Molecular Formula | C10H12O3 |
Molar Mass | 180.2 |
Density | 1.134g/cm3 |
Melting Point | 95-99℃ |
Boling Point | 294.3°C at 760 mmHg |
Flash Point | 124.6°C |
Water Solubility | <0.1 g/100 mL at 12℃ |
Solubility | Soluble in ethanol, ether, acetone and other organic solvents, slightly soluble in water. |
Vapor Presure | 0.00093mmHg at 25°C |
Appearance | White crystalline powder |
Storage Condition | 2-8℃ |
Refractive Index | 1.531 |
MDL | MFCD00002354 |
Physical and Chemical Properties | Character: white crystal, with special odor. Propyl p-carboxybenzoate is colorless fine crystal or white crystalline powder, almost odorless, slightly astringent soluble in ethanol, ether, acetone and other organic solvents, slightly soluble in water. |
Use | As a bacteriostatic preservative in pharmaceuticals, cosmetics |
Safety Description | S24/25 - Avoid contact with skin and eyes. |
colorless fine crystal or white crystalline powder, almost odorless, slightly astringent. The melting point was 95-98 °c. Soluble in 2000 water, soluble in ethanol (95g/lOOmL), propylene glycol (26g/lOOmL) and acetone (105g/lOOmL) and other organic solvents.
from p-Hydroxybenzoic acid and N-propanol esterification, decolorization, recrystallization.
This product is propyl 4-hydroxybenzoate. Calculated as dry product, including C1()H1203 should be 98.0% ~ 102.0%.
The melting point of this product (General 0612) is 96 ~ 99C.
preservative. See ethyl paraben for others.
Take 2ml of solution under the items of clarity and color, add 2M l of ethanol and 5ml of water, shake well, add 2 drops of bromocresol green indicator solution, and use sodium hydroxide titration solution (0. lm o l/L) titration to blue, consumption of sodium hydroxide titration solution (0. lm o l/L) must not pass 0. lm l.
take this product l.O g, after dissolving with 0901 of ethanol, check according to law (general rule and General Rule 0 9 0 2 ) , the solution should be clear and colorless, it shall not be deeper than the yellow or yellow-green standard colorimetric solution No. 1 (General rule 0901 method 1).
take this product 2 .0g, add 50ml of water, 80X: water bath heating for 5 minutes, let cool, filter, take filtrate 5 .0M l, checked by law (General rule 0801), must not be more concentrated (0.035%) than the control solution made of standard sodium chloride solution.
take 25ml of filtrate under chloride item, check according to law (General Rule 0 8 0 2 ) , and standard potassium sulfate solution 2. Compared with the control solution made of 4m l, it should not be more concentrated (0. 024%).
take this product, add the mobile phase to dissolve and dilute the solution containing lm g per lm l as the test solution; Take lm l with precision and put it in a 100ml measuring flask, the mobile phase was diluted to the scale, and the solution was used as a control solution. According to the chromatographic conditions under the content determination item, take 20M1 of the control solution and inject it into the human liquid chromatograph to adjust the detection sensitivity so that the peak height of the main component peak is about 25% of the full scale, then 20ul of the test solution and the control solution are accurately measured, and the human liquid chromatograph is injected respectively, and the chromatogram is recorded to 4 times of the retention time of the main peak. If the impurity peak is shown in the chromatogram of the test solution, the area of the single impurity peak shall not be greater than 0 of the area of the main peak of the control solution. 4 times (0 .4% ), the sum of each impurity peak area shall not be greater than 0. 8 times (0. 8%).
take this product, put it in a silica gel dryer, and dry it under reduced pressure to constant weight. The weight loss shall not exceed 0831 (general rule).
The l.O g of this product shall be taken for inspection according to law (General rule 0841), and the remaining residue shall not exceed.
The residue left under the ignition residue item shall not contain more than 20 parts per million of heavy metals as determined by law (general chapter 0821 second method).
take this product l.0g, add calcium hydroxide l.O g, mix, add a small amount of water, stir evenly, dry, first burn with small fire to charring, then burn at 500 ~ 600TC to completely Ash, cool, add hydrochloric acid (5m) and water (23ml), check according to law (General Principles 0822 The first law), should comply with the provisions (0.0002%).
measured by high performance liquid chromatography (General 0512).
pharmaceutical excipients, bacteriostatic agents.
sealed storage.