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1577008

USP

Propylparaben

Name: Propylparaben
Brand: USP

United States Pharmacopeia (USP) Reference Standard

Synonym(s):

Propyl 4-hydroxybenzoate, 4-Hydroxybenzoic acid propyl ester, Propyl paraben

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About This Item

Linear Formula:

HOC₆H₄CO₂CH₂CH₂CH₃

CAS Number:

94-13-3

Molecular Weight:

180.20

UNSPSC Code:

41116107

NACRES:

NA.24

PubChem Substance ID:

329750996

MDL number:

MFCD00002354

Beilstein/REAXYS Number:

1103245

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Properties

grade

pharmaceutical primary standard

API family

parabens

manufacturer/tradename

USP

mp

95-98 °C (lit.)

application(s)

pharmaceutical (small molecule)

format

neat

SMILES string

CCCOC(=O)c1ccc(O)cc1

InChI

1S/C10H12O3/c1-2-7-13-10(12)8-3-5-9(11)6-4-8/h3-6,11H,2,7H2,1H3

InChI key

QELSKZZBTMNZEB-UHFFFAOYSA-N

Description

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

Propylparaben 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:

Propylparaben Sodium
Bacteriostatic Sodium Chloride Injection
Chlorambucil Tablets
Dexamethasone Oral Solution
Aripiprazole Tablets
Butylparaben

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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hcodes

H412

pcodes

P273 - P501

Hazard Classifications

Aquatic Chronic 3

Storage Class

11 - Combustible Solids

flash_point_f

356.0 °F

flash_point_c

180 °C

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Pharmacokinetics of loxoprofen and its active metabolite after dermal application of loxoprofen gel to rats.

R Sawamura et al.

Die Pharmazie, 70(2), 74-80 (2015-05-23)

This study was conducted to evaluate the pharmacokinetics of loxoprofen (LX) and its active metabolite (trans-OH form) after a single dermal application of LX gel (LX-G) to rats. In the skin at the treated site, generation of the trans-OH form

Actions of methyl-, propyl- and butylparaben on estrogen receptor-α and -β and the progesterone receptor in MCF-7 cancer cells and non-cancerous MCF-10A cells.

Anna Maria Wróbel et al.

Toxicology letters, 230(3), 375-381 (2014-08-17)

Numerous studies have shown that widely used parabens possess estrogenic properties. In the present study, we examined the effects of methyl-, propyl- and butylparaben on the mRNA and protein expression of estrogen receptor (ER)-α (ESR1) and -β (ESR2) and the

Use of topical liposomes containing meglumine antimoniate (Glucantime) for the treatment of L. major lesion in BALB/c mice.

S A Moosavian Kalat et al.

Experimental parasitology, 143, 5-10 (2014-05-02)

Treatment of cutaneous leishmaniasis (CL) is a dream for the patients, health care authorities and scientists. The aim of this study was to develop a topical liposomal meglumine antimoniate (MA, Glucantime™) (Lip-MA) formulation and evaluate the therapeutic effects of the

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Global Trade Item Number

SKU	GTIN
1577008-200MG	04061838743510