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Merck
CN

PHR1212

苯甲醚

Pharmaceutical Secondary Standard; Certified Reference Material

别名:

甲基苯基醚, 甲氧基苯

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线性分子式:
CH3OC6H5
化学文摘社编号:
分子量:
108.14
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
202-876-1
Beilstein/REAXYS Number:
506892
MDL number:
eCl@ss:
39023603
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InChI key

RDOXTESZEPMUJZ-UHFFFAOYSA-N

InChI

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

SMILES string

COc1ccccc1

grade

certified reference material, pharmaceutical secondary standard

agency

traceable to USP 1037011

vapor density

3.7 (vs air)

vapor pressure

10 mmHg ( 42.2 °C)

CofA

current certificate can be downloaded

autoignition temp.

887 °F

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

refractive index

n20/D 1.516 (lit.)

bp

154 °C (lit.)

mp

−37 °C (lit.)

density

0.995 g/mL at 25 °C (lit.)

application(s)

pharmaceutical (small molecule)

format

neat

storage temp.

2-30°C

Quality Level

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General description

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.
Anisole can be used as a reference standard for the determination of analyte in methoxsalen drug substance.

Other Notes

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.
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.

pictograms

FlameExclamation mark

signalword

Warning

hcodes

Hazard Classifications

Flam. Liq. 3 - STOT SE 3

target_organs

Central nervous system

存储类别

3 - Flammable liquids

wgk

WGK 2

flash_point_f

109.4 °F - closed cup

flash_point_c

43 °C - closed cup

法规信息

危险化学品
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Kohji Omata et al.
Journal of combinatorial chemistry, 12(4), 435-444 (2010-05-22)
To study the synergistic effect on the acidity and activity of Si-Al-Zr ternary oxide system, the mixture design of experiments was applied to prepare the ternary oxides by a sol-gel method, and rapid screening on dehydration of isopropanol and Friedel-Crafts
Laszlo Hollosi et al.
Journal of chromatography. A, 1218(1), 23-31 (2010-12-03)
European food legislation defines a set of 16 polycyclic aromatic hydrocarbons (PAHs) as of high concern for human health. The EU set contains structurally very similar PAHs with ring numbers between 4 and 6, and so raises some separation aspects
Xiaohui Jin et al.
Water research, 46(19), 6519-6530 (2012-10-20)
Second-order reaction rate constants of micropollutants with ozone (k(O3)) and hydroxyl radicals (k(OH)) are essential for evaluating their removal efficiencies from water during ozonation and advanced oxidation processes. Kinetic data are unavailable for many of the emerging micropollutants. Twenty-four micropollutants
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
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.

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