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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Basic toxicokinetics

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Administrative data

Endpoint:
basic toxicokinetics in vivo
Type of information:
experimental study
Adequacy of study:
disregarded due to major methodological deficiencies
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: No details on study

Data source

Referenceopen allclose all

Reference Type:
publication
Title:
No information
Author:
OPDYKE DLJ
Year:
1977
Bibliographic source:
Food Cosmet Toxicol, 15(6), 633-638
Reference Type:
publication
Title:
No information
Author:
STRAND LP, SCHELINE RR
Year:
1975
Bibliographic source:
Xenobiotica, 5(1), 49-63

Materials and methods

Objective of study:
metabolism
Test guideline
Qualifier:
no guideline followed
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Vanillin
EC Number:
204-465-2
EC Name:
Vanillin
Cas Number:
121-33-5
Molecular formula:
C8H8O3
IUPAC Name:
1-butoxypropan-2-ol
Details on test material:
no data

Test animals

Species:
rat
Strain:
not specified
Sex:
not specified
Details on test animals or test system and environmental conditions:
no data

Administration / exposure

Route of administration:
oral: unspecified
Vehicle:
not specified
Details on exposure:
A single oral administration to rats of 100 mg/kg bw resulted in the urinary excretion of most of its metabolites within 24 hours, mainly as
glucuronide and/or sulphate conjugates, although the acids formed were also excreted free and as their glycine conjugates.
Duration and frequency of treatment / exposure:
no data
Doses / concentrations
Remarks:
Doses / Concentrations:
100 mg/kg bw
No. of animals per sex per dose / concentration:
no data
Control animals:
not specified

Results and discussion

Metabolite characterisation studies

Details on metabolites:
In 48 hours, 94% of the dose had been excreted, in the following proportions:
7% vanillin, 47% vanillic acid, 19% vanillyl alcohol, 10% vanilloylglycine, 8% catechol, 2% 4-methylcatechol, 0.6% 4-methylguaiacol, and 0.5% guaiacol.
No metabolites were found in the urine collected 48-96 hours after dosing.

Any other information on results incl. tables

The conversion of vanillin to vanillic acid was demonstrated in human and rat liver cells in culture (Discher & Brisse, 1966).

An early study found only traces amounts of vanillin in the urine of rabbits given 2g/day orally (about 1g/kg bw/day), the vanillin being conjugated with sulfuric acid. Most of the dose was oxidized to vanillic acid, and this too was excreted as ethereal sulfate conjugate (Preusse, 1880).

Applicant's summary and conclusion