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N,N'-methylenedimorpholine@ N,N'-methylenebismorpholine@ formaldehyde released from N,N'-methylenebismorpholine@ MBM

Identification RD1272 Classification Health risks Restrictions PDF

Identification

Name:
N,N'-methylenedimorpholine@ N,N'-methylenebismorpholine@ formaldehyde released from N,N'-methylenebismorpholine@ MBM
Synonyms:
  • N,N'-metilen-bismorfolina
  • formaldehído liberado de N,N'-metilen-bismorfolina
  • MBM
CAS:
5625-90-1
EC/EINECS:
227-062-3
Molecular Formula:
C9H18N2O2

Black list

Substances particularly hazardous to the environment or health

CLASSIFICATION AND LABELLING (Regulation 1272/2008)

Symbols

  • GHS05

    Corrosive to metals

  • GHS07

    Acute toxicity (oral, dermal, inhalation

  • GHS08

    Respiratory sensitisation

H Phrases

  • H350 : May cause cancer

    Carc. (Cat. 1B) : Carcinogenicity

  • H341 : Suspected of causing genetic defects

    Muta. (Cat. 2) : Germ cell mutagenicity

  • H332 : Harmful if inhaled

    Acute Tox. (Cat. 4) : Acute toxicity

  • H312 : Harmful in contact with skin

    Acute Tox. (Cat. 4) : Acute toxicity

  • H302 : Harmful if swallowed

    Acute Tox. (Cat. 4) : Acute toxicity

  • H373 : May cause damage to organs through prolonged or repeated exposure

    STOT RE (Cat. 2) : Specific target organ toxicity - repeated exposure

  • H314 : Causes severe skin burns and eye damage

    Skin Corr. (Cat. 1B) : Skin corrosion/irritation

  • H318 : Causes serious eye damage

    Eye Dam. (Cat. 1) : Serious eye damage/eye irritation

  • H317 : May cause an allergic skin reaction

    Skin Sens. (Cat. 1) : Respiratory/skin sensitization

Specific health risks

Carcinogens and mutagens (Regulation 1272/2008) ?

Substances classified as carcinogenic or mutagenic under Regulation 1272/2008

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Sensitisers ?

Substances with skin or respiratory sensitisation potential

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Restriction/prohibition regulations

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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