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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:
Form:
powder
InChI key
ZPNRBQVNNIDJHX-UHFFFAOYSA-M
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
SMILES string
[Na+].CC(=O)C1=C([O-])C=C(C)OC1=O
form
powder
quality
Arxada quality
manufacturer/tradename
Arxada AG
concentration
99.0-100.3 % (w/w) (T)
impurities
≤0.5 % (w/w) water (Karl Fischer)
mp
~295 °C (dec.)
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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B S Lao et al.
Se pu = Chinese journal of chromatography, 19(2), 137-140 (2003-01-25)
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The reaction between o-phenylenediamines, dehydroacetic acid and aromatic aldehydes is shown to give not only the expected 1,5-benzodiazepine derivative but also a 3,4-dihydroquinoxaline, the structure of which was determined by its 1H and 13C 1D and 2D NMR spectra.
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HPLC method of determination of dehydroacetic acid and its sodium salt in food products and polymeric packing materials has been developed. The migration of DGA from food-contacting materials to food matrix has been investigated.
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A high-performance liquid chromatography (HPLC) method was developed to determine dehydroacetic acid (DHA) residues in chicken muscle, liver and kidney. DHA was extracted using acetonitrile, and clean-up performed using a strong anion exchange (PAX) SPE column. The cleaned-up samples were
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