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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Toxicological information

Direct observations: clinical cases, poisoning incidents and other

Administrative data

direct observations: clinical cases, poisoning incidents and other
Type of information:
other: data on putative metabolite
Adequacy of study:
supporting study
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Non GLP, non-guideline, human experimental study, published in peer reviewed literature, minor restrictions in design but otherwise adequate for assessment.

Data source

Reference Type:
Sodium acetate induces a metabolic alkalosis but not the increase in fatty acid oxidation observed following bicarbonate ingestion in humans
Smith GI, Jeukendrup AE and Ball D
Bibliographic source:
J. Nutr. 137:1750-1756

Materials and methods

Study type:
study with volunteers
Endpoint addressed:
basic toxicokinetics
Test guideline
no guideline followed
Principles of method if other than guideline:
The rate of oxidation of exogenous acetate was determined in human volunteers.
GLP compliance:
not specified

Test material

Constituent 1
Chemical structure
Reference substance name:
Sodium acetate
EC Number:
EC Name:
Sodium acetate
Cas Number:
Molecular formula:
sodium acetate
Details on test material:
- Name of test materials (as cited in study report):
Sodium acetate / NaAc (trihydrate)
- Physical state: not reported
- Analytical purity: not reported
- Impurities (identity and concentrations): not reported
- Lot/batch No.: not reported
- Radiochemical purity (if radiolabelling): not reported
- 13C labelling: 2 mg[1,2-13C]NaAc/kg bw added to NaAc drink giving enrichments of 707.6±69.2d/1000 vs. PDB determined by elemental analyser-isotope ratio mass spectrophotometry. NaH13CO3 at 0.064 mg/kg bw was infused immediately before drinking NaAc to prime the bicarbonate pool.


Type of population:
- Number of subjects exposed: 8
- Sex: 6 male and 2 female
- Age: 29±3 years
- Height: 1.76±0.03 m
- Body weight: 71.62±5.29 kg
- Known diseases: none (healthy volunteers)
Ethical approval:
confirmed and informed consent free of coercion received
Route of exposure:
other: oral: Sodium acetate... (see attached file)
Reason of exposure:
Exposure assessment:
Details on exposure:
In a randomised, crossover, single-blind experiment, on two occasions, at least 1 week apart, each volunteer drank 500 mL low-energy cordial (42 kJ/500 mL; 2.5 g carbohydrate/500 mL) which contained either NaAc (trihydrate) or NaHCo3 at 2 mmol/kg bw. The volunteers rested for at least 1 hour prior to drinking. The volunteers minimised 13C glycogen stores by at least 1 hour intense exercise 5 days prior to each visit. Volunteers' dietary intake was identical for each 5 day period prior to each experiment. During the experiment, volunteers avoided eating food derived from carbohydrates from C4 plants. Volunteers fasted overnight prior to experiment and drank 500 mL tap water prior to experiments.
-collection times: 2 consecutive pre-ingestion respiratory gas samples collected followed by samples every 30 minutes for 3 hours
- parameters measured: 13C content (continuous flow isotope ratio MS), % oxygen and % carbon dioxide (gas analyser), volume (dry gas meter), temperature (thermocouple within dry gas meter).
-collection times: 1 pre-ingestion sample and one after 3 hours (complete voiding of bladder)
- parameters measured: volume, pH, partial pressure CO2, urinary bicarbonate concentration (calculated) and acetate concentration.
-collection times: 1 pre-ingestion sample followed by samples every 30 minutes for 3 hours
- parameters measured: pH, base excess, O2 % saturation of haemoglobin, partial pressure of CO2, blood bicarbonate concentration, lactate, glycerol, FFA, acetate and haemoglobin concentrations

Results and discussion

Clinical signs:
Sodium acetate induced mild alkalosis, increased energy expenditure (p <0.05) but had no effect on fat or carbohydrate utilisation.
Results of examinations:
Ingestion of sodium acetate (2 mmol/kg bodyweight) resulted in a transient increase in plasma and urinary acetate concentrations. 80.1 ± 2.3% of the administered acetate was oxidized to CO2 and exhaled within 3h, 0.60 ± 0.09% was excreted unchanged in urine i.e. ~0.5 mg/kg bw acetate is removed per minute via the citric acid cycle.

Applicant's summary and conclusion

Following ingestion of 2 mmol/kg bw of acetate, 80.1% of dose was oxidised over the subsequent 3 hours.