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Merck

1602003

USP

Resorcinol

United States Pharmacopeia (USP) Reference Standard

Synonym(s):

1,3-Benzenediol

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About This Item

Linear Formula:
C6H4-1,3-(OH)2
CAS Number:
108-46-3
Molecular Weight:
110.11
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329751037
MDL number:
MFCD00002269
Beilstein/REAXYS Number:
906905

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InChI

1S/C6H6O2/c7-5-2-1-3-6(8)4-5/h1-4,7-8H

SMILES string

Oc1cccc(O)c1

InChI key

GHMLBKRAJCXXBS-UHFFFAOYSA-N

grade

pharmaceutical primary standard

vapor density

3.8 (vs air)

vapor pressure

1 mmHg ( 21.1 °C)

API family

resorcinol

autoignition temp.

1126 °F

manufacturer/tradename

USP

bp

178 °C/16 mmHg (lit.)

mp

109-112 °C (lit.)

application(s)

pharmaceutical (small molecule)

format

neat

storage temp.

2-8°C

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1 of 4

This Item
16101533631.07590
Resorcinol United States Pharmacopeia (USP) Reference Standard

USP

1602003

Resorcinol

Resorcinol meets analytical specification of Ph. Eur., BP, 98.5-100.5% (calc. to the dried substance)

Sigma-Aldrich

16101

Resorcinol

Resorcinol certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

Supelco

53363

Resorcinol

Resorcinol extra pure

SAFC

1.07590

Resorcinol

manufacturer/tradename

USP

manufacturer/tradename

-

manufacturer/tradename

Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

manufacturer/tradename

-

grade

pharmaceutical primary standard

grade

-

grade

certified reference material, TraceCERT®

grade

-

application(s)

pharmaceutical (small molecule)

application(s)

pharmaceutical (small molecule)

application(s)

cleaning products
cosmetics
environmental
food and beverages
personal care

application(s)

pharma/biopharma processes

format

neat

format

-

format

neat

format

-

vapor density

3.8 (vs air)

vapor density

3.8 (vs air)

vapor density

3.8 (vs air)

vapor density

-

vapor pressure

1 mmHg ( 21.1 °C)

vapor pressure

1 mmHg ( 21.1 °C)

vapor pressure

1 mmHg ( 21.1 °C)

vapor pressure

0.1 hPa ( 20 °C)

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

Resorcinol USP reference standard, intended for use in specified quality tests and assays as specified in the USP compendia. Also, for use with USP monographs such as:
  • Fluorescein Injection
  • Fluorescein Sodium
  • Resorcinol
  • Resorcinol and Sulfur Topical Suspension

Analysis Note

These products are for test and assay use only. They are not meant for administration to humans or animals and cannot be used to diagnose, treat, or cure diseases of any kind.  ​

Other Notes

Sales restrictions may apply.

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Pricing

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 3 - Eye Dam. 1 - Skin Irrit. 2 - Skin Sens. 1B - STOT SE 1 Oral - STOT SE 2 Oral

target_organs

Central nervous system,Blood, Respiratory system

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

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Claudio B S Oliveira et al.
Molecules (Basel, Switzerland), 19(5), 5898-5912 (2014-05-09)
A resorcinarene derivative of vanillin, resvan, was synthesized and characterized by spectroscopic techniques. We measured the cytotoxicity (in vivo and in vitro), antioxidant and anti-Toxoplasma activities of vanillin and the resorcinarene compound. Here we show that vanillin has a dose-dependent
Valerio Chiurchiù et al.
International immunology, 27(3), 153-160 (2014-10-27)
G protein-coupled receptor 55 (GPR55) is activated by endogenous, plant-derived and synthetic cannabinoids. Recent studies reported a broad tissue distribution for GPR55 and found prominent roles for this receptor in inflammatory pain, gut and bone physiology, as well as cancer.
M N Kardar et al.
Phytochemistry, 106, 156-163 (2014-08-12)
Chemical investigation of a sample of propolis originating from North-Western Cameroon led to the isolation of thirteen alk(en)ylphenols (1-13) (inseparable mixture) along with α-amyrin (14), β-amyrin (15), lupeol (16), cycloartenol (17), mangiferonic acid (18), ambonic acid (19), mangiferolic acid (20)
Sebastian Weis et al.
Pancreas, 43(8), 1277-1285 (2014-08-08)
The gene p8 was initially described in pancreatic tissue during acute experimental pancreatitis, a disease that is characterized by a systemic immune response. Although early reports suggested that p8 affects leukocyte migration during acute pancreatitis (AP), no studies revealing its
Linlin Qi et al.
Analytical and bioanalytical chemistry, 407(13), 3617-3625 (2015-03-23)
An aqueous two-phase microfluidics (ATPM) method suitable for selective extraction of bisphenol A (BPA) in aqueous samples was developed, and a functional ionic liquid of N, N, N-trioctyl ammonium propionate (TOAP) was specially employed for the formation of a parallel
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