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96109

Supelco

Anisole

analytical standard

Sinonimo/i:

Methoxybenzene, Methyl phenyl ether

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About This Item

Formula condensata:
CH3OC6H5
Numero CAS:
100-66-3
Peso molecolare:
108.14
Beilstein:
506892
Numero CE:
202-876-1
Numero MDL:
MFCD00008354
Codice UNSPSC:
41116107
eCl@ss:
39023603
ID PubChem:
329770490
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Densità del vapore

3.7 (vs air)

Tensione di vapore

10 mmHg ( 42.2 °C)

Saggio

≥99.9% (GC)

Temp. autoaccensione

887 °F

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Indice di rifrazione

n20/D 1.516 (lit.)
n20/D 1.518

P. eboll.

154 °C (lit.)

Punto di fusione

−37 °C (lit.)

Densità

0.995 g/mL at 25 °C (lit.)

applicazioni

cleaning products
cosmetics
environmental
flavors and fragrances
food and beverages
personal care

Formato

neat

Stringa SMILE

COc1ccccc1

InChI

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

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Descrizione generale

Anisole is a colorless liquid , which can be obtained upon heating anisic acid with an excess of barium hydroxide.

Applicazioni

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pittogrammi

FlameExclamation mark
GHS02,GHS07

Avvertenze

Warning

Indicazioni di pericolo

H226,H336

Classi di pericolo

Flam. Liq. 3 - STOT SE 3

Organi bersaglio

Central nervous system

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

109.4 °F - closed cup

Punto d’infiammabilità (°C)

43 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificati d'analisi (COA)

Lot/Batch Number
BCCG1642
BCCC9646
BCCB4538
BCBW7678
BCBV6956

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Elements of Chemistry: Including the History of the Imponderables and the Inorganic Chemistry (1846)
Practical Organic Chemistry (1975)
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
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