Reaction mass of 1-Hydroxyoctane, 2-methanoate and 1,2-Dihydroxyoctane, dimethanoate and 2-Hydroxyoctane 1-methanoate and 1,2-Dihydroxyoctane

Acute Toxicity: oral

Administrative data

Endpoint:

acute toxicity: oral

Type of information:

experimental study

Adequacy of study:

key study

Study period:

22 Mar - 18 Apr 2016

Reliability:

1 (reliable without restriction)

Rationale for reliability incl. deficiencies:

guideline study

Data source

Reference

Reference Type:

study report

Title:

Unnamed

Year:

2016

Report date:

2016

Materials and methods

Test guideline

Qualifier:

according to guideline

Guideline:

OECD Guideline 423 (Acute Oral toxicity - Acute Toxic Class Method)

Version / remarks:

adopted 17 Dec 2001

Deviations:

no

GLP compliance:

yes

Test type:

acute toxic class method

Limit test:

no

Test material

Test material information

Constituent 1

Reference substance name:

Reaction mass of 1-Hydroxyoctane, 2-methanoate and 1,2-Dihydroxyoctane, dimethanoate and 2-Hydroxyoctane 1-methanoate and 1,2-Dihydroxyoctane

EC Number:

937-960-3

Molecular formula:

not applicabe (reaction mass)

IUPAC Name:

Reaction mass of 1-Hydroxyoctane, 2-methanoate and 1,2-Dihydroxyoctane, dimethanoate and 2-Hydroxyoctane 1-methanoate and 1,2-Dihydroxyoctane

Test animals

Species:

rat

Strain:

other: Crl:CD(SD), SPF

Sex:

female

Details on test animals or test system and environmental conditions:

TEST ANIMALS
- Age at study initiation: 8 - 9 weeks
- Weight at study initiation: 170.9 - 214.6 g
- Fasting period before study: overnight, approx. 16 h prior and 4 h after dosing
- Housing: 1 animale per cage in stainless wire mech cages (260W x 350D x 210H mm)
- Diet: Teklad Certified Irradiated Global 18% Protein Rodent Diet 2918C (Envigo RMS. Ltd., USA), ad libitum
- Water: public tap water filtered and irradiated by ultraviolet light, ad libitum
- Acclimation period: 4 days

ENVIRONMENTAL CONDITIONS
- Temperature (°C): 21.2 - 24.0
- Humidity (%): 43.5 - 58.5
- Air changes (per hr): 10 - 15
- Photoperiod (hrs dark / hrs light): 12/12

Administration / exposure

Route of administration:

oral: gavage

Vehicle:

corn oil

Details on oral exposure:

VEHICLE
- Lot/batch no.: MKBV2080V and MKBS6944V (SIGMA-ALDRICH, Co., USA)

MAXIMUM DOSE VOLUME APPLIED: 5 mL/kg bw

CLASS METHOD
- Rationale for the selection of the starting dose: The starting dose level for this study was selected at 300 mg/kg bw because there was no available toxicity information on the test substance.

Doses:

300 and 2000 mg/kg bw

No. of animals per sex per dose:

6

Control animals:

no

Details on study design:

- Duration of observation period following administration: 14 days
- Frequency of observations and weighing: Animals were observed 30 min and 1, 2, 4 and 6 h after dosing and thereafter once daily for 14 days. Individual body weights were recorded prior to dosing on Day 0 and on Days 1, 3, 7 and on the day of necropsy, Day 14.
- Necropsy of survivors performed: yes

Results and discussion

Effect levels

Key result

Sex:

female

Dose descriptor:

LD50

Effect level:

> 2 000 mg/kg bw

Based on:

test mat.

Remarks on result:

other: LD50 cut-off of 5000 mg/kg bw according to OECD 423

Mortality:

No mortality was observed at 300 and 2000 mg/kg bw, respectively.

Clinical signs:

other: Mucous stool was observed in two animals at 300 mg/kg bw on Day 1. The clinical sign disappeared on Day 2. Therefore, it was considered to be a test substance-related temporary change. No clinical abnormalities were observed in any animal at 2000 mg/kg bw

Gross pathology:

No grossly visible evidence of morphological abnormalities was observed in any animal at 300 and 2000 mg/kg bw, respectively.

Applicant's summary and conclusion

Interpretation of results:

other: CLP/EU GHS criteria not met, no classification required according to Regulation (EC) No 1272/2008

Conclusions:

In this acute oral toxicity study performed in rats a LD50 > 2000 mg/kg bw was found.

Executive summary:

There were no deaths of animals at 300 mg/kg. Mucous stool was observed in animals at 300 mg/kg on Day 1, and it disappeared on Day 2. No test substance-related effects were observed in body weight data or necropsy findings in any animal at 300 mg/kg.

There were no deaths of animals at 2,000 mg/kg. No test substance-related effects were observed in clinical signs, body weight data or necropsy findings in any animal at 2,000 mg/kg.

Based on the result of the acute oral toxicity study in Sprague-Dawley rats, the test substance was classified as Category 5 or Unclassified according to the GHS classification and the median lethal dose derived was: LD50 cut off≥ 5,000 mg/kg b.w.