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Key Documents

PHR1212

Supelco

Anisole

Pharmaceutical Secondary Standard; Certified Reference Material

Synonyme(s) :

Methoxybenzene, Methyl phenyl ether

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About This Item

Formule linéaire :
CH3OC6H5
Numéro CAS:
Poids moléculaire :
108.14
Numéro Beilstein :
506892
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 1037011

Densité de vapeur

3.7 (vs air)

Pression de vapeur

10 mmHg ( 42.2 °C)

CofA (certificat d'analyse)

current certificate can be downloaded

Température d'inflammation spontanée

887 °F

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Indice de réfraction

n20/D 1.516 (lit.)

Point d'ébullition

154 °C (lit.)

Pf

−37 °C (lit.)

Densité

0.995 g/mL at 25 °C (lit.)

Application(s)

pharmaceutical (small molecule)

Format

neat

Température de stockage

2-30°C

Chaîne SMILES 

COc1ccccc1

InChI

1S/C7H8O/c1-8-7-5-3-2-4-6-7/h2-6H,1H3

Clé InChI

RDOXTESZEPMUJZ-UHFFFAOYSA-N

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Description générale

Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards.
Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards. Anisole is a volatile phenolic flavor compound that is reported to occur in cooked meat. It is obtained upon heating anisic acid with an excess of barium hydroxide.

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.

Autres remarques

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

Note de bas de page

To see an example of a Certificate of Analysis for this material enter LRAA9025 in the slot below. This is an example certificate only and may not be the lot that you receive.

Pictogrammes

FlameExclamation mark

Mention d'avertissement

Warning

Mentions de danger

Classification des risques

Flam. Liq. 3 - STOT SE 3

Organes cibles

Central nervous system

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

109.4 °F - closed cup

Point d'éclair (°C)

43 °C - closed cup


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Certificats d'analyse (COA)

Lot/Batch Number

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Consulter la Bibliothèque de documents

S Rivera et al.
Analytical and bioanalytical chemistry, 400(5), 1339-1346 (2011-03-08)
Various carotenoids were analyzed by ultra-high-pressure liquid chromatography with tandem mass spectrometry detection (UHPLC-MS/MS). Three different techniques to ionize the carotenoids were compared: electrospray ionization (ESI), atmospheric pressure chemical ionization (APCI) and atmospheric pressure photoionization (APPI). For all of the
Zhiyun Du et al.
Organic & biomolecular chemistry, 10(21), 4164-4171 (2012-03-30)
Described in this study is the ability of tetrabutylammonium salts (TBAX) to mediate an efficient mono- or di-demethylation removing one or two out of five aromatic methoxy methyl groups situated in similar chemical microenvironments in a H-bonded macrocyclic aromatic pentamer.
Yumi Makino et al.
Analytical chemistry, 82(4), 1213-1220 (2010-01-29)
A novel fluorimetric method for determining radicals using the natural phenol sesamol as a fluorogenic reagent is reported. In this assay, sesamol was reacted with aqueous radicals to yield one isomer of a sesamol dimer exclusively. The dimer emitted purple
Unusual ipso substitution of diaryliodonium bromides initiated by a single-electron-transfer oxidizing process.
Toshifumi Dohi et al.
Angewandte Chemie (International ed. in English), 49(19), 3334-3337 (2010-04-21)
Fabien Dutertre et al.
Macromolecular rapid communications, 33(9), 753-759 (2012-04-26)
The self-assembly in water of an amphiphilic P(nBMA(50%) -stat-DMAEMA(50%) )(100)-b-PDMAEMA(235) diblock copolymer based on hydrophilic dimethylaminoethylmethacrylate (DMAEMA) units and hydrophobic n-butylmethacrylate (nBMA) ones is reported. DMAEMA units have been incorporated into the hydrophobic block of this copolymer to moderate its

Articles

Butyl methyl ether; Acetic acid; 2-Butanone; Ethyl acetate; Tetrahydrofuran; 1-Butanol; Isopropyl acetate; Heptane; Propyl acetate; 3-Methylbutanol; 4-Methyl-2-pentanone; Isobutyl acetate; Butyl acetate; Dimethyl sulfoxide; Anisole; Cumene

Protocoles

GC Analysis of Class 3 Residual Solvents on SUPELCOWAX® 10

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