Tricyclic Antidepressants on Gemini 3u C18

LC Conditions

Column

Gemini 3 µm C18 110 Å, LC Column 150 x 4.6 mm, Ea

Brand

Gemini

Part No

00F-4439-E0

Phase Name

C18

Elution Type

Isocratic

Mobile Phase

A: 20mM Phosphate buffer, pH 7

B: Acetonitrile

C: Methanol

Gradient Profile

Step No.

Time(min)

Flow Rate

1.50 mL/min

Temperature

22°C

Detection

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

Detection Info

Sample Notes

SecurityGuard™ Guard Cartridge System extends column lifetime. - SecurityGuard Cartridges, Gemini C18 4 x 3.0mm, 10/Pk Part No.: AJ0-7597 - Holder Part No.: KJ0-4282

Order Items Used in This Application

00F-4439-E0

Gemini 3 µm C18 110 Å, LC Column 150 x 4.6 mm, Ea

View Product

1. Nortriptyline
2. Imipramine
3. Amitriptyline
4. Clomipramine

-OEChem-06211003152D<br><br> 41 43  0     0  0  0  0  0  0999 V2000<br>    3.1509   -2.0953    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.3830    3.0953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    5.3830    3.0953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.7595    2.3135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    6.0065    2.3135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.8830    0.9047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.9820    1.3386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    5.7840    1.3385    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.8830   -0.0953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.7690    2.6358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    6.9970    2.6358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.2295    0.6184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    6.5365    0.6184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.0170   -0.5953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.0000    1.9333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    7.7660    1.9332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.0169   -1.5953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.2318    0.9177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    7.5342    0.9177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.1509   -3.0953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.5210    3.6998    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.8244    3.3643    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    5.9416    3.3643    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    5.2450    3.6998    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    5.4199   -0.4053    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.6380    3.2418    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    7.1280    3.2418    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.3744    0.0156    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    6.3916    0.0155    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.8049   -0.0127    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.4064   -0.7030    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.2290   -2.1779    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.6275   -1.4877    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    1.4083    2.1183    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    8.3578    2.1182    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    1.7789    0.4943    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    7.9871    0.4942    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.6140   -1.7853    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.5309   -3.0953    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.1509   -3.7153    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.7709   -3.0953    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>  1 17  1  0  0  0  0<br>  1 20  1  0  0  0  0<br>  1 38  1  0  0  0  0<br>  2  3  1  0  0  0  0<br>  2  4  1  0  0  0  0<br>  2 21  1  0  0  0  0<br>  2 22  1  0  0  0  0<br>  3  5  1  0  0  0  0<br>  3 23  1  0  0  0  0<br>  3 24  1  0  0  0  0<br>  4  7  1  0  0  0  0<br>  4 10  2  0  0  0  0<br>  5  8  1  0  0  0  0<br>  5 11  2  0  0  0  0<br>  6  7  1  0  0  0  0<br>  6  8  1  0  0  0  0<br>  6  9  2  0  0  0  0<br>  7 12  2  0  0  0  0<br>  8 13  2  0  0  0  0<br>  9 14  1  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 16  1  0  0  0  0<br> 11 27  1  0  0  0  0<br> 12 18  1  0  0  0  0<br> 12 28  1  0  0  0  0<br> 13 19  1  0  0  0  0<br> 13 29  1  0  0  0  0<br> 14 17  1  0  0  0  0<br> 14 30  1  0  0  0  0<br> 14 31  1  0  0  0  0<br> 15 18  2  0  0  0  0<br> 15 34  1  0  0  0  0<br> 16 19  2  0  0  0  0<br> 16 35  1  0  0  0  0<br> 17 32  1  0  0  0  0<br> 17 33  1  0  0  0  0<br> 18 36  1  0  0  0  0<br> 19 37  1  0  0  0  0<br> 20 39  1  0  0  0  0<br> 20 40  1  0  0  0  0<br> 20 41  1  0  0  0  0<br>M  END

Compound Name

Nortriptyline

CID

4543

Molecular Formula

C19H21N

Molecular Weight

263

No. Hydrogen Bond Acceptors

No. Hydrogen Bond Donors

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