RISCTOX

RISCTOX Database

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Identification

Name:
dibutyltin dilaurate@ dibutyl[bis(dodecanoyloxy)]stannane
Synonyms:
  • dibutil-[bis(dodecanoiloxi)]-estannano
CAS:
77-58-7
EC/EINECS:
201-039-8
Molecular Formula:
C32H64O4Sn
International Chemical Safety Card (ICSC):
1171

CLASSIFICATION AND LABELLING (Regulation 1272/2008)

Symbols

  • GHS08

    Respiratory sensitisation

H Phrases

  • H341 : Suspected of causing genetic defects

    Muta. (Cat. 2) : Germ cell mutagenicity

  • H360FD : May damage fertility. Suspected of damaging the unborn child.

    Repr. (Cat. 1B) : Reproductive toxicity

  • H372 : Causes damage to organs through prolonged or repeated exposure

    STOT RE (Cat. 1) : Specific target organ toxicity - repeated exposure

Specific health risks

According to IARC ?

Substances classified by the International Agency for Research on Cancer (IARC/WHO) according to their evidence of carcinogenicity in humans. Groups range from 1 (proven human carcinogen) to 4 (probably not carcinogenic to humans). The IARC classification is an international reference in occupational and environmental health.

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Prohibited for pregnant workers

Substances prohibited for pregnant workers

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Carcinogens and mutagens (Regulation 1272/2008) ?

Substances classified as carcinogenic or mutagenic under Regulation 1272/2008

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Reproductive toxicants ?

Substances classified as toxic for reproduction under Regulation 1272/2008

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Specific environmental risks

Hazardous water substances (Germany) ?

Substances classified with chronic aquatic toxicity under the CLP Regulation (H410–H413 phrases, Aquatic Chronic categories 1 to 4). They pose a long-term hazard to aquatic organisms, even at low concentrations and through prolonged exposure.

MMA Classification
3
List

Restriction/prohibition regulations

Substances subject to REACH authorization ?

Substances listed in Annex XIV of the REACH Regulation, subject to the prior authorisation scheme. To use them after the sunset date, companies must obtain authorisation from ECHA, demonstrating adequate risk control or the absence of viable alternatives.

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Substances under PACT evaluation ?

Substances under active regulatory monitoring through ECHA's PACT (Public Activities Coordination Tool). Allows tracking which regulatory authorities are examining a substance and what potential regulatory actions are being considered (restriction, SVHC identification, harmonised classification, etc.).

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