Skip to Content
Merck
All Photos(1)

Documents

UC260

Sigma-Aldrich

Carboxytolbutamide

Synonym(s):

N-Butyl-N´-(4-carboxyphenylsulfonyl)urea

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C12H16N2O5S
CAS Number:
2224-10-4
Molecular Weight:
300.33
MDL number:
MFCD00272697
UNSPSC Code:
12161501
PubChem Substance ID:
329827662
NACRES:
NA.77

form

solid

color

white

mp

210-212 °C

solubility

methanol: soluble

storage temp.

2-8°C

SMILES string

CCCCNC(=O)NS(=O)(=O)c1ccc(cc1)C(O)=O

InChI

1S/C12H16N2O5S/c1-2-3-8-13-12(17)14-20(18,19)10-6-4-9(5-7-10)11(15)16/h4-7H,2-3,8H2,1H3,(H,15,16)(H2,13,14,17)

InChI key

GCMVATDSSHTCOS-UHFFFAOYSA-N

Application

Carboxytolbutamide has been used as a standard to determine tolbutamide metabolites in urine samples.

Biochem/physiol Actions

In vivo tolbutamide metabolite. Major urinary metabolite of tolbutamide.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Preparation Note

Carboxytolbutamide is soluble in methanol.

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H318

Precautionary Statements

P280 - P305 + P351 + P338

Hazard Classifications

Eye Dam. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

M A Bruce et al.
Drug metabolism and disposition: the biological fate of chemicals, 29(7), 1023-1028 (2001-06-16)
The in vivo effects of oral clarithromycin administration on the in vivo activity of cytochrome P450 1A2, 2C9, and 2D6 were determined. The cytochrome P450 probes caffeine (CYP1A2), tolbutamide (CYP2C9), and dextromethorphan (CYP2D6) were administered as an oral cocktail prior
E W Cate et al.
Journal of clinical pharmacology, 26(5), 372-377 (1986-05-01)
This study was designed to compare the effects of equivalent therapeutic doses of two H2 antagonists, cimetidine and ranitidine, on tolbutamide pharmacokinetics. Twelve healthy men were given a 1-g oral dose of tolbutamide on three occasions. Subjects were randomly assigned
T Y Nelson et al.
The Journal of biological chemistry, 262(6), 2608-2612 (1987-02-25)
The mechanisms by which glyburide and tolbutamide signal insulin secretion were examined using a beta cell line (Hamster insulin-secreting tumor (HIT) cells). Insulin secretion was measured in static incubations, free cytosolic Ca2+ concentration ([Ca2+]i) was monitored in quin 2-loaded cells
G A Cook
The Journal of biological chemistry, 262(11), 4968-4972 (1987-04-15)
The hypoglycemic sulfonylureas glyburide and tolbutamide were found to be excellent inhibitors of the rat liver, heart, and skeletal muscle carnitine palmitoyltransferases, but glyburide was by far the most potent inhibitor. Carboxytolbutamide, a sulfonylurea that has no hypoglycemic effect, produced
Joanne C Krupa et al.
The Biochemical journal, 361(Pt 3), 613-619 (2002-01-23)
The ability of the lysosomal cysteine protease cathepsin B to function as a peptidyldipeptidase (removing C-terminal dipeptides) has been attributed to the presence of two histidine residues (His(110) and His(111)) present in the occluding loop, an extra peptide segment located
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service