Pheniramine and Halogenated Derivatives on Kinetex 2.6u EVO C18 100x4.6mm

Pheniramine and Halogenated Derivatives on Kinetex 2.6u EVO C18 100x4.6mm
LC Conditions
Column

Kinetex 2.6 µm EVO C18 100 Å, LC Column 100 x 4.6 mm, EA

Brand

Kinetex

Part No

00D-4725-E0

Phase Name

EVO C18

Elution Type

Gradient

Mobile Phase

A: 10mM Ammonium Bicarbonate, pH=10.2

B: Acetonitrile

Gradient Profile

Step No.

Time(min)

%A

%B

1

0

50

50

2

4

40

60

Flow Rate

1.25 mL/min

Temperature

25°C

Detection

UV-Vis Abs.-Diode Array (PDA) @ (25°C)

Detection Info

Order Items Used in This Application

Kinetex 2.6 µm EVO C18 100 Å, LC Column 100 x 4.6 mm, EA
00D-4725-E0

Kinetex 2.6 µm EVO C18 100 Å, LC Column 100 x 4.6 mm, EA

View Product

  • 1. Pheniramine
  • 2. Chlorpheniramine
  • 3. Brompheniramine
-OEChem-06211003152D<br><br> 38 39  0     1  0  0  0  0  0999 V2000<br>    2.8660    2.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0<br>    5.4641   -1.5000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.5981    0.0000    0.0000 C   0  0  3  0  0  0  0  0  0  0  0  0<br>    3.7320    0.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.7320    1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    5.4641    0.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.5981   -1.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    6.3301    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    5.4641    1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.7320   -1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.8660    3.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.0000    1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    7.1962    0.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    6.3301    2.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.7320   -2.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    7.1962    1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    5.4641   -2.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.5981   -3.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.5981    0.6200    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.1215    0.6077    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.5200   -0.0826    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.3426    1.3923    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.9441    2.0826    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    6.3301   -0.6200    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.9272    1.8100    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.1951   -1.1900    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.4860    3.0000    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.8660    3.6200    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.2460    3.0000    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    1.6900    2.0369    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    1.4631    1.1900    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.3100    0.9631    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    7.7331    0.1900    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    6.3301    2.6200    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.1951   -2.8100    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    7.7331    1.8100    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    6.0010   -2.8100    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.5981   -3.6200    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>  1  5  1  0  0  0  0<br>  1 11  1  0  0  0  0<br>  1 12  1  0  0  0  0<br>  2  7  1  0  0  0  0<br>  2 17  2  0  0  0  0<br>  3  4  1  0  0  0  0<br>  3  6  1  0  0  0  0<br>  3  7  1  0  0  0  0<br>  3 19  1  0  0  0  0<br>  4  5  1  0  0  0  0<br>  4 20  1  0  0  0  0<br>  4 21  1  0  0  0  0<br>  5 22  1  0  0  0  0<br>  5 23  1  0  0  0  0<br>  6  8  2  0  0  0  0<br>  6  9  1  0  0  0  0<br>  7 10  2  0  0  0  0<br>  8 13  1  0  0  0  0<br>  8 24  1  0  0  0  0<br>  9 14  2  0  0  0  0<br>  9 25  1  0  0  0  0<br> 10 15  1  0  0  0  0<br> 10 26  1  0  0  0  0<br> 11 27  1  0  0  0  0<br> 11 28  1  0  0  0  0<br> 11 29  1  0  0  0  0<br> 12 30  1  0  0  0  0<br> 12 31  1  0  0  0  0<br> 12 32  1  0  0  0  0<br> 13 16  2  0  0  0  0<br> 13 33  1  0  0  0  0<br> 14 16  1  0  0  0  0<br> 14 34  1  0  0  0  0<br> 15 18  2  0  0  0  0<br> 15 35  1  0  0  0  0<br> 16 36  1  0  0  0  0<br> 17 18  1  0  0  0  0<br> 17 37  1  0  0  0  0<br> 18 38  1  0  0  0  0<br>M  END
Compound Name

Pheniramine

CID

4761

Molecular Formula

C16H20N2

Molecular Weight

240

No. Hydrogen Bond Acceptors

2

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