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MilliporeSigma

158283

Lepidine

99%

Synonym(s):

4-Methylquinoline

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About This Item

Empirical Formula (Hill Notation):
C10H9N
CAS Number:
Molecular Weight:
143.19
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-734-2
Beilstein/REAXYS Number:
110926
MDL number:
Assay:
99%
Form:
liquid
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Quality Level

assay

99%

form

liquid

refractive index

n20/D 1.620 (lit.)

bp

261-263 °C (lit.)

mp

9-10 °C (lit.)

density

1.083 g/mL at 25 °C (lit.)

SMILES string

Cc1ccnc2ccccc12

InChI

1S/C10H9N/c1-8-6-7-11-10-5-3-2-4-9(8)10/h2-7H,1H3

InChI key

MUDSDYNRBDKLGK-UHFFFAOYSA-N

General description

Synthesis of lepidine from 4-anilinobutan-2-one in ethanol in the presence of HCl or FeCl3 has been reported. Nitration of lepidine has been reported.


pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter



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The Nitration of Lepidine and 2-Chlorolepidine.
Krahler SE and Burger A.
Journal of the American Chemical Society, 64(10), 2417-2419 (1942)
Mechanism of the Doebner-Miller lepidine synthesis.
Ogata Y, et al.
Journal of the Chemical Society B: Physical Organic, 805-810 (1969)
S L Pfaller et al.
Canadian journal of microbiology, 45(7), 623-626 (1999-09-25)
Strain Lep1, isolated from a bacterial consortium capable of aerobic degradation of 4-methylquinoline (4-MQ), was chosen for further characterization as it was the only member of the consortium able to grow on 4-MQ in pure culture. Lep1 was identified as



Global Trade Item Number

SKUGTIN
158283-100G04061838118196
158283-25G04061838743848