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2-Amino-3-methylbenzoic acid

$58

  • Brand : BIOFRON

  • Catalogue Number : BN-O1171

  • Specification : 98%(HPLC)

  • CAS number : 4389-45-1

  • Formula : C8H9NO2

  • Molecular Weight : 151.16

  • PUBCHEM ID : 78101

  • Volume : 5mg

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Catalogue Number

BN-O1171

Analysis Method

Specification

98%(HPLC)

Storage

2-8°C

Molecular Weight

151.16

Appearance

Botanical Source

Structure Type

Category

SMILES

CC1=C(C(=CC=C1)C(=O)O)N

Synonyms

2-Amino-3-methylbenzoic acid/3-Methylanthranilic acid/2-Amino-m-toluic Acid/2-Amino-3-methylbenzoicacid/Benzoic acid, 2-amino-3-methyl-/2-Amino-3-methyl benzoicacid

IUPAC Name

2-amino-3-methylbenzoic acid

Density

1.3±0.1 g/cm3

Solubility

Flash Point

144.4±24.6 °C

Boiling Point

315.1±30.0 °C at 760 mmHg

Melting Point

174-177 °C(lit.)

InChl

InChl Key

WNAJXPYVTFYEST-UHFFFAOYSA-N

WGK Germany

RID/ADR

HS Code Reference

Personal Projective Equipment

Correct Usage

For Reference Standard and R&D, Not for Human Use Directly.

Meta Tag

provides coniferyl ferulate(CAS#:4389-45-1) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Articles of coniferyl ferulate are included as well.>> amp version: coniferyl ferulate

No Technical Documents Available For This Product.

PMID

3751122

Abstract

Metabolism of lidocaine in rabbit liver 9000 g supernatant fraction was examined. A capillary g.l.c. assay was developed to separate seven known metabolites of lidocaine, and all seven metabolites were identified in extracts of incubations of lidocaine with rabbit-liver fractions. These metabolites were monoethylglycinexylidide(I), glycinexylidide(II), 3-hydroxymonoethylglycinexylidide(III), 3-hydroxylidocaine(IV), 4-hydroxylidocaine(V), xylidine(VI) and 4-hydroxyxylidine(VII). A new metabolite, 2-amino-3-methylbenzoic acid(VIII), was identified in extracts of incubations of lidocaine with rabbit-liver fractions, by comparison of the mass-spectral fragmentation patterns and g.l.c. retention time with those of the authentic compound. The formation of VIII is dependent on protein, NADPH, time, O2, and the presence of soluble enzymes. Quantitative analysis of metabolites I-VIII after a two hour incubation accounts for 89% of the metabolized lidocaine.

Title

Lidocaine Metabolism by Rabbit-Liver Homogenate and Detection of a New Metabolite

Author

R C Kammerer, D A Schmitz

Publish date

1986 Jul;

PMID

15002967

Abstract

The design, synthesis, characterization, and screening of a large, encoded thiazolidinone library are described. Three sets of 35 building blocks were combined by encoded split-pool synthesis to give a library containing more than 42 000 members. Building block selection was based in part on a novel small molecule follicle stimulating hormone receptor agonist hit and in part for diversity. HPLC/MS techniques were applied at the single-bead level to build confidence in the reliability of library construction. Application of two distinct screening strategies resulted in the identification of compounds with significantly improved potency over the initial hit. This work demonstrates the versatility of encoded libraries for preparing a large number of analogues of a given hit while simultaneously generating a large collection of compounds for screening against other targets.

Title

Agonists of the Follicle Stimulating Hormone Receptor From an Encoded Thiazolidinone Library

Author

Derek Maclean 1, Frank Holden, Ann M Davis, Randall A Scheuerman, Stephen Yanofsky, Christopher P Holmes, William L Fitch, Ken Tsutsui, Ronald W Barrett, Mark A Gallop

Publish date

Mar-Apr 2004


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