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Merck

PHR1582

Dehydroacetic acid

Pharmaceutical Secondary Standard; Certified Reference Material

Synonyme(s) :

Dehydroacetic acid, 2-Acetyl-5-hydroxy-3-oxo-4-hexenoic acid δ-lactone

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A propos de cet article

Formule empirique (notation de Hill) :
C8H8O4
Numéro CAS:
Poids moléculaire :
168.15
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
208-293-9
Beilstein/REAXYS Number:
6129
MDL number:
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Nom du produit

Dehydroacetic acid, Pharmaceutical Secondary Standard; Certified Reference Material

Quality Level

InChI key

PGRHXDWITVMQBC-UHFFFAOYSA-N

InChI

1S/C8H8O4/c1-4-3-6(10)7(5(2)9)8(11)12-4/h3,7H,1-2H3

SMILES string

CC(=O)C1C(=O)OC(C)=CC1=O

grade

certified reference material
pharmaceutical secondary standard

agency

traceable to USP 1166309

API family

dehydroacetic acid

CofA

current certificate can be downloaded

packaging

pkg of 1 g

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

270 °C (lit.)

mp

111-113 °C (lit.)

application(s)

pharmaceutical (small molecule)

format

neat

storage temp.

2-30°C

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Analysis Note

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

Application

Dehydroacetic acid may be used as a pharmaceutical reference standard for the determination of the analyte in pharmaceutical, food and cosmetic formulations by chromatography.
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.

General description

Dehydroacetic acid is a pyrone derivative, that is typically synthesized by the base-catalyzed dimerization of diketene. It is used as a preservative in pharmaceutical, food and cosmetic products.
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.

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.
To see an example of a Certificate of Analysis for this material enter LRAA4498 in the slot below. This is an example certificate only and may not be the lot that you receive.

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

Classe de stockage

13 - Non Combustible Solids

wgk

WGK 1

flash_point_f

314.6 °F

flash_point_c

157 °C


Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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Consulter la Bibliothèque de documents

Simultaneous determination of sorbic acid, dehydroacetic acid and benzoic acid by gas chromatography-mass spectrometry
Kakemoto M
Journal of Chromatography A, 594(1-2), 253-257 (1992)
Dehydroacetic acid, triacetic acid lactone, and related pyrones
Advances in Heterocyclic Chemistry, 53, 1-84 (1992)
Simultaneous determination of nine kinds of preservatives in foods by HPLC
Kishi H and Yamada T
Journal of Food Hygiene and Safety, 48(3), 58-63 (2007)
Comparing micellar electrokinetic chromatography and microemulsion electrokinetic chromatography for the analysis of preservatives in pharmaceutical and cosmetic products
Huang HY, et al.
Journal of Chromatography A, 993(1-2), 153-164 (2003)
E Mikami et al.
Journal of pharmaceutical and biomedical analysis, 28(2), 261-267 (2002-04-04)
A high-performance liquid chromatographic (HPLC) method for simultaneous determination of dehydroacetic acid (DHA), benzoic acid (BA), sorbic acid (SOA) and salicylic acid (SA) was developed for application to cosmetic products. Isocratic reversed-phase HPLC was employed for quantitative analysis using tetra-n-butylammonium

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