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Merck

PHR1022

Supelco

Butylparaben

Pharmaceutical Secondary Standard; Certified Reference Material

Sinónimos:

4-Hydroxybenzoic acid butyl ester

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About This Item

Fórmula empírica (notación de Hill):
C11H14O3
Número de CAS:
Peso molecular:
194.23
Beilstein/REAXYS Number:
1103741
EC Number:
MDL number:
UNSPSC Code:
41116107
NACRES:
NA.24

grade

certified reference material
pharmaceutical secondary standard

Quality Level

agency

traceable to Ph. Eur. B1217000
traceable to USP 1084000

API family

parabens

CofA

current certificate can be downloaded

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care
pharmaceutical (small molecule)

format

neat

storage temp.

2-30°C

InChI

1S/C11H14O3/c1-2-3-8-14-11(13)9-4-6-10(12)7-5-9/h4-7,12H,2-3,8H2,1H3

InChI key

QFOHBWFCKVYLES-UHFFFAOYSA-N

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General description

Butylparaben is a compound, which belongs to the class of parabens.
Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards.

Application

Butylparaben may be used as a reference standard for the determination of the analyte in cosmetics, food samples and human breast cancerous tissue by chromatography techniques.
Butylparaben may be used as an internal standard in the analysis of aspirin and warfarin in pharmaceutical formulations using reversed-phase high performance liquid chromatography (RP-HPLC).
These Secondary Standards are qualified as Certified Reference Materials. These are suitable for use in several analytical applications including but not limited to pharma release testing, pharma method development for qualitative and quantitative analyses, food and beverage quality control testing, and other calibration requirements.

Analysis Note

These secondary standards offer multi-traceability to the USP, EP (PhEur) and BP primary standards, where they are available.

Other Notes

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

Footnote

To see an example of a Certificate of Analysis for this material enter LRAB7759 in the slot below. This is an example certificate only and may not be the lot that you receive.

Recommended products

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Eye Dam. 1 - Skin Irrit. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


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Visite la Librería de documentos

Evaluation of PGC Stationary Phases Under High-Temperature LC Conditions for the Analysis of Parabens in Food Samples
La Tella R, et al.
LC-GC, 36(5), 8-8 (2023)
Development and validation of a reversed-phase liquid chromatographic method for analysis of aspirin and warfarin in a combination tablet formulation
Montgomery RE, et al.
Journal of Pharmaceutical and Biomedical Analysis, 15, 73-82 (1996)
Effects of butylparaben on the male reproductive system in rats
Oishi S
Toxicology and Industrial Health, 17, 31-39 (2001)
GC-MS method for the determination of paraben preservatives in the human breast cancerous tissue.
Shanmugam G, et al.
Microchemical Journal, Devoted to the Application of Microtechniques in All Branches of Science, 96(2), 391-396 (2010)
A Beltran et al.
Analytica chimica acta, 677(1), 72-78 (2010-09-21)
In this paper we describe the synthesis, characterisation and use of two distinct molecularly imprinted polymers (MIPs) prepared using esters of p-hydroxybenzoic acid (parabens) as templates: one MIP was synthesised by precipitation polymerisation using a semi-covalent molecularly imprinting strategy with

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