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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

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Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
supporting study
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: Older guideline-comparable study reported in summary form

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1977
Report date:
1977

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 401 (Acute Oral Toxicity)
Principles of method if other than guideline:
The test method is comparable to the withdrawn OECD TG 401
GLP compliance:
no
Remarks:
: the study pre-dates GLP
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Phosphoryl trichloride
EC Number:
233-046-7
EC Name:
Phosphoryl trichloride
Cas Number:
10025-87-3
Molecular formula:
Cl3OP
IUPAC Name:
phosphoroyl trichloride
Test material form:
liquid: volatile
Details on test material:
The test material 'MCTR-191-77' is stated to be a colourless, transparent, viscous and volatile liquid.

Test animals

Species:
rat
Strain:
Sprague-Dawley
Sex:
male/female
Details on test animals or test system and environmental conditions:
A total of 50 male and female rats weighing between 200 and 300 grams, were fasted for approximately 24 hours prior to the administration of the test material.

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
corn oil
Details on oral exposure:
The test material sample 'MCTR-191-77' (=phosphoryl trichloride) was administered on a mg/kg basis as a 10% solution in corn oil.
Doses:
The dose levels of the test substance included in the study were 50, 100, 200, 300 and 400 mg/kg bw.
No. of animals per sex per dose:
Ten animals (male and female; not speciifed further)
Control animals:
no
Details on study design:
The animals were observed at 1, 3, 6, 24, 72 and daily thereafter for a total of 14 days if survival allowed and then killed, autopsied and observed for gross pathological organ changes.
Statistics:
None required

Results and discussion

Preliminary study:
None
Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
110 mg/kg bw
Based on:
test mat.
95% CL:
> 91 - < 129
Remarks on result:
other: Calculated according to the method of Miller & Tainter, 1944.
Mortality:
Two deaths were recorded after rats were administered with the 50 mg/kg dose, 4 deaths were recorded following the 100 mg/kg dose, 9 deaths were recorded following the 200 mg/kg dose, 9 deaths were recorded following the 300 mg/kg dose and 10 deaths were recorded following the 400 mg/kg dose
Clinical signs:
other: Decreased locomotor activity, piloerection, ptosis, suspected blood around the eyes, loss of righting reflex and death. Chronic pulmonary disease was revealed at 50, 100 and 200 mg/kg body weight. Normal body activity returned within 7 days in all surviv
Gross pathology:
Autopsies revealed lung fused to the rib cage in rats adminstered with the 50 mg/kg dose level. At 100 mg/kg there appeared to be lung fused to the rib cage and filled with a white mass, with irregular thickening on the cardiac mucosa
Other findings:
None

Any other information on results incl. tables

Distribution of Mortality

Dose (mg/kg bw)

Deaths

Hour

Observation Day

1

3

6

1

2

3

4

5

6

7

8

9

10

11

12

13

14

50

2/10

0

0

0

1

0

0

0

1

0

0

0

0

0

0

0

0

0

100

4/10

0

0

0

1

2

0

0

0

1

0

0

0

0

0

0

0

0

200

9/10

1

7

0

1

0

0

0

0

0

0

0

0

0

0

0

0

0

300

9/10

4

5

0

0

0

0

0

0

0

0

0

0

0

0

0

0

0

400

10/10

4

5

0

1

-

-

-

-

-

-

-

-

-

-

-

-

-

 

Applicant's summary and conclusion

Interpretation of results:
Category 3 based on GHS criteria
Conclusions:
The acute oral LD50 of phosphoryl trichloride in the rat was found to be 110 mg/kg bw under the conditions of this study. Based on these results, 'MCTR-191-77' is classified with Acute Tox. 3 (H301, Toxic if swallowed) according to GHS criteria.
Executive summary:

Groups of ten male and female Sprague-Dawley rats were gavaged with single doses of phosphoryl trichloride (10% in corn oil) at dose levels of 50, 100, 200, 300 or 400 mg/kg bw and observed for 14 days. Gross necropsy was performed on all animals.

 

Thirty-four deaths were recorded following administration of the test substance, with the majority of deaths occurring in the higher dose level groups. The following signs of toxicity were observed: decreased locomotor activity, piloerection, ptosis, suspected blood around the eyes, loss of righting reflex and death.  Chronic pulmonary disease was revealed at dose levels of 50, 100 and 200 mg/kg bw.  Normal activity returned within seven days in all surviving animals. Autopsies revealed lung fused to the rib cage in rats administered 50 mg/kg bw. At 100 mg/kg bw there appeared to be lung fused to the rib cage and filled with a white mass, with irregular thickening of the cardiac mucosa

The acute oral LD50 in the rat was calculated to be 110 mg/kg bw under the conditions of this study.