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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: other routes

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Administrative data

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

Data source

Referenceopen allclose all

Reference Type:
study report
Title:
Unnamed
Year:
1976
Report date:
1976
Reference Type:
other company data
Title:
Unnamed
Year:
2002
Report date:
2002

Materials and methods

Principles of method if other than guideline:
BASF Test: Several groups of 5 NMRI (Ivanova) mice per sex and dose were treated simultaneously i.p. with aqueous solutions of the test substance. Group-wise documentation of clinical signs was performed over the 14-day study period. Body weight was determined before the start of the study only, as it was needed for determination of dose. The clinical signs and findings were reported in summary form.
On the basis of the observed lethality, the LD50 value was estimated or determined using a graphical evaluation of the dose response curve on probability paper.
GLP compliance:
no
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
4-hydroxybutyl acrylate
EC Number:
219-606-3
EC Name:
4-hydroxybutyl acrylate
Cas Number:
2478-10-6
Molecular formula:
C7H12O3
IUPAC Name:
4-hydroxybutyl acrylate
Specific details on test material used for the study:
Test substance: Butanediolmonoacrylate
Chemical name: 2-Propenoic acid, 4-hydroxy ester

Test animals

Species:
mouse
Strain:
NMRI
Sex:
male/female
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Source: Ivanova
- Mean body weights at study initiation: males 26.7 g, females 24.0 g

Administration / exposure

Route of administration:
intraperitoneal
Vehicle:
water
Details on exposure:
MAXIMUM DOSE VOLUME APPLIED: 10 mL/kg bw
Doses:
1470, 1000, 681, 464, 316, and 215 µL/kg bw (corresponding to approx. 1529, 1040, 708, 483, 329, and 224 mg/kg bw)
Recalculation based on density = 1.04 g/cm3 at 25 °C (BASF AG, MSDS, 2007)
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:
Cageside observations were performed several times on the day of administration and daily on workdays during the observation period. Body weights were determined at test start only.
- Necropsy of survivors performed: yes
- Other examinations performed: clinical signs
Statistics:
no

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
ca. 483 - 708 mg/kg bw
Based on:
test mat.
Mortality:
At the two highest doses all treated animals died within the first hour after substance administration. At 708 mg/kg bw 7/10 animals died within 24 hrs, after 48 hrs 10/10 animals had expired. At the three lower doses, no mortality occurred.
Clinical signs:
Signs of toxicity comprised dyspnoea, apathy, lateral-abdominal position, staggering, twitching, saltatory convulsions, tremor, fibrillary convulsions, clonic convulsions, and poor general state.
Body weight:
Body weight gain during the course of the study was reported to be normal.
Gross pathology:
Deceased animals: liver degeneration.
Sacrificed animals: no adverse abnormalities observed at gross-pathological examination.

Any other information on results incl. tables

Original value: LD50 > 460 < 680 µL/kg bw; therefore LD50 > approx. 478 < approx. 707 mg/kg bw (density = 1.04 g/mL).

Mortality:

Dose [mg/kg bw]

Conc. [%]

No. of animals/sex

Dead animals / treated animals after

 

 

 

1 h

24 h

48 h

7 d

14 d

1529

14.7

5 m

5/5

5/5

5/5

5/5

5/5

5 f

5/5

5/5

5/5

5/5

5/5

1040

10

5 m

5/5

5/5

5/5

5/5

5/5

5 f

5/5

5/5

5/5

5/5

5/5

708

6.81

5 m

0/5

4/5

5/5

5/5

5/5

5 f

0/5

3/5

5/5

5/5

5/5

483

4.64

5 m

0/5

0/5

0/5

0/5

0/5

5 f

0/5

0/5

0/5

0/5

0/5

329

3.16

5 m

0/5

0/5

0/5

0/5

0/5

5 f

0/5

0/5

0/5

0/5

0/5

224

2.15

5 m

0/5

0/5

0/5

0/5

0/5

5 f

0/5

0/5

0/5

0/5

0/5

f: female

m: male

Applicant's summary and conclusion