Doxylamine impurity profile on Kinetex 2.6 µm EVO C18

Doxylamine impurity profile on Kinetex 2.6 µm EVO C18
LC Conditions
Column

Kinetex 2.6 µm EVO C18 100 Å, LC Column 50 x 2.1 mm, Ea

Brand

Kinetex

Part No

00B-4725-AN

Phase Name

EVO C18

Elution Type

Gradient

Mobile Phase

A: 20 mM ammonium bicarbonate pH 10.0

B: Acetonitrile

Gradient Profile

Step No.

Time(min)

%A

%B

1

0

95

5

2

5

5

95

Flow Rate

0.70 mL/min

Temperature

22°C

Detection

UV-Vis Abs.-Variable Wave.(UV) @ (22°C)

Detection Info
Sample Notes

Forced degradation protocol: Reconstitute 1 mg of cefaclor neat standard with 1.0 mL of 1 M HCl. Heat the solution at 60 ºC for 6 hours then neutralize with 1.0 mL of 1 M NaOH. Refrigerate until ready to inject.

Order Items Used in This Application

Kinetex 2.6 µm EVO C18 100 Å, LC Column 50 x 2.1 mm, Ea
00B-4725-AN

Kinetex 2.6 µm EVO C18 100 Å, LC Column 50 x 2.1 mm, Ea

View Product

  • 1. Doxylamine
-OEChem-06211003152D<br><br> 42 43  0     1  0  0  0  0  0999 V2000<br>    4.0000    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0<br>    6.0000   -1.7320    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.8660   -1.5000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.0000    0.0000    0.0000 C   0  0  3  0  0  0  0  0  0  0  0  0<br>    3.0000    1.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.0000   -1.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.5000   -0.8660    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    5.5000   -0.8660    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.1340    1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.8660    1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.1340   -1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.1340    2.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.8660    2.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.1340   -2.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.0000    3.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    7.0000   -1.7320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    5.5000   -2.5981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.8660   -2.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.0000   -3.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.0000    0.6200    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    1.3800    0.0000    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.0000   -0.6200    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.9174   -1.0781    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.6077   -1.4766    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    6.0826   -0.6540    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    5.3923   -0.2554    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    1.5970    1.1900    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.4030    1.1900    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    1.5970   -1.1900    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    1.5970    2.8100    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.4030    2.8100    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    1.5970   -2.8100    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.0000    3.6200    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    7.0000   -2.3521    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    7.6200   -1.7320    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    7.0000   -1.1120    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.9631   -2.2881    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    5.1900   -3.1350    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    6.0369   -2.9081    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.4030   -2.8100    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.0000   -3.6200    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>  1  4  1  0  0  0  0<br>  1  8  1  0  0  0  0<br>  2  9  1  0  0  0  0<br>  2 17  1  0  0  0  0<br>  2 18  1  0  0  0  0<br>  3  6  1  0  0  0  0<br>  3 19  2  0  0  0  0<br>  4  5  1  0  0  0  0<br>  4  6  1  0  0  0  0<br>  4  7  1  0  0  0  0<br>  5 10  2  0  0  0  0<br>  5 11  1  0  0  0  0<br>  6 12  2  0  0  0  0<br>  7 21  1  0  0  0  0<br>  7 22  1  0  0  0  0<br>  7 23  1  0  0  0  0<br>  8  9  1  0  0  0  0<br>  8 24  1  0  0  0  0<br>  8 25  1  0  0  0  0<br>  9 26  1  0  0  0  0<br>  9 27  1  0  0  0  0<br> 10 13  1  0  0  0  0<br> 10 28  1  0  0  0  0<br> 11 14  2  0  0  0  0<br> 11 29  1  0  0  0  0<br> 12 15  1  0  0  0  0<br> 12 30  1  0  0  0  0<br> 13 16  2  0  0  0  0<br> 13 31  1  0  0  0  0<br> 14 16  1  0  0  0  0<br> 14 32  1  0  0  0  0<br> 15 20  2  0  0  0  0<br> 15 33  1  0  0  0  0<br> 16 34  1  0  0  0  0<br> 17 35  1  0  0  0  0<br> 17 36  1  0  0  0  0<br> 17 37  1  0  0  0  0<br> 18 38  1  0  0  0  0<br> 18 39  1  0  0  0  0<br> 18 40  1  0  0  0  0<br> 19 20  1  0  0  0  0<br> 19 41  1  0  0  0  0<br> 20 42  1  0  0  0  0<br>M  END
Compound Name

Doxylamine

CID

3162

Molecular Formula

C17H22N2O

Molecular Weight

270

No. Hydrogen Bond Acceptors

3

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