Skip to Content
Merck
CN

30750

Dehydroacetic acid sodium salt

≥98.0% (NT)

Synonym(s):

2-Acetyl-5-hydroxy-3-oxo-4-hexenoic acid δ-lactone sodium salt

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Empirical Formula (Hill Notation):
C8H7NaO4
CAS Number:
Molecular Weight:
190.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
224-580-1
Beilstein/REAXYS Number:
4893653
MDL number:
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist


assay

≥98.0% (NT)

mp

~295 °C (dec.)

SMILES string

[Na+].CC(=O)C1=C([O-])C=C(C)OC1=O

InChI

1S/C8H8O4.Na/c1-4-3-6(10)7(5(2)9)8(11)12-4;/h3,10H,1-2H3;/q;+1/p-1

InChI key

ZPNRBQVNNIDJHX-UHFFFAOYSA-M

General description

The kinetics of dehydroacetic acid sodium salt decomposition, in presence of formaldehyde and formaldehyde donors, was studied.

Application

Dehydroacetic acid sodium salt was used as a model preservative to study the relevant kinetic and formulation parameters of the device intended for the prolonged release of antimicrobial agents.


Still not finding the right product?

Explore all of our products under Dehydroacetic acid sodium salt


pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

13 - Non Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves



Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library



A Gazzaniga et al.
International journal of cosmetic science, 16(3), 105-112 (1994-06-01)
Synopsis The kinetics of decomposition of the sodium salt of dehydroacetic acid (DHA.Na) in presence of formaldehyde and formaldehyde donors was investigated. The possibility of preparing systems capable of providing the cosmetic preparation with increasing amounts of DHA.Na corresponding to
Allergic contact dermatitis caused by sodium dehydroacetate, not hyaluronic acid, in Ialuset® cream.
Brigitte Milpied et al.
Contact dermatitis, 65(6), 359-361 (2011-11-15)
Luiz C Dias et al.
Journal of agricultural and food chemistry, 57(4), 1399-1405 (2009-01-28)
A short and efficient approach to a range of new chiral and achiral functionalized (E)-enaminopyran-2,4-diones starting with commercially available dehydroacetic acid is described. The phytotoxic properties of these (E)-enaminopyran-2,4-diones were evaluated by their ability to interfere with the growth of