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Key Documents

Altri documenti

328022

Sigma-Aldrich

4-Methylhippuric acid

98%

Sinonimo/i:

N-(4-Methylbenzoyl)glycine, p-Toluric acid

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About This Item

Formula condensata:
CH3C6H4CONHCH2CO2H
Numero CAS:
27115-50-0
Peso molecolare:
193.20
Numero CE:
248-231-8
Numero MDL:
MFCD00020449
Codice UNSPSC:
12352100
ID PubChem:
24859708
NACRES:
NA.22

Livello qualitativo

100

Saggio

98%

Forma fisica

powder

Punto di fusione

163-165 °C (lit.)

Stringa SMILE

Cc1ccc(cc1)C(=O)NCC(O)=O

InChI

1S/C10H11NO3/c1-7-2-4-8(5-3-7)10(14)11-6-9(12)13/h2-5H,6H2,1H3,(H,11,14)(H,12,13)
NRSCPTLHWVWLLH-UHFFFAOYSA-N

Categorie correlate

Descrizione generale

4-Methylhippuric acid is the major metabolite of xylene and has been determined in urine by gas chromatography.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

Certificati d'analisi (COA)

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Hippuric acid for synthesis

Sigma-Aldrich

8.20649

Hippuric acid

(R)-(−)-Mandelic acid 98%

Sigma-Aldrich

M2209

(R)-(−)-Mandelic acid

Sodium formate analytical standard

Supelco

67253

Sodium formate

o-Cresol analytical standard

Supelco

36922

o-Cresol

2,5-Hexanedione ≥98%

Sigma-Aldrich

165131

2,5-Hexanedione

(R)-(−)-Mandelic acid ReagentPlus®, ≥99%

Sigma-Aldrich

154210

(R)-(−)-Mandelic acid

Peter T Mayer et al.
Journal of pharmaceutical sciences, 91(3), 640-646 (2002-03-29)
The barrier domain solubility-diffusion theory of lipid bilayer permeability relates the permeability coefficient (P(m)) to the solute's partition coefficient (PC(barrier/w)) and diffusion coefficient (D(barrier)) in the ordered chain region of the bilayer that serves as the barrier region for polar
Measurement of exposure to xylenes by separate determination of m- and p-methylhippuric acids in urine.
M Morin et al.
Journal of chromatography, 210(2), 346-349 (1981-06-05)
G Bieniek et al.
British journal of industrial medicine, 38(3), 304-306 (1981-08-01)
The separation of hippuric and m-methylhippuric acid as toluene and m-xylene metabolites present in urine of people exposed simultaneously to toluene and xylene is described. Chloroform was used for hippuric and m-methylhippuric acid extraction. Satisfactory separation of these metabolites was
P T Mayer et al.
AAPS pharmSci, 2(2), E14-E14 (2001-12-14)
To explore the independence of functional group contributions to permeability of nonelectrolytes across egg lecithin bilayers, the transport rates were measured of a series of alpha-substituted p-methylhippuric acids (-H, -Cl, -OCH3, -CN, -OH, -COOH, and -CONH2) across egg lecithin lipid
T X Xiang et al.
The Journal of membrane biology, 177(2), 137-148 (2000-09-26)
The influence of varying concentrations of a transmembrane peptide, gramicidin A (gA), and cholesterol (Chol) on the passive permeation of p-methylhippuric acid (MHA) and alpha-carbamoyl-p-methylhippuric acid (CMHA) across egg-lecithin membranes (EPC) has been investigated in vesicle efflux experiments. Incorporation of
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