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You Searched For: 3-Carbamyl-1-methylpyridinium+chloride


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3-Carbamyl-1-methylpyridinium chloride ≥98.0% (by HPLC, titration analysis)

Supplier: TCI America
Description: CAS Number: 1005-24-9
MDL Number: MFCD00060042
Molecular Formula: C7H9ClN2O
Molecular Weight: 172.61
Purity/Analysis Method: >98.0% (HPLC,T)
Form: Crystal

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Image Unavailable-TCB4828-5G

Bethanechol chloride ≥98.0% (by titrimetric analysis)

Supplier: TCI America
Description: Bethanechol Chloride, Purity: >98.0%(T), Cas no. 590-63-6, Molecular formula: C7H17ClN2O2, Form: Crystal - Powder, Colour: White - Almost white, Synonyms: (2-Carbamoyloxypropyl)trimethylammonium Chloride, Carbamyl-B-methylcholine Chloride, Size: 25G

SDS

Image Unavailable-TCB3426-5G

1-Butyl-4-methylpyridinium chloride ≥99.0% (by HPLC, titration analysis)

Supplier: TCI America
Description: CAS Number: 112400-86-9
MDL Number: MFCD03095439
Molecular Formula: C10H16ClN
Molecular Weight: 185.70
Purity/Analysis Method: >99.0% (HPLC,T)
Form: Crystal
Melting point (°C): 160

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Image Unavailable-TCB3425-1G

1-Butyl-3-methylpyridinium chloride ≥98.0% (by HPLC, titration analysis)

Supplier: TCI America
Description: CAS Number: 125652-55-3
MDL Number: MFCD08458942
Molecular Formula: C10H16ClN
Molecular Weight: 185.70
Purity/Analysis Method: >98.0% (HPLC,T)
Form: Crystal

SDS

Image Unavailable-TCH0967-005G

1-Hexadecyl-4-methylpyridinium chloride hydrate

Catalog Number: (TCH0967-005G)
Supplier: TCI America
Description: CAS Number: 13106-53-1
MDL Number: MFCD02093475
Molecular Formula: C22H40ClN
Molecular Weight: 354.02
Form: Crystal
Color: White

SDS


Image Unavailable-TCT1429-005G

Trigonelline hydrochloride ≥98.0% (by HPLC, titration analysis)

Catalog Number: (TCT1429-005G)
Supplier: TCI America
Description: CAS Number: 6138-41-6
MDL Number: MFCD00077250
Molecular Formula: C7H8ClNO2
Molecular Weight: 173.60
Purity/Analysis Method: >98.0% (HPLC,T)
Form: Crystal
Color: White

SDS Certificates


Image Unavailable-TCM0819-025G

Pyridine-2-aldoxime methochloride ≥98.0% (by HPLC, titration analysis)

Catalog Number: (TCM0819-025G)
Supplier: TCI America
Description: CAS Number: 51-15-0
MDL Number: MFCD00011981
Molecular Formula: C7H9ClN2O
Molecular Weight: 172.61
Purity/Analysis Method: >98.0% (HPLC,T)
Form: Crystal

SDS


Image Unavailable-89160-446

1-O-Hexadecyl-2-N-methylcarbamyl-sn-glycero-3-phosphocholine ≥98% (by TLC)

Catalog Number: (89160-446)
Supplier: Enzo Life Sciences
Description: PAF receptor activator.
Product Image-77527-598

Human anti-CarP (anti-carbamylated protein) ELISA Kit

Catalog Number: (77527-598)
Supplier: AFG BIOSCIENCE LLC
Description: Human anti-CarP (anti-carbamylated protein) ELISA Kit

New Product


Product Image-76732-798

Human Carbamylated Albumin ELISA Kit

Catalog Number: (76732-798)
Supplier: ANTIBODIES.COM LLC
Description: Human Carbamylated Albumin ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the <i>in vitro</i> quantitative determination of human Carbamylated Albumin in serum, plasma, tissue homogenates, and other biological fluids.
Product Image-76740-998

Human Anti-Carbamylated Protein Antibody ELISA Kit

Catalog Number: (76740-998)
Supplier: ANTIBODIES.COM LLC
Description: Human Anti-Carbamylated Protein Antibody ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the <i>in vitro</i> quantitative determination of human Anti-Carbamylated Protein Antibody in serum, plasma, tissue homogenates, and other biological fluids.
Image Unavailable-76220-042

1-Ethyl-2-methylpyridinium bromide ≥98.0% (by HPLC, titration analysis)

Supplier: TCI America
Description: 1-Ethyl-2-methylpyridinium Bromide, Purity: >98.0%(HPLC)(T), CAS number: 32353-50-7, Molecular Formula: C8H12BrN, Molecular Weight: 202.10, Form: Crystal - Powder, White - Pale reddish yellow, Size: 5G

Product Image-76700-518

Human Aniti-Carbamylated Protein Antibody(Carp-Ab) ELI SA Kit

Catalog Number: (76700-518)
Supplier: AFG BIOSCIENCE LLC
Description: Human Aniti-Carbamylated Protein Antibody(Carp-Ab) ELI SA Kit
Image Unavailable-10481-148

Anti-DPYS Rabbit Polyclonal Antibody (Cy3®)

Catalog Number: (10481-148)
Supplier: Bioss
Description: Catalyzes the second step of the reductive pyrimidine degradation, the reversible hydrolytic ring opening of dihydropyrimidines. Can catalyzes the ring opening of 5,6-dihydrouracil to N-carbamyl-alanine and of 5,6-dihydrothymine to N-carbamyl-amino isobutyrate.Tissue specificity:Liver and kidney.Involvement in disease:Defects in DPYS are the cause of dihydropyrimidinase deficiency (DHPD). DHPD is an autosomal recessive disorder characterized by dihydropyrimidinuria and associated with a variable clinical phenotype: epileptic or convulsive attacks, dysmorphic features and severe developmental delay, and congenital microvillous atrophy.
Image Unavailable-10481-154

Anti-DPYS Rabbit Polyclonal Antibody (Cy7®)

Catalog Number: (10481-154)
Supplier: Bioss
Description: Catalyzes the second step of the reductive pyrimidine degradation, the reversible hydrolytic ring opening of dihydropyrimidines. Can catalyzes the ring opening of 5,6-dihydrouracil to N-carbamyl-alanine and of 5,6-dihydrothymine to N-carbamyl-amino isobutyrate.Tissue specificity:Liver and kidney.Involvement in disease:Defects in DPYS are the cause of dihydropyrimidinase deficiency (DHPD). DHPD is an autosomal recessive disorder characterized by dihydropyrimidinuria and associated with a variable clinical phenotype: epileptic or convulsive attacks, dysmorphic features and severe developmental delay, and congenital microvillous atrophy.
Image Unavailable-76108-478

Anti-Dihydropyrimidinase Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalog Number: (76108-478)
Supplier: Bioss
Description: Catalyzes the second step of the reductive pyrimidine degradation, the reversible hydrolytic ring opening of dihydropyrimidines. Can catalyzes the ring opening of 5,6-dihydrouracil to N-carbamyl-alanine and of 5,6-dihydrothymine to N-carbamyl-amino isobutyrate.Tissue specificity:Liver and kidney.Involvement in disease:Defects in DPYS are the cause of dihydropyrimidinase deficiency (DHPD). DHPD is an autosomal recessive disorder characterized by dihydropyrimidinuria and associated with a variable clinical phenotype: epileptic or convulsive attacks, dysmorphic features and severe developmental delay, and congenital microvillous atrophy.
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