and has numerous uses in agriculture and other industries.
Uses
Used in Agricultural Applications:
Borate is used as a fertilizer to reduce boron deficiency in plants. It is available in various forms, including orthoborate, metaborate, polyborates, boric acid, calcium polyborate (colemanite), sodium tetraborate, solubor, and complex borosilicate (boron frits). Borax, a supplier of micronutrient boron, is applied as a foliar spray or directly to the soil to enhance plant growth and development.
Used in Glass and Ceramic Industries:
Borate, specifically borax, is used as a metallurgical flux in the glass and ceramic industries. It helps lower the melting point of glass and improves its workability, making it easier to shape and form.
Used in Buffer Solutions:
Borate is used as a buffer in various chemical applications, helping to maintain a stable pH level and preventing drastic changes in acidity or alkalinity.
Used as a Mild Alkaline Antiseptic:
Borate, in the form of borax, serves as a mild alkaline antiseptic, which can be used for cleaning and disinfecting purposes.
Used as a Source of Boron Compounds:
Borate is used as a source of boron compounds in various industrial applications, including the production of insulation materials, detergents, and other chemical products.
Used in Weed Control:
Borate has been used for controlling weeds in specific locations. However, the introduction of synthetic organic herbicides, such as 4,6-dinitro-o-cresol (DNOC), has largely replaced borate in this application.
Enzyme inhibitor
This conjugate base (FW = 61.83 g/mol; CAS 11129-12-7) of boric acid is the likely consequence of boric acid acting as a Lewis acid (i.e., as an electron pair acceptor), as does boron trifluoride, to form B(OH)4–. Borate is soluble in cold water (1 g/18 mL) and inhibits many enzymes. The neutral species has been shown to inhibit urease by bridging the enzyme’s pair of catalytic nickel ions. Boric acid also forms a complex with serine that inhibitsγ-glutamyl transpeptidase. (See also Serine-Borate Complex) Sodium borate Na2B4O7, also called sodium tetraborate, is often used as an antiseptic and detergent. The decahydrate is known as Borax. Dionex BorateTrap?: Because borate can be leached from borosilicate laboratory glassware, and because borate binds to vicinal hydroxyl groups in many carbohydrates, one cannot discount the possibility of borate effects on carbohydrate-utilizing enzymes. The Dionex BorateTrap is a 4 × 50 mm column placed between the eluent pump and an HPLC injection valve to remove borate contamination from eluents. Its placed prior the injection valve assures that the trap will have no effect on the efficiencies or retention times of the carbohydrate analytes. The trap itself is packed 20-μm high-capacity resin that has high selectivity for borate. The resin used in the BorateTrap is functionalized with a polyol capable of complexing borate in the presence of hydroxide. The BorateTrap eliminates peak tailing for mannose, fructose, and reduced monosaccharides, resulting from contamination of the eluent from borate. Therefore, the BorateTrap is highly recommended for optimal performance during carbohydrate analysis. Target(s): L-iditol dehydrogenase; deoxyribonuclease I; glycerol-2-phosphatase; 5’- nucleotidase; steryl-sulfatase; aspartate-semialdehyde dehydrogenase; γ-glutamyltransferase, plant; clostripain; Lgulonolactone oxidase; dehydro-L-gulonate decarboxylase; catechol O-methyltransferase; alcohol dehydrogenase; catechol oxidase, or o-diphenol oxidase; arginase; peptide-N4- (N-acetyl-b glucosaminyl)asparagine amidase; glutamyl endopeptidase; glutaminase; alkaline phosphatase; glycogen synthase; xanthine oxidase; carboxypeptidase B, above pH 8; acid phosphatase; glucose-6-phosphatase; urease; formimidoylglutamase, or formimino-glutamase; phosphodiesterase; arylsulfatase A, or cerebroside-sulfatase; arylsulfatase B, or Nacetylgalactosamine-4-sulfatase; cholinesterase; b-lactamase; tyrosinase; glyceraldehyde-3-phosphate dehydrogenase; venom exonuclease; kynureninase, weakly inhibited); tetrahydrofolate synthetase; carboxy-cis,cis-muconate cyclase, under acidic conditions; cyclamate sulfohydrolase; nucleotide diphosphatase; cytidine deaminase; methylenediurea deaminase; allantoate deaminase; 4-methyleneglutaminase; pantothenase; bacterial leucyl aminopeptidase, weakly inhibited; aminopeptidase B; N-acetylgalactosamine-4-sulfatase, or arylsulfatase B; glycosulfatase; steryl-sulfatase, inhibited by metaborate and tetraborate; Arylsulfatase; 3-phosphoglycerate phosphatase; 3- or 4-phytase; alkaline phosphatase; arginine kinase; arginine:pyruvate transaminase; peptidyltransferase, weakly inhibited; protein-histidine N-methyltransferase, weakly inhibited; cyclopropane-fatty-acyl-phospholipid synthase; xanthine oxidase; 4 hydroxybenzoate 3-monooxygenase; lysine 2-monooxygenase; catechol 2,3-dioxygenase; catalase, weakly inhibited; catechol oxidase; polyphenol oxidase
Check Digit Verification of cas no
The CAS Registry Mumber 11129-12-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,1,1,2 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 11129-12:
(7*1)+(6*1)+(5*1)+(4*2)+(3*9)+(2*1)+(1*2)=57
57 % 10 = 7
So 11129-12-7 is a valid CAS Registry Number.
InChI:InChI=1/BO3/c2-1(3)4/q-3
