Tannic Acid
(Tannin)
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Tartaric Acid,
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Add the following:
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Butyl Alcohol, Tertiary,
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Change to read:
Testosterone Benzoate,
![]() ![]() C26H32O3 ![]()
2¢,4¢,5¢,7¢-Tetrabromofluorescein
(Eosin Y, Eosin Yellowish, Eosin Bromo ES, Solvent Red 43, Acid Red 87),
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Tetrabromophenolphthalein Ethyl Ester,
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Tetrabutylammonium Bromide,
![]() ![]() ![]() ![]()
Tetrabutylammonium Hydrogen Sulfate,
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Assay—
Dissolve about 170 mg, accurately weighed, in 40 mL of water. Titrate with 0.1 N sodium hydroxide VS, determining the endpoint potentiometrically. Perform a blank determination and make any necessary correction. Each mL of 0.1 N sodium hydroxide is equivalent to 33.95 mg of C16H37NO4S. Not less than 97.0% is found.
Melting range
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Tetrabutylammonium Hydrogen Sulfate Ion Pairing Reagent
—A mixture of tetrabutylammonium hydrogen sulfate and phosphate buffer. Use a suitable grade.
[Note—A suitable grade is available as catalog number WAT084189 from the Waters Corporation (www.waters.com). ]
0.4 M Aqueous Tetrabutylammonium Hydroxide,
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[Note—A suitable grade is available as catalog number 420120025 from www.fishersci.com. ]
Tetrabutylammonium Hydroxide, 1.0 M in Methanol
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Tetrabutylammonium Hydroxide 30-Hydrate,
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Tetrabutylammonium Hydroxide, 40 Percent in Water,
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Tetrabutylammonium Iodide,
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Assay—
Dissolve 370 mg, accurately weighed, in 60 mL of acetone with vigorous stirring. Stir the solution by mechanical means, add 10 mL of 16% sulfuric acid, and titrate with 0.1 N silver nitrate VS, determining the endpoint potentiometrically, using a glass–silver electrode system, and adding the titrant in 0.1-mL increments as the endpoint is approached. Perform a blank determination, and make any necessary corrections. Each mL of 0.1 N silver nitrate is equivalent to 36.94 mg of (C4H9)4NI: not less than 99.0% is found.
Tetrabutylammonium Phosphate,
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Assay—
Dissolve about 1.5 g, accurately weighed, in 100 mL of water. Without delay, titrate with 0.5 N sodium hydroxide VS, determining the endpoint potentiometrically. Perform a blank determination, and make any necessary correction. Each mL of 0.5 N sodium hydroxide is equivalent to 169.7 mg of (C4H9)4NH2PO4. Not less than 97.0% is found.
Add the following:
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2,3,7,8-Tetrachlorodibenzo-p-dioxin, 13C-labeled,
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Assay—
Inject an appropriate volume into a gas chromatograph (see Chromatography
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[Note—A suitable grade is available from Cambridge Isotopes Laboratories (www.isotope.com). ]
2,3,7,8-Tetrachlorodibenzofuran, 13C-labeled,
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Assay—
Inject an appropriate volume into a gas chromatograph (see Chromatography
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[Note—A suitable grade is available from Cambridge Isotopes Laboratories (www.isotope.com). ]
1,1,2,2-Tetrachloroethane,
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Tetradecane,
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Assay—
When examined by gas-liquid chromatography, it shows a purity of not less than 98%. The following conditions have been found suitable for assaying the reagent: a 3-mm × 2.4-m stainless steel column packed with phase G16 on support S1; the carrier gas is helium, flowing at a rate of 27.5 mL per minute; the column temperature is maintained at 250
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Melting range, Class II
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Refractive index
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Tetraethylammonium Perchlorate,
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Tetraethylene Glycol,
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Assay—
When examined by gas–liquid chromatography, using suitable gas chromatographic apparatus and conditions, it shows a purity of not less than 90%.
Boiling range (Reagent test):
between 177
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Tetraethylenepentamine,
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Assay—
Inject an appropriate volume into a gas chromatograph (see Chromatography
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Refractive index
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Tetraheptylammonium Bromide,
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Melting range
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Tetrahexylammonium Hydrogen Sulfate,
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Delta-8-tetrahydrocannabinol (D-8-Tetrahydrocannabinol),
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Tetrahydrofuran,
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Tetrahydrofuran, Peroxide-Free,
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Peroxide—
Transfer 8 mL of potassium iodide and starch TS to a 12-mL ground glass-stoppered cylinder about 15 mm in diameter. Fill completely with the substance under test, mix, and allow to stand protected from light for 5 minutes. No color develops.
Tetrahydrofuran, Stabilizer-Free—
Use a suitable grade.
Tetrahydro-2-furancarboxylic Acid
(±Tetrahydro-2-furoic Acid),
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N-(2-Tetrahydrofuroyl)piperazine
(1-[(Tetrahydro-2-furanyl)carbonyl]piperazine),
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[Note—A suitable grade can be obtained from EMS-DOTTIKON, www.ems-dottikon.ch. ]
1,2,3,4-Tetrahydronaphthalene,
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Refractive index
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Tetramethylammonium Bromide,
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Tetramethylammonium Chloride,
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Assay—
Transfer about 200 mg, accurately weighed, to a beaker, add 50 mL of water and 10 mL of diluted nitric acid, swirl to dissolve the test specimen, add 50.0 mL of 0.1 N silver nitrate VS, and mix. Add 2 mL of ferric ammonium sulfate TS and 5 mL of nitrobenzene, shake, and titrate the excess silver nitrate with 0.1 N ammonium thiocyanate VS: each mL of 0.1 N silver nitrate is equivalent to 10.96 mg of (CH3)4NCl. Not less than 98% is found.
Tetramethylammonium Hydroxide,
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Assay—
Accurately weigh a glass-stoppered flask containing about 15 mL of water. Add a quantity of a solution of tetramethylammonium hydroxide, equivalent to about 200 mg of (CH3)4NOH, and again weigh. Add methyl red TS, and titrate the solution with 0.1 N hydrochloric acid VS: each mL of 0.1 N hydrochloric acid is equivalent to 9.115 mg of (CH3)4NOH.
Residue on evaporation—
Evaporate 5 mL of solution on a steam bath, and dry at 105
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Ammonia and other amines—
Accurately weigh a quantity of solution, corresponding to about 300 mg of (CH3)4NOH, in a low-form weighing bottle tared with 5 mL of water. Add a slight excess of 1 N hydrochloric acid (about 4 mL), evaporate on a steam bath to dryness, and dry at 105
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Tetramethylammonium Hydroxide, Pentahydrate,
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Assay—
Accurately weigh about 800 mg, dissolve in 100 mL of water, and titrate with 0.1 N hydrochloric acid VS, determining the endpoint potentiometrically. Perform a blank determination, and make any necessary correction. Each mL of 0.1 N hydrochloric acid is equivalent to 18.22 mg of (CH3)4NOH·5H2O: not less than 98% is found.
Tetramethylammonium Hydroxide Solution in Methanol
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Assay—
Accurately weigh about 1 g of the solution, and dilute with water to about 50 mL. Add phenolphthalein TS, and titrate with 0.1 N hydrochloric acid VS to the disappearance of the pink color: each mL of 0.1 N hydrochloric acid VS is equivalent to 91.15 mg of (CH3)4NOH. Between 23% and 25% is found.
Clarity—
A portion of it in a test tube is clear, or only slightly turbid, when viewed transversely.
Tetramethylammonium Nitrate,
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Tetramethylbenzidine,
(4-(4-Amino-3,5-dimethylphenyl)-2,6-dimethylaniline; 3,3¢,5,5¢ Tetramethylbenzidine; 3,3¢5,5¢-Tetramethyl-[1,1¢-biphenyl] 4,4¢-diamine)
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4,4¢-Tetramethyldiaminodiphenylmethane
[(4,4¢-Methylenebis(N,N-dimethylaniline)],
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Melting range
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Tetramethylsilane,
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Tetrapropylammonium Chloride,
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Tetrasodium Ethylenediaminetetraacetate
((Ethylenedinitrilo)tetraacetic Acid Tetrasodium Salt),
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Loss on drying
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Thallous Chloride,
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Assay—
Dissolve about 500 mg, accurately weighed, in a mixture of 80 mL of water and 0.5 mL of sulfuric acid. When dissolution is complete, add 20 mL of hydrochloric acid. Heat to 60
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Theobromine,
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Assay—
Dissolve about 34 mg, accurately weighed, in 50 mL of glacial acetic acid. Titrate with 0.1 N perchloric acid VS, determining the endpoint potentiometrically. Perform a blank determination, and make any necessary correction. Each mL of 0.1 N perchloric acid is equivalent to 18.02 mg of C7H8N4O2. Not less than 95% is found.
Thiazole Yellow
(CI Direct Yellow 9; Clayton Yellow; Titan Yellow),
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Solubility—
A 200-mg portion mixed with 50 mL of water shows not more than a faint haze.
Residue on ignition—
Accurately weigh about 1.5 g, previously dried at 105
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Sensitiveness to magnesium—
Add 0.2 mL of a solution (1 in 10,000) and 2 mL of 1 N sodium hydroxide to a mixture of 9.5 mL of water and 0.5 mL of a solution prepared by dissolving 1.014 g of clear crystals of magnesium sulfate in water, diluting with water to 100 mL, then diluting 10 mL of the resulting solution with water to 1 L: a distinct pink color is produced within 10 minutes.
Thioacetamide,
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2-Thiobarbituric Acid,
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Melting temperature
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2,2¢-Thiodiethanol,
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Assay—
Not less than 98% of C4H10O2S is found, a suitable gas chromatograph equipped with a flame-ionization detector being used. The following conditions have been found suitable: a 4.0-mm × 1.83-m glass column is packed with 10% phase G25 on support S1A; the column, injection port, and detector temperatures are maintained at 200
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Refractive index
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Thioglycolic Acid,
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Sensitiveness—
Mix 1 mL with 2 mL of stronger ammonia water, and dilute with water to 20 mL. Add 1 mL of this solution to a mixture of 20 mL of water and 0.1 mL of dilute ferric chloride TS (1 in 100), then add 5 mL of ammonia TS: a distinct pink color is produced.
Thionine Acetate,
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Thiourea,
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Thorium Nitrate,
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Thrombin Human (Factor IIa )
— ~33,600
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Thromboplastin
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Loss on drying
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Thymidine,
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Thymol,
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Melting range
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Nonvolatile matter—
Volatilize 2 g on a steam bath, and dry at 105
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Thyroglobulin,
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Tin,
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Titanium Tetrachloride,
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Assay—
Accurately weigh 0.75 g into 100 mL of 2 N sulfuric acid contained in a Smith weighing buret. Pour the solution through a zinc–mercury reduction column into 50 mL of 0.1 N ferric ammonium sulfate VS. Elute with 100 mL of 2 N sulfuric acid and 100 mL of water. Add 10 mL of phosphoric acid, and titrate with 0.1 N potassium permanganate VS. Perform a blank determination, and make any necessary correction. Each mL of 0.1 N potassium permanganate is equivalent to 18.97 mg of TiCl4. Not less than 99.5% is found.
Boiling range (Reagent test):
between 135
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Titanium Trichloride
(Titanous Chloride),
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o-Tolidine
(4,4¢-Diamino-3,3¢-dimethylbiphenyl),
![]() ![]() ![]() ![]() Use a suitable grade with a content of NLT 98.0%.
Tolualdehyde
(o-Tolualdehyde),
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p-Tolualdehyde,
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Assay—
When examined by gas-liquid chromatography, it shows a purity of not less than 98%. The following conditions have been found suitable for assaying the article: A 3-mm × 1.8-m stainless steel column packed with a 5% phase G4 on support S1. Nitrogen, having a flow rate of about 12 mL per minute, is the carrier gas, the detector and column temperature are about 125
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Refractive index
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Toluene
(Toluol),
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p-Toluenesulfonic Acid,
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p-Toluenesulfonyl-l-arginine Methyl Ester Hydrochloride
(N
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p-Toluic Acid,
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Assay—
Transfer about 650 mg, accurately weighed, to a suitable container, dissolve in 125 mL of alcohol, add 25 mL of water, and mix. Titrate with 0.5 N sodium hydroxide VS, determining the endpoint potentiometrically. Perform a blank determination, and make any necessary correction. Each mL of 0.5 N sodium hydroxide is equivalent to 68.07 mg of C8H8O2: not less than 98% is found.
Melting range
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o-Toluidine
(2-Aminotoluene; 2-Methylaniline),
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Specific gravity
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Boiling range (Reagent test):
between 200
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p-Toluidine,
![]() ![]() ![]() ![]() Freely soluble in alcohol, in acetone, in methanol, and in dilute acids; slightly soluble in water.
Assay—
Dissolve 400 mg, accurately weighed, in 100 mL of glacial acetic acid, and titrate with 0.1 N perchloric acid VS, determining the endpoint potentiometrically. Perform a blank determination, and make any necessary correction. Each mL of 0.1 N perchloric acid is equivalent to 10.72 mg of CH3C6H4NH2. Not less than 98%, calculated on the dried basis, is found.
Loss on drying—
Weigh accurately about 1 g, and dry at 30
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Toluidine Blue,
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Toluidine Blue O,
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n-Triacontane,
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2,4,6-Triamino-5-nitrosopyrimidine,
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Assay—
Dissolve about 34 mg, accurately weighed, in 50 mL of glacial acetic acid. Titrate with 0.1 N perchloric acid VS, determining the endpoint potentiometrically. Perform a blank determination, and make any necessary corrections. Each mL of 0.1 N perchloric acid is equivalent to 15.41 mg of C4H6N6O. Not less than 97% is found.
Tributyl Phosphate
(Tri-n-butyl Phosphate),
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Refractive index
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Tributylethylammonium Hydroxide,
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Tributyrin
(Glyceryl Tributyrate),
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Assay—
Inject an appropriate specimen into a suitable gas chromatograph (see Chromatography
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Refractive index
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Acid content—
Transfer 1.0 g, accurately weighed, to a beaker, add 75 mL of methanol, and dissolve by stirring. When dissolution is complete, add 25 mL of water, and titrate with 0.05 N potassium hydroxide VS, using phenolphthalein TS as the indicator. Perform a blank determination, and make any necessary correction. Each mL of 0.05 N potassium hydroxide is equivalent to 88.1 mg of butyric acid: not more than 0.5% is found.
Trichloroacetic Acid,
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Trichlorofluoromethane,
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Assay—
Inject an appropriate specimen into a gas chromatograph (see Chromatography
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Refractive index
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Trichlorotrifluoroethane
—Use a suitable grade.
[Note—A suitable preparation, listed as “Freon-TF aerosol,” is available from E. I. du Pont de Nemours and Co., Wilmington, DE 19898. ]
n-Tricosane,
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Melting range
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Suitability—
Determine its suitability for use in the test for Related compounds under Propoxyphene Hydrochloride (USP monograph) as follows. Dissolve a suitable quantity in chloroform to yield a solution containing 20 µg per mL. Following the directions given in the test for Related compounds under Propoxyphene Hydrochloride, inject a suitable volume of the solution into the chromatograph, and record the chromatogram. Concomitantly record the chromatogram from the Standard preparation prepared as directed in the test for Related compounds: only one main peak is obtained from the n-tricosane solution, and no minor peaks are observed at, or near, the peak positions obtained for propoxyphene, acetoxy, or carbinol in the chromatogram from the Standard preparation.
Triethanolamine
—Use Trolamine (NF monograph).
Triethylamine,
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Triethylamine Hydrochloride,
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Assay—
Transfer about 35 mg, accurately weighed, to a suitable beaker, add 50 mL of glacial acetic acid, and dissolve by stirring. Add 5 mL of mercuric acetate TS, with stirring. When solution is complete, titrate with 0.1 N perchloric acid VS, determining the endpoint potentiometrically. Perform a blank titration, and make any necessary correction. Each mL of 0.1 N perchloric acid is equivalent to 13.77 mg of C6H15N·HCl. Not less than 97.5% of C6H15N·HCl is found.
Melting point
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Triethylamine Phosphate
(Triethylammonium Phosphate),
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[Note—A suitable grade is available from www. tciamerica.com, catalog number T1300. ]
Triethylene Glycol,
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Assay—
Inject an appropriate test specimen into a suitable gas chromatograph equipped with a flame-ionization detector (see Chromatography
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Refractive index
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Triethylenediamine
(1,4-Diazobicyclo[2.2.2]octane),
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Trifluoroacetic Acid,
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Assay—
Dissolve about 300 mg, accurately weighed, in 25 mL of water and 25 mL of alcohol. Titrate with 0.1 N sodium hydroxide VS, determining the endpoint potentiometrically. Perform a blank determination, and make any necessary corrections. Each mL of 0.1 N sodium hydroxide is equivalent to 11.40 mg of C2HF3O2. Not less than 99% is found.
Trifluoroacetic Anhydride,
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Assay—
Transfer about 0.8 g, accurately weighed, to a glass-stoppered flask containing 50 mL of methanol. Add 500 mg of phenolphthalein, and titrate with 0.1 N sodium methoxide VS to a pink endpoint. Calculate A by the formula:
V/W
in which V is the volume, in mL, of 0.1 N sodium methoxide and W is the weight, in mg, of test specimen. To a second glass-stoppered flask containing 50 mL of a mixture of dimethylformamide and water (1:1) transfer 0.4 g, accurately weighed, of the specimen under test, add 500 mg of phenolphthalein, and titrate with 0.1 N sodium hydroxide VS to a pink endpoint. Calculate B by the formula:
V1/W1
in which V1 is the volume, in mL, of 0.1 N sodium hydroxide and W1 is the weight, in mg, of test specimen. Calculate the percentage of (F3CCO)2O by the formula:
2100.3(B
Not less than 97% is found. If 2A is greater than B, calculate the percentage of F3CCOOH by the formula:
![]() 1140.3(2A
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Melting range
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2,2,2-Trifluoroethanol,
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Assay—
Inject an appropriate specimen into a gas chromatograph (see Chromatography
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Boiling range:
between 77
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2,2,2-Trifluoroethyldifluoromethyl Ether
(Difluoromethyl-2,2,2-trifluoroethyl ether),
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Boiling range:
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[Note—A suitable grade is available from PCR Incorporated, P.O. Box 1466, Gainesville, FL 32602. Tel: 904-376-8246. The catalogue number is 17151-2. ]
(m-Trifluoromethylphenyl) Trimethylammonium Hydroxide in Methanol
—Use a suitable grade.
[Note—A suitable grade is available as “Meth-Prep II” from Alltech, www.alltechweb.com. ]
5-(Trifluoromethyl)uracil,
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Assay—
When tested by thin-layer chromatography, with the use of plates coated with chromatographic silica gel mixture, a developing system consisting of chloroform, methanol, and acetic acid (17:2:1), and examined visually and under long-wavelength UV light, a single spot is exhibited.
Trifluorovinyl Chloride Polymer (Fluorolube; 1-Chloro-1,2,2-trifluoro-ethene Homopolymer),
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[Note—A suitable grade is available as catalog number Z123552 from www.sigma-aldrich.com. ]
Trimethylacethydrazide Ammonium Chloride
(Betaine Hydrazide Chloride; Girard Reagent T),
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Melting range
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Residue on ignition (Reagent test)—
Ignite 1 g with 0.5 mL of sulfuric acid: the residue weighs not more than 10 mg (1%).
2,2,4-Trimethylpentane
(Isooctane),
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2,4,6-Trimethylpyridine
(5-Collidine),
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Assay—
Inject an appropriate test specimen into a suitable gas chromatograph (see Chromatography
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Refractive index
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N-(Trimethylsilyl)-imidazole,
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Refractive index
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Trimethyltin Bromide,
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2,4,6-Trinitrobenzenesulfonic Acid,
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Trioctylphosphine Oxide,
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Melting range
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1,3,5-Triphenylbenzene,
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Melting range
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Triphenylmethane,
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Assay—
Inject an appropriate volume into a gas chromatograph (see Chromatography
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Melting range
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Triphenylmethanol,
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Assay—
Inject an appropriate volume into a gas chromatograph (see Chromatography
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Triphenyltetrazolium Chloride,
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Solubility—
Separate 100-mg portions dissolve completely in 10 mL of water and in 10 mL of alcohol, respectively, to yield solutions that are clear, or practically so.
Loss on drying
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Residue on ignition (Reagent test):
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Sensitiveness—
Dissolve 10 mg in 10 mL of dehydrated alcohol (A). Then dissolve 10 mg of dextrose in 20 mL of dehydrated alcohol (B). To 0.2 mL of B add 1 mL of dehydrated alcohol and 0.5 mL of dilute tetramethylammonium hydroxide TS (1 volume diluted with 9 volumes of dehydrated alcohol), then add 0.2 mL of A: a pronounced red color develops within about 10 minutes.
Tris(2-aminoethyl)amine,
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Assay—
Dissolve about 80 mg in 30 mL of methanol. Add 40 mL of water, and titrate with 1 N hydrochloric acid, determining the endpoint potentiometrically. Perform a blank determination, and make any necessary correction. Each mL of 1 N hydrochloric acid is equivalent to 48.75 mg of C6H18N4. Not less than 98.0% is found.
Refractive index
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Tris(hydroxymethyl)aminomethane
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Tris(hydroxymethyl)aminomethane Acetate,
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Tris(hydroxymethyl)aminomethane Hydrochloride,
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N-Tris(hydroxymethyl)methylglycine,
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Tritirachium Album Proteinase K—
Use a suitable grade.
[Note—A suitable grade can be obtained from Qiagen, Inc., www.qiagen.com. ]
Tromethamine
[Tris(hydroxymethyl)aminomethane; THAM; 2-Amino-2-(hydroxymethyl)-1,3-propanediol],
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Tropaeolin OO
(Acid Orange 5),
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pH range:
from 1.4 (red) to 2.6 (yellow).
Tropic Acid,
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Tropine,
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Trypan Blue
(Direct Blue 14),
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l-Tryptophane,
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Assay—
Accurately weigh about 300 mg, dissolve in a mixture of 3 mL of formic acid and 50 mL of glacial acetic acid, add 2 drops of crystal violet TS, and titrate with 0.1 N perchloric acid VS to a green endpoint. Each mL of 0.1 N perchloric acid is equivalent to 20.42 mg of C11H12N2O2. Between 98.0% and 102.0%, calculated on the dried basis, is found.
Specific rotation
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Loss on drying
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Residue on ignition (Reagent test):
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Tyrosine—
Dissolve 100 mg in 3 mL of diluted sulfuric acid, add 10 mL of mercuric sulfate TS, and heat on a steam bath for 10 minutes. Filter, wash with 5 mL of mercuric sulfate TS, and add to the combined filtrate 0.5 mL of sodium nitrite solution (1 in 20): no red color is produced within 15 minutes.
Tuberculin, Purified Protein Derivative (Tuberculin PPD)—
Derived from the human strain of Mycobacterium tuberculosis, and available either as a solution or as a lyophilized powder. For lyophilized powder, reconstitute according to the manufacturer's instructions using the diluent provided by the manufacturer. Solutions may contain a stabilizer and a preservative. One Tuberculin Unit (TU) is equivalent to 0.02 µg of Tuberculin PPD.
Tubocurarine Chloride (7¢,12¢-Dihydroxy-6,6¢-dimethoxy-2,2¢,2¢-trimethyltubocuraranium Chloride),
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[Note—A suitable grade is available from Acros Organics, catalog number 24349 at www.acros.com. ]
Tungstic Acid,
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l-Tyrosine Disodium,
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Auxiliary Information—
Please check for your question in the FAQs before contacting USP.
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