1524806
USP
Phenol
United States Pharmacopeia (USP) Reference Standard
Synonym(s):
Hydroxybenzene
About This Item
Recommended Products
grade
pharmaceutical primary standard
vapor density
3.24 (vs air)
vapor pressure
0.09 psi ( 55 °C)
0.36 mmHg ( 20 °C)
API family
salicylic acid, guaiacol, hexylresorcinol
autoignition temp.
1319 °F
expl. lim.
8.6 %
manufacturer/tradename
USP
bp
182 °C (lit.)
mp
40-42 °C (lit.)
density
1.071 g/mL at 25 °C (lit.)
application(s)
pharmaceutical (small molecule)
format
neat
storage temp.
2-8°C
SMILES string
Oc1ccccc1
InChI
1S/C6H6O/c7-6-4-2-1-3-5-6/h1-5,7H
InChI key
ISWSIDIOOBJBQZ-UHFFFAOYSA-N
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General description
This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets, have been developed and issued under the Authority of the issuing Pharmacopoeia. For further information and support please go to the website of the issuing Pharmacopoeia.
Application
Also used to prepare standard stock, standard, Peak identification, and system suitability solution during the assay and impurity analysis by using liquid and gas chromatography in conjunction with UV and Flame ionization detectors according to the below monographs of united states pharmacopeia (USP) :
- Camphorated Phenol Topical Gel
- Salicylic Acid
- Magnesium Salicylate
- Sodium Salicylate
Analysis Note
Other Notes
related product
signalword
Danger
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Muta. 2 - Skin Corr. 1B - STOT RE 2
Storage Class
6.1A - Combustible, acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk_germany
WGK 2
flash_point_f
177.8 °F - closed cup
flash_point_c
81 °C - closed cup
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Protocols
Under applied conditions, system suitability criteria are met, and the Chloroquine Phosphate HPLC Assay and Impurity Profiling Methods demonstrate good resolution/selectivity, reproducibility, and sensitivity.
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