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Key Documents

64785

Sigma-Aldrich

4-Methoxybenzamidine

suitable for fluorescence, ≥96.0% (NT)

Synonym(s):

4-Amidinoanisole

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About This Item

Empirical Formula (Hill Notation):
C8H10N2O
CAS Number:
Molecular Weight:
150.18
Beilstein/REAXYS Number:
637173
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:

assay

≥96.0% (NT)

mp

119-124 °C

fluorescence

λex 393 nm; λem 478 nm (after derivatization with glucose)
λex 393 nm; λem 478 nm(lit.)

suitability

suitable for fluorescence

SMILES string

COc1ccc(cc1)C(N)=N

InChI

1S/C8H10N2O/c1-11-7-4-2-6(3-5-7)8(9)10/h2-5H,1H3,(H3,9,10)

InChI key

CSISQILZUHMAJB-UHFFFAOYSA-N

Application

Reagent for the determination of reducing carbohydrates and glycoproteins by postcolumn derivatization after HPLC; A method using benzamidine should be improved by this reagent

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Skin Corr. 1B

Storage Class

8B - Non-combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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M. Kai et al.
Analytical Sciences, 1, 59-59 (1985)
A. Coquet et al.
Chromatographia, 34, 651-651 (1992)
H.J.C. Nells et al.
Analytical Chemistry, 54, 213-213 (1982)
Zhang, G.Q., et al.
Analytical Sciences, 9, 9-9 (1993)
E Farcaş et al.
Talanta, 188, 516-521 (2018-07-22)
Capillary electrophoresis (CE) instrument was used for the generation of a robust and reliable nanoreactor for enzymatic assays in the context of antithrombotic drug screening. The activity of the screened molecules was monitored in a quick and fully automated fashion

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