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1602003

USP

Resorcinol

United States Pharmacopeia (USP) Reference Standard

Synonim(y):

1,3-Benzenediol

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Gabaryty przesyłkiSKUDostępnośćCena netto
200 mg
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1910,00 zł

Informacje o tej pozycji

Wzór liniowy:
C6H4-1,3-(OH)2
Numer CAS:
Masa cząsteczkowa:
110.11
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
906905

1910,00 zł


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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

SMILES string

Oc1cccc(O)c1

InChI

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

InChI key

GHMLBKRAJCXXBS-UHFFFAOYSA-N

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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Ta pozycja
Y0000767PHR120116101
Resorcinol United States Pharmacopeia (USP) Reference Standard

USP

1602003

Resorcinol

Resorcinol European Pharmacopoeia (EP) Reference Standard

Y0000767

Resorcinol

grade

pharmaceutical primary standard

grade

pharmaceutical primary standard

grade

certified reference material, pharmaceutical secondary standard

grade

-

manufacturer/tradename

USP

manufacturer/tradename

EDQM

manufacturer/tradename

-

manufacturer/tradename

-

application(s)

pharmaceutical (small molecule)

application(s)

pharmaceutical (small molecule)

application(s)

pharmaceutical (small molecule)

application(s)

pharmaceutical (small molecule)

format

neat

format

neat

format

neat

format

-

autoignition temp.

1126 °F

autoignition temp.

1126 °F

autoignition temp.

1126 °F

autoignition temp.

1126 °F

mp

109-112 °C (lit.)

mp

109-112 °C (lit.)

mp

109-112 °C (lit.)

mp

109-112 °C (lit.)


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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

Klasa składowania

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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Certyfikaty analizy (CoA)

Lot/Batch Number

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Masz już ten produkt?

Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów



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
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



Numer pozycji handlu globalnego

SKUNUMER GTIN
1602003-200MG04061838745323

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