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PHR1419

Supelco

Sulfanilic Acid

Pharmaceutical Secondary Standard; Certified Reference Material

Synonyme(s) :

Sulfanilic acid, 4-Aminobenzenesulfonic acid, Aniline-4-sulfonic acid

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About This Item

Formule linéaire :
4-(H2N)C6H4SO3H
Numéro CAS:
Poids moléculaire :
173.19
Numéro Beilstein :
908765
Numéro CE :
Numéro MDL:
Code UNSPSC :
41116107
ID de substance PubChem :
Nomenclature NACRES :
NA.24

Qualité

certified reference material
pharmaceutical secondary standard

Niveau de qualité

Agence

traceable to USP 1633506

Famille d'API

sulfadimethoxine, sulfadiazine, mesalazine

CofA (certificat d'analyse)

current certificate can be downloaded

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Pf

>300 °C (lit.)

Application(s)

pharmaceutical (small molecule)

Format

neat

Température de stockage

2-30°C

Chaîne SMILES 

Nc1ccc(cc1)S(O)(=O)=O

InChI

1S/C6H7NO3S/c7-5-1-3-6(4-2-5)11(8,9)10/h1-4H,7H2,(H,8,9,10)

Clé InChI

HVBSAKJJOYLTQU-UHFFFAOYSA-N

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Description générale

Sulfanilic Acid is a synthetic organic compound, obtained via sulfonation of aniline with sulfuric acid. It is widely used for the production of optical brightening agents, synthetic organic dyes, food colorants and additives.

Application

These Secondary Standards are qualified as Certified Reference Materials. These are suitable for use in several analytical applications including but not limited to pharma release testing, pharma method development for qualitative and quantitative analyses, food and beverage quality control testing, and other calibration requirements.

Note de bas de page

To see an example of a Certificate of Analysis for this material enter LRAC3847 in the slot below. This is an example certificate only and may not be the lot that you receive.

Produits recommandés

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Produit(s) apparenté(s)

Réf. du produit
Description
Tarif

Pictogrammes

Exclamation mark

Mention d'avertissement

Warning

Mentions de danger

Classification des risques

Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1

Code de la classe de stockage

13 - Non Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


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Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

Luís Belo et al.
PloS one, 9(6), e98467-e98467 (2014-06-06)
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Virginia A Pereira et al.
Malaria journal, 14, 30-30 (2015-01-30)
Cytokines play an important role in human immune responses to malaria and variation in their production may influence the course of infection and determine the outcome of the disease. The differential production of cytokines has been linked to single nucleotide
Aminul Islam et al.
Journal of AOAC International, 98(1), 165-175 (2015-04-11)
Amberlite® XAD-16 was functionalized with p-aminobenzene sulfonic acid via an azo spacer in order to prepare a new chelating resin, which was then characterized by water regain value, hydrogen ion capacity, elemental analyses, and IR spectral and thermal studies. The
Kraingkrai Ponhong et al.
Talanta, 133, 71-76 (2014-12-02)
A novel four-channel simultaneous injection effective mixing flow analysis (SIEMA) system has been assembled for successive determination of bilirubin and creatinine in urinary samples. The chemical variables and physical parameters in the flow system were optimized for the enhancement of
Ming-Wei Chao et al.
Toxicological sciences : an official journal of the Society of Toxicology, 141(1), 300-313 (2014-06-29)
Epidemiological studies have demonstrated extensive human exposure to the monocyclic aromatic amines, particularly to 3,5-dimethylaniline, and found an association between exposure to these compounds and risk for bladder cancer. Little is known about molecular mechanisms that might lead to the

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