araldite-2011-sds

SAFETY DATA SHEET According to REACH Regulation (EC) No 1907/2006, as amended by UK REACH Regulations SI 2019/758 ARALDITE® 2011 HARDENER

Version 1 . 1

Revision Date: 27.09.2021

SDS Number: 400001015904

Date of last issue: 24.01.2018 Date of first issue: 24.01.2018

Print Date 14.09.2022

Result: negative Remarks: Information given is based on data obtained from similar substances.

Amines, polyethylenepoly-, triethylenetetramine fraction : Species: Mouse, male Dose: 42 mg/kg Frequency of Treatment: 3 daily No observed adverse effect level: >= 50 mg/kg bw/day Method: OECD Test Guideline 451 Result: negative Species: Mouse, male Application Route: Dermal Exposure time: 104 weeks Dose: 16.8 mg/kg Frequency of Treatment: 3 daily No observed adverse effect level: >= 20 mg/kg bw/day Method: OECD Test Guideline 451

Carcinogenicity - Assessment

: No data available

Reproductive toxicity

Components: N'-(3-aminopropyl)-N,N-dimethylpropane-1,3-diamine : Effects on fertility

: Test Type: OECD Test Guideline 422 Species: Rat, male and female Application Route: Oral Dose: 5, 15 and 50 mg/kg bw/d General Toxicity - Parent: No observed adverse effect level: 15 mg/kg body weight General Toxicity F1: No observed adverse effect level: 15 mg/kg body weight Method: OECD Test Guideline 422 Result: Animal testing did not show any effects on fertility. GLP: yes

Components: N'-(3-aminopropyl)-N,N-dimethylpropane-1,3-diamine : Effects on foetal development

: Species: Rat, male and female Application Route: Oral Dose: 5, 15 and 50 mg/kg bw/d General Toxicity Maternal: No observed adverse effect level: 15 mg/kg body weight Method: OECD Test Guideline 422 Result: Not classified GLP: yes

Amines, polyethylenepoly-, triethylenetetramine fraction : Test Type: Pre-natal Species: Rat Application Route: Oral

Dose: 75/325/750 mg/kg bw/day

SDS_GB-AM – 6N – 400001015904

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