| Identification | More | [Name]
Dodecyl isocyanate | [CAS]
4202-38-4 | [Synonyms]
1-DODECYL ISOCYANATE
DODECYL ISOCYANATE
LAURYL ISOCYANATE
N-DODECYL ISOCYANATE
1-isocyanato-dodecan
Dodecyl(lauryl) isocyanate
1-Dodecylisocyanate,98%
Isocyanic Acid Dodecyl Ester
1-Isocyanatododecane | [EINECS(EC#)]
224-111-0 | [Molecular Formula]
C13H25NO | [MDL Number]
MFCD00041744 | [Molecular Weight]
211.34 | [MOL File]
4202-38-4.mol |
| Chemical Properties | Back Directory | [Appearance]
clear colorless to light yellowish liquid | [Boiling point ]
157-161 °C/21 mmHg (lit.) | [density ]
0.877 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.441(lit.)
| [Fp ]
>230 °F
| [storage temp. ]
0-10°C | [form ]
clear liquid to slightly cloudy liquid | [color ]
Colorless to Almost colorless | [Water Solubility ]
negligible soluble | [Sensitive ]
Moisture Sensitive | [BRN ]
1774823 | [CAS DataBase Reference]
4202-38-4(CAS DataBase Reference) | [EPA Substance Registry System]
4202-38-4(EPA Substance) |
| Safety Data | Back Directory | [Hazard Codes ]
Xn | [Risk Statements ]
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
R36/37/38:Irritating to eyes, respiratory system and skin .
R41:Risk of serious damage to eyes.
R42:May cause sensitization by inhalation. | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
S37/39:Wear suitable gloves and eye/face protection .
S23:Do not breathe gas/fumes/vapor/spray (appropriate wording to be specified by the manufacturer) . | [RIDADR ]
UN 2206 6.1/PG 3
| [WGK Germany ]
3
| [TSCA ]
Yes | [HS Code ]
2929.10.8090 | [HazardClass ]
6.1 | [PackingGroup ]
III |
| Hazard Information | Back Directory | [Chemical Properties]
clear colorless to light yellowish liquid | [Uses]
1-Dodecyl isocyanate, is incorporated in AZT analogue preparation through it use ine the synthesis of carbodiimides from phosphinimines. |
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