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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Administrative data

Endpoint:
acute toxicity: inhalation
Type of information:
experimental study
Adequacy of study:
supporting study
Study period:
December 1977
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
study well documented, meets generally accepted scientific principles, acceptable for assessment

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1978
Report date:
1978

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
- Principle of test: 1-hr inhalation exposure
- Short description of test conditions: rats are exposed for 1 hour to 2 mg/L air and then observed during 14 days
- Parameters analysed / observed: clinical signs, mortality, body weight, autopsie
GLP compliance:
no
Test type:
fixed concentration procedure

Test material

Constituent 1
Chemical structure
Reference substance name:
2-thienylacetyl chloride
EC Number:
254-290-0
EC Name:
2-thienylacetyl chloride
Cas Number:
39098-97-0
Molecular formula:
C6H5ClOS
IUPAC Name:
2-thienylacetyl chloride
Test material form:
liquid
Details on test material:
- Density: 1.29

Test animals

Species:
rat
Strain:
Sprague-Dawley
Sex:
male/female
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Source: no data
- Females (if applicable) nulliparous and non-pregnant: no data
- Age at study initiation: no data
- Weight at study initiation: 202.8g for males and 190.2g for females on D0 (mean value)
- Fasting period before study: no data
- Diet (e.g. ad libitum): no data
- Water (e.g. ad libitum): no data
- Acclimation period: no data

ENVIRONMENTAL CONDITIONS
- Temperature (°C): no data
- Humidity (%): no data
- Air changes: around 10/hours
- Photoperiod (hrs dark / hrs light): no data

IN-LIFE DATES: no data

Administration / exposure

Route of administration:
inhalation: vapour
Type of inhalation exposure:
whole body
Vehicle:
air
Details on inhalation exposure:
GENERATION OF TEST ATMOSPHERE / CHAMBER DESCRIPTION
A parallelepipedic glass vessel, 100L in volume, is continuously crossed by the atmosphere overloaded with the product. These vapors are obtained by creating a vaporization of the product inside a glass column: this column is fed, on the one hand, with compressed air at a known and adjustable flow rate and, on the other hand, with the liquid substance also arriving at a determined rate by means of a syringe infuser (Perfusor Braun).
This 100L vessel is crossed by the overloaded atmosphere with a flow rate of approximately 1 m3 per hour. A ventilator located inside the vessel homogenises continuously the atmosphere.
Analytical verification of test atmosphere concentrations:
no
Duration of exposure:
1 h
Concentrations:
2.05 mg/L
No. of animals per sex per dose:
5
Control animals:
no
Details on study design:
- Duration of observation period following administration: 14 days
- Frequency of observations and weighing: weighing D0, 2, 4, 7 and 14
- Necropsy of survivors performed: yes
- Other examinations performed: clinical signs

Results and discussion

Effect levelsopen allclose all
Sex:
male/female
Dose descriptor:
LC50
Effect level:
> 2.05 mg/L air
Based on:
test mat.
Exp. duration:
1 h
Sex:
male/female
Dose descriptor:
LC0
Effect level:
>= 2.05 mg/L air
Based on:
test mat.
Exp. duration:
1 h
Mortality:
no mortality
Clinical signs:
other: during the exposure: attempted escape, hyperactivity, closing of the palpebral fissure, sneezing, trembling, loose breathing movements. after the exposure: tachycardia (D0-1), hyperactivity (D0-4), then normal behavior.
Body weight:
no effect
Gross pathology:
whitish mottling and numerous red spots in the lungs in several animals.
gastric mucous irritation in one female.

Applicant's summary and conclusion

Interpretation of results:
study cannot be used for classification
Conclusions:
In this study in rats the 1-hr LC0 is 2.05 mg/L (no mortality is observed).
Executive summary:

In an acute inhalation toxicity study, groups of Sprague-Dawley rats (5/sex) were exposed by inhalation route to 2-thienylacetyl chloride for 1 hour (whole body) at concentration of 2.05 mg/L.  Animals then were observed for 14 days.

LC0 Combined = 2.05 mg/L (no mortality occurred)