Cresolphthalein
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''o''-Cresolphthalein is a
phthalein dye Phthalein dyes are a class of dyes mainly used as pH indicators, due to their ability to change colors depending on pH. They are formed by the reaction of phthalic anhydride with various phenols. They are a subclass of triarylmethane dyes. Common ...
used as a
pH indicator A pH indicator is a halochromism, halochromic chemical compound added in small amounts to a Solution (chemistry), solution so the pH (acidity or Base (chemistry), basicity) of the solution can be determined visually or spectroscopically by chang ...
in
titration Titration (also known as titrimetry and volumetric analysis) is a common laboratory method of Quantitative research, quantitative Analytical chemistry, chemical analysis to determine the concentration of an identified analyte (a substance to be ...
s. It is insoluble in water but soluble in
ethanol Ethanol (also called ethyl alcohol, grain alcohol, drinking alcohol, or simply alcohol) is an organic compound with the chemical formula . It is an Alcohol (chemistry), alcohol, with its formula also written as , or EtOH, where Et is the ps ...
. Its solution is colourless below pH 8.2, and purple above 9.8. Its molecular formula is C22H18O4. It is used medically to determine calcium levels in the human body, or to synthesize polyamides or polyimides.


Production

o-Cresolphthalein is not produced industrially, rather, it is commercially available. To be produced, the method generally used to synthesize phthalein dyes is effective. This method is used to synthesize
phenolphthalein Phenolphthalein ( ) is a chemical compound with the chemical formula, formula carbon, C20hydrogen, H14oxygen, O4 and is often written as "HIn", "HPh", "phph" or simply "Ph" in shorthand notation. Phenolphthalein is often used as an indicator in ...
and
thymolphthalein Thymolphthalein is a phthalein dye used as an acid– base ( pH) indicator. Its transition range is around pH 9.3–10.5. Below this pH, it is colorless; above, it is blue. The molar extinction coefficient In chemistry, the molar absorption c ...
. To begin, a 2M equivalent of a
phenol Phenol (also known as carbolic acid, phenolic acid, or benzenol) is an aromatic organic compound with the molecular formula . It is a white crystalline solid that is volatile and can catch fire. The molecule consists of a phenyl group () ...
or a substituted phenol should be combined with a 1M equivalent of a
phthalic anhydride Phthalic anhydride is the organic compound with the formula C6H4(CO)2O. It is the anhydride of phthalic acid. Phthalic anhydride is a principal commercial form of phthalic acid. It was the first anhydride of a dicarboxylic acid to be used commer ...
.


Uses

The compound has uses ranging from medicine to laboratory syntheses of chemically similar compounds. o-Cresophthalein has been used to derive
polyamide A polyamide is a polymer with repeating units linked by amide bonds. Polyamides occur both naturally and artificially. Examples of naturally occurring polyamides are proteins, such as wool and silk. Artificially made polyamides can be made throug ...
s and
polyimide Polyimide (sometimes abbreviated PI) is a monomer containing imide groups belonging to the class of high-performance plastics. With their high heat-resistance, polyimides enjoy diverse applications in roles demanding rugged organic materials, suc ...
s, colorimetrically estimate
calcium Calcium is a chemical element; it has symbol Ca and atomic number 20. As an alkaline earth metal, calcium is a reactive metal that forms a dark oxide-nitride layer when exposed to air. Its physical and chemical properties are most similar to it ...
in serum, and predict amount of time to wait before blood collection after a patient receives
gadodiamide Gadodiamide, sold under the brand name Omniscan, is a gadolinium-based MRI contrast agent (GBCA), used in magnetic resonance imaging (MRI) procedures to assist in the visualization of blood vessels. Medical uses Gadodiamide is a contrast ...
.


Deriving Polyamides and Polyimides

Aromatic polyamides and polyamides are practical compounds due to their temperature resistance, electrical or insulating characteristics, and their mechanical strength. Some of the polyamides and polyimides that can be synthesized by o-Cresophthalein are
polycarbonate Polycarbonates (PC) are a group of thermoplastic polymers containing carbonate ester, carbonate groups in their chemical structures. Polycarbonates used in engineering are strong, toughness, tough materials, and some grades are optically transp ...
,
polyacrylate An acrylate polymer (also known as acrylic or polyacrylate) is any of a group of polymers prepared from acrylate monomers. These plastics are noted for their transparency, resistance to breakage, and elasticity. Acrylate polymer is commonly used ...
, and epoxy-resin. The diether-diamine 3,3-bis -(4-amino-phenoxy)-3-methylphenylhthalide, or BNMP, is synthesized by 12 g o-cresophthalein, 11.5 g ''p''-chloronitrobenzene, 5.1 g anhydrous potassium carbonate, and 55 mL of DMF. The compounds should be refluxed together at 160 °C for eight hours. Once it is done and has cooled, it should be mixed with 0.3 L methanol. A precipitate should form and be vacuum filtered to obtain a solid. It should then be washed with water and dried, yielding a yellow product. It should then be recrystallized from glacial acetic acid to yield yellow needles. The product is BNMP. The reaction can go further by combining 15.5 g of BNMP with 0.18 g 10% Pd/C and 50 mL ethanol. They should be stirred at 80 °C. 7 mL of hydrazine monohydrate should be added drop by drop for one hour. The solution should then be mixed for eight hours. It should then be filtered to separated from the Pd/C and concentrated. The concentrated solution should be added to water, and a precipitate should be formed. It should then be vacuum filtered to isolate the solid, yelding 3,3-Bis -(4-aminophenoxy)-3-methylphenylthalide, or BAMP, as a white solid. It should then be purified by water and ethanol.


Colorimetric Estimation of Calcium in Serum

Calcium in a blood sample should be estimated when required medically. Calcium should be precipitated out of 0.1 mL of the blood sample serum as calcium oxalate. After that, the decomposition of the calcium oxalate should occur by heat. Then, the sample should be estimated colorimetrically by o-cresolphthalein complexone. The required liquid complexone is made by dissolving 10 mg o-cresolphthalein complexone in 50 mL alkaline borate, and then 50 mL of 0.05 N HCl are added to make the solution's pH 8.5. This method for calcium determination is efficient and effective, requiring a minimal amount of blood serum sample and a reasonable amount of time.


Determination of Impact of Gadodiamide on Calcium Measurements

Gadolinium is given to patients for magnetic resonance imaging, or an MRI.It is used as a contrast agent for the exam to improve clarity of the images formed. However, it can react in the human body and have detrimental effects. Therefore, the agent should be removed. One of these gadolinium based agents is gadodiamide. Calcium in the body should be determined accurately to ensure that the Gadodiamide does not have adverse effects on the patient. There are two o-cresolphthalein methods to determine amount of calcium. The o-cresolpthalein methods are effective because it is a calcium binding dye. The gadolinium ion with a charge of +3 can be removed from gadodiamide using o-cresolphthalein. For these methods, glomerular filtration rate, or GFR, and time since gadodiamide was given should be recorded. Ultimately, these two factors and the impact of gadodiamide on calcium levels calculated by the o-cresolphthalein method helps to reveal an amount of time that patients must wait after receiving gadodiamide to have blood drawn again, or avoid pseudohypocalcemia.


Safety


NFPA Diamond

To the left is the NFPA diamond as determined by the Safety Data Sheet, or SDS, by Fisher Scientific. There is minimal risk in handling the chemical.


References


External links

*https://web.archive.org/web/20150924095330/http://www.sciencelab.com/msds.php?msdsId=9923574 *http://www.chemicaldictionary.org/dic/O/o-Cresolphthalein_1298.html *http://www.chemspider.com/Chemical-Structure.62217.html {{DEFAULTSORT:Cresolphthalein2 PH indicators Triarylmethane dyes