Pregabalin Impurity 50

Pregabalin Impurity 50
Catalog No. KMP004075
CAS No. 350801-73-9
Formula C8H12NO2 : K
FW 154.2 : 39.1
Unit Price Stock
100 mg Enquire Enquire
Chemical Name Potassium (S)-3-cyano-5-methylhexanoate
Purity >95%
Storage Store at 2-8 deg. C for long term storage
Shipping Product is stable to be Shipped at Room Temperature
Download MSDS

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Pregabalin Impurity 40

Pregabalin Impurity 40

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Pregabalin Impurity 43

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Pregabalin Lactose Conjugate Impurity 2

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Rac-Pregabalin Imide Dimer Amide

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Formula : C16H32N2O3

FW : 300.4

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Pregabalin Impurity 41

CAS No. : NA

CAT No. : KMP004066

Formula : C9H17NO2

FW : 171.2

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Pregabalin Impurity 7

Pregabalin Impurity 7

CAS No. : 1374336-43-2

CAT No. : KMP004091

Formula : C10H17NO2

FW : 183.3

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Pregabalin D4

Pregabalin D4

CAS No. : 1276197-54-6

CAT No. : KMP004027

Formula : C8H13D4NO2

FW : 163.3

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Pregabalin D6

Pregabalin D6

CAS No. : NA

CAT No. : KMP004028

Formula : C8H11D6NO2

FW : 165.3

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N-Nitroso Pregabalin

N-Nitroso Pregabalin

CAS No. : NA

CAT No. : KMP004021

Formula : C8H16N2O3

FW : 188.2

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Isobutylglutarmonoamide (R-isomer)

Isobutylglutarmonoamide (R-isomer)

CAS No. : 181289-33-8

CAT No. : KMP004019

Formula : C9H17NO3

FW : 187.2

View Details
Pregabalin EP Impurity A

Pregabalin EP Impurity A

CAS No. : 181289-23-6

CAT No. : KMP004035

Formula : C8H15NO

FW : 141.2

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Pregabalin EP Impurity B

Pregabalin EP Impurity B

CAS No. : 148553-51-9

CAT No. : KMP004036

Formula : C8H17NO2

FW : 159.2

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Pregabalin EP Impurity C

Pregabalin EP Impurity C

CAS No. : 90-64-2

CAT No. : KMP004037

Formula : C8H8O3

FW : 152.2

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Pregabalin EP Impurity D

Pregabalin EP Impurity D

CAS No. : 4118-51-8

CAT No. : KMP004038

Formula : C11H14O3

FW : 194.2

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Pregabalin USP Related Compound C

Pregabalin USP Related Compound C

CAS No. : 61312-87-6

CAT No. : KMP004106

Formula : C8H15NO

FW : 141.2

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About Us

K. M. Pharma Solution Pvt. Ltd., India (CIN: U72100GJ2023PTC141278), is a leading, innovation-driven company accredited by FDCA, GMP-GLP, ISO 9001:2015, and NABL (ISO/IEC 17025 & ISO 17034). Specializing in the design, synthesis, and characterization of pharmaceutical impurity standards and reference materials, we offer an extensive portfolio including nitrosamine impurities, pharmacopeial and non-pharmacopeial impurities, drug metabolites, glucuronides, process degradants, excipient-related impurities, unknown impurity isolation & structural elucidation, and stable isotope-labeled compounds.

As an integrated Contract Research, Development & Manufacturing Organization (CRDMO), we provide end-to-end scientific services — from early-stage discovery through to commercial supply — with a strong focus on quality, compliance, and customer satisfaction.

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