PHR1022
Butylparaben
Pharmaceutical Secondary Standard; Certified Reference Material
Synonym(s):
4-Hydroxybenzoic acid butyl ester
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About This Item
Empirical Formula (Hill Notation):
C11H14O3
CAS Number:
Molecular Weight:
194.23
Beilstein:
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.
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Product No.
Description
Pricing
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Skin Irrit. 2
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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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)
Anna Viridén et al.
European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 77(1), 99-110 (2010-11-18)
This study investigates the effect of the chemical heterogeneity of hydroxypropyl methylcellulose (HPMC) on the release of model drug substances from hydrophilic matrix tablets. The hypothesis was that the release of drug substances could be influenced by possible interactions with
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