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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Acute Toxicity: oral

Currently viewing:

Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Study period:
1975
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Well document study, following standard protocols.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1975
Report date:
1975

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
EPA OTS 798.1175 (Acute Oral Toxicity)
GLP compliance:
not specified
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Phosphorous acid, diphenyl isodecyl ester
Molecular formula:
C22H31O3P
IUPAC Name:
Phosphorous acid, diphenyl isodecyl ester
Constituent 2
Chemical structure
Reference substance name:
Triphenyl phosphite
EC Number:
202-908-4
EC Name:
Triphenyl phosphite
Cas Number:
101-02-0
Molecular formula:
C18H15O3P
IUPAC Name:
triphenyl phosphite
Constituent 3
Chemical structure
Reference substance name:
Diisodecyl phenyl phosphite
EC Number:
247-098-3
EC Name:
Diisodecyl phenyl phosphite
Cas Number:
25550-98-5
Molecular formula:
C26H47O3P
IUPAC Name:
Reaction products of triphenyl phosphite and isodecanol (1:2)
Constituent 4
Reference substance name:
Grouped, low level constituents (1) - see description
Molecular formula:
C21H29O3P and C23H33O3P
IUPAC Name:
Grouped, low level constituents (1) - see description
Constituent 5
Reference substance name:
Grouped, low level constituents (2) - see description
Molecular formula:
N/A
IUPAC Name:
Grouped, low level constituents (2) - see description
Constituent 6
Chemical structure
Reference substance name:
Triisodecyl phosphite
EC Number:
246-998-3
EC Name:
Triisodecyl phosphite
Cas Number:
25448-25-3
Molecular formula:
C30H63O3P
IUPAC Name:
Phosphorus acid, triisodecyl ester
Constituent 7
Reference substance name:
Grouped, low level constituents (3) - see description
Molecular formula:
N/A
IUPAC Name:
Grouped, low level constituents (3) - see description
Test material form:
liquid

Test animals

Species:
rat
Strain:
CD-1
Sex:
male/female
Details on test animals or test system and environmental conditions:
Rats were obtained from Charles River UK.

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
corn oil
Details on oral exposure:
Rats were deprived of food for 18 hours prior to treatment and for a further 4 hours after treatment. Doses were administered by gastric intubation. All doses were adjusted to maintain a constant volume of 40 mL/kg.
Doses:
0.43, 0.75, 1.31, 2.30, 4.00, 6.90, 12.00 g/kg
No. of animals per sex per dose:
5 male and 5 female
Control animals:
no

Results and discussion

Effect levelsopen allclose all
Sex:
male
Dose descriptor:
LD50
Effect level:
3 840 mg/kg bw
Based on:
test mat.
95% CL:
2 910 - 5 060
Sex:
female
Dose descriptor:
LD50
Effect level:
6 730 mg/kg bw
Based on:
test mat.
95% CL:
4 710 - 9 630
Mortality:
No mortality was seen at doses up to and including 2300 mg/kg. Mortality was seen in 1 female rat and 3 male rats at 4000 mg/kg. All males rats in the 6900 and 12,000 mg/kg doses died. Two female rats in the 6900 mg/kg dose died and all died at 12,000 mg/kg.
Clinical signs:
other: Some clinical observations were observed at doses starting at 2300 mg/kg and up including hypoactivity, piloerection, diarrhea, tremors, and prostration.

Applicant's summary and conclusion

Interpretation of results:
sligthly toxic
Remarks:
Migrated information Criteria used for interpretation of results: expert judgment
Conclusions:
The acute effects in this study were all seen at doses of 2300 mg/kg and higher. Mortaility was observed in doses 4000 mg/kg and higher. Such high doses would generally not be used in modern guideline studies.
Executive summary:

The LD50s were determined to be 3840 mg/kg for males and 6730 for females. These LD50 are well above the level for classification.