| Identification | More | [Name]
N-(2-Hydroxyethyl)-N-methylaniline | [CAS]
93-90-3 | [Synonyms]
2-(METHYLPHENYLAMINO)ETHANOL
2-(N-METHYLANILINO)ETHANOL
N-(2-HYDROXYETHYL)-N-METHYLANILINE
N-BETA-HYDROXYETHYL-N-METHYLANILINE
N-B-HYDROXYETHYL-N-METHYLANILINE
N-HYDROXYETHYL-N-METHYL ANILINE
N-METHYL-N-2-ETHANOLANILINE
N-METHYL-N-HYDROXYETHYL ANILINE
N-METHYL-N-PHENYLETHANOLAMINE
N-PHENYL-N-METHYLETHANOLAMINE
TIMTEC-BB SBB007818
2-(Methylanilino)ethanol
2-(methylphenylamino)-ethano
2-(N-Fenyl-N-methylamino)ethanol
2-(N-Methylaniline)ethanol
2-(n-methylanilino)-ethano
2-(N-Methyl-N-phenylamino)ethanol
Ethanol, 2-(methylphenylamino)-
Ethanol, 2-(N-methylanilino)-
Ethanol,2-(methylphenylamino)- | [EINECS(EC#)]
202-285-9 | [Molecular Formula]
C9H13NO | [MDL Number]
MFCD00020572 | [Molecular Weight]
151.21 | [MOL File]
93-90-3.mol |
| Chemical Properties | Back Directory | [Melting point ]
77 °C | [Boiling point ]
229 °C (lit.) | [density ]
1.06 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.573(lit.)
| [Fp ]
>230 °F
| [storage temp. ]
Keep in dark place,Inert atmosphere,Room temperature | [form ]
clear liquid | [pka]
14.79±0.10(Predicted) | [color ]
Light yellow to Brown | [Specific Gravity]
1.071.060 | [Detection Methods]
HPLC | [InChI]
InChI=1S/C9H13NO/c1-10(7-8-11)9-5-3-2-4-6-9/h2-6,11H,7-8H2,1H3 | [InChIKey]
VIIZJXNVVJKISZ-UHFFFAOYSA-N | [SMILES]
C(O)CN(C)C1=CC=CC=C1 | [CAS DataBase Reference]
93-90-3(CAS DataBase Reference) | [NIST Chemistry Reference]
N-(2-Hydroxyethyl)-N-methylaniline(93-90-3) | [EPA Substance Registry System]
93-90-3(EPA Substance) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [WGK Germany ]
2
| [RTECS ]
KL7175000
| [HS Code ]
29221990 |
| Hazard Information | Back Directory | [Chemical Properties]
Colorless to yellow liquid | [Uses]
Octaacetyl-β-maltose is used to prepare self-reproducing micelles in the preparation of triazole-containing disaccharides. It has also been used as a reactant in the synthesis of neoglycoconjugates through glycosyl aldehydes featuring bioorthogonal oxime bond formation. |
|
|