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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Description of key information

Neodecanoyl chlorde is of moderate oral toxicity  and is very toxic via inhalation.

Key value for chemical safety assessment

Acute toxicity: via oral route

Endpoint conclusion
Dose descriptor:
LD50
Value:
1 760 mg/kg bw

Acute toxicity: via inhalation route

Endpoint conclusion
Dose descriptor:
LC50
Value:
400 mg/m³ air

Additional information

Sprague-Dawley rats (5/sex/dose) were exposed to NdCl in olive oil via gavage at doses of 1000, 1470, 2150, and 3160 mg/kg-bw (BASF, 1979). The number of deaths was as follows: 1/10 at 1000 mg/kg, 3/10at 1470 mg/kg6/10 at 2150 and10/10 at 3160 mg/kg Animals that died during the study had distension of the GI tract with diarrheic gut contents. No changes were noted at necropsy in animals that survived. The LD50value was 1760 mg/kg-bw in males and females.

 

In a guideline study (OECD TG 403), Wistar rats (5/sex/concentration) were exposed to NdCl as a vapor for four hours at analytical concentrations of 0, 0.12, 0.27, 0.41, and 0.62 mg/L and observed for 14 days (BASF, 1994). None of the animals exposed to 0.12 or 0.27 mg/L died. All 5 males and 2 females exposed to 0.41 mg/L died within 1 day. All animals exposed to 0.62 mg/L died during exposure. Accelerated and irregular respiration, grasping, snout wiping were noted. Gross pathology of animals that dies revealed hyperemia, oedema, and focal emphysema of the lungs. The 4-hr LC50value for males and females was 0.4 mg/L.

Justification for classification or non-classification

According to the results presented above neodecanoyl chloride is classified as very toxic by inhalation (acute inhal. Cat 1 and R26) and harmful after swallowing ((acute oral cat 4; R22). No classification suggested for acute dermal toxicity as criteria of regulations 67/548/EC and 1272/2008/EC are not met, no data is available, respectively.