| Identification | More | [Name]
N-Isopropylethylenediamine | [CAS]
19522-67-9 | [Synonyms]
2-(ISOPROPYLAMINO)ETHYLAMINE
N-ISOPROPYLETHYLENEDIAMINE
RARECHEM AL BW 2006
1,2-Ethanediamine, N-(1-methylethyl)-
Ethylenediamine, N-isopropyl-
Isopropylaminoethylamine
n-(1-methylethyl)-2-ethanediamine
N-(2-aminoethyl)-N-isopropylamine
N-Isopropyl-1,2-ethanediamine
N-Isopropylethane-1,2-diamine | [EINECS(EC#)]
243-125-8 | [Molecular Formula]
C5H14N2 | [MDL Number]
MFCD00008164 | [Molecular Weight]
102.18 | [MOL File]
19522-67-9.mol |
| Safety Data | Back Directory | [Hazard Codes ]
F,C | [Risk Statements ]
R11:Highly Flammable.
R34:Causes burns. | [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) .
S16:Keep away from sources of ignition-No smoking . | [RIDADR ]
UN 2733 3/PG 2
| [WGK Germany ]
3
| [F ]
10-23 | [HazardClass ]
3 | [PackingGroup ]
II | [HS Code ]
29212900 |
| Hazard Information | Back Directory | [Chemical Properties]
Colorless to light yellow liqui | [Uses]
3-Hydroxy-1-(4-methoxyphenyl)-4-phenyl-2-azetidinone is used as a reagent in the preparation of enantiopure α-hydroxy-β-lactams via stereoselective glycosylation. | [Definition]
ChEBI: A primary aliphatic amine that is ethane-1,2-diamine substituted by an isopropyl group at the N atom. |
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