W390003
Sodium diacetate
Synonym(s):
Sodium hydrogen diacetate
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About This Item
Empirical Formula (Hill Notation):
C4H7NaO4
CAS Number:
Molecular Weight:
142.09
FEMA Number:
3900
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
16.073
EC Number:
204-814-9
NACRES:
NA.21
MDL number:
Organoleptic:
faint
Biological source:
synthetic
Food allergen:
no known allergens
SMILES string
[Na+].CC(O)=O.CC([O-])=O
InChI
1S/2C2H4O2.Na/c2*1-2(3)4;/h2*1H3,(H,3,4);/q;;+1/p-1
InChI key
BHZOKUMUHVTPBX-UHFFFAOYSA-M
biological source
synthetic
reg. compliance
FCC, FDA 21 CFR 184.1754
form
solid
mp
323-329 °C (lit.)
application(s)
flavors and fragrances
documentation
see Safety & Documentation for available documents
food allergen
no known allergens
organoleptic
faint
Quality Level
General description
Sodium diacetate is a flavoring compound that is also used as an anti-microbial agent for meat products.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1
Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Dictionary of Food Compounds with CD-ROM: Additives, Flavors, and Ingredients, 1729-1729 null
Modeling the growth of Listeria monocytogenes in cured ready-to-eat processed meat products by manipulation of sodium chloride, sodium diacetate, potassium lactate, and product moisture content.
Seman DL, et al.
Journal of Food Protection, 65(4), 651-658 (2002)
Michael P Gotsbacher et al.
Chembiochem : a European journal of chemical biology, 21(10), 1433-1445 (2019-12-22)
This work aimed to undertake the in situ conversion of the terminal amine groups of bacterial desferrioxamine (DFO) siderophores, including desferrioxamine B (DFOB), to azide groups to enable downstream click chemistry. Initial studies trialed a precursor-directed biosynthesis (PDB) approach. Supplementing Streptomyces
Huiling Zhu et al.
Molecular nutrition & food research, 62(9), e1700814-e1700814 (2018-03-07)
Flaxseed oil is a rich source of α-linolenic acid (ALA), which is the precursor of the long-chain n-3 polyunsaturated fatty acids (PUFAs), including docosahexaenoic acid (DHA) and eicosapentaenoic acid (EPA). This study investigates the protective effect of flaxseed oil against
Albert N Ngo et al.
Pharmaceutical research, 33(2), 367-383 (2015-11-11)
It is hypothesized that sodium acetate (SA) can be used for in situ coating of drug loaded chitosan NPs for improved physico-chemical properties. Tenofovir (TFV) is used as a model drug. Uncoated chitosan NPs are prepared by ionic gelation. SA
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