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T7891

Supelco

Thiochrom

analytical standard

Synonym(e):

2,7-Dimethylthiachromin-8-ethanol

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About This Item

Empirische Formel (Hill-System):
C12H14N4OS
CAS-Nummer:
92-35-3
Molekulargewicht:
262.33
EG-Nummer:
202-149-9
MDL-Nummer:
MFCD00010519
UNSPSC-Code:
41116107
PubChem Substanz-ID:
24900483
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

100

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

forensics and toxicology
pharmaceutical (small molecule)

Format

neat

SMILES String

Cc1ncc2CN3C(C)=C(CCO)SC3=Nc2n1

InChI

1S/C12H14N4OS/c1-7-10(3-4-17)18-12-15-11-9(6-16(7)12)5-13-8(2)14-11/h5,17H,3-4,6H2,1-2H3

InChIKey

GTQXMAIXVFLYKF-UHFFFAOYSA-N

Anwendung

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

Biochem./physiol. Wirkung

Selektiver M4 Muscarinrezeptor verstärkt Acetylcholin-Affinität.

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
MKCP8562
MKCN5957
MKCK6850
MKCF9552
MKCC9853

Die passende Version wird nicht angezeigt?

Wenn Sie eine bestimmte Version benötigen, können Sie anhand der Lot- oder Chargennummer nach einem spezifischen Zertifikat suchen.

Suche nach COA

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Pteroinsäure ≥93%

Sigma-Aldrich

P1781

Pteroinsäure

2-Furaldehyd analytical standard

Supelco

04623

2-Furaldehyd

L-Cystein BioUltra, ≥98.5% (RT)

Sigma-Aldrich

30089

L-Cystein

Retinol synthetic, ≥95% (HPLC), (Powder or Powder with Lumps)

Sigma-Aldrich

R7632

Retinol

2-Furaldehyd 99%

Sigma-Aldrich

185914

2-Furaldehyd

Thiamin -hydrochlorid reagent grade, ≥99% (HPLC)

Sigma-Aldrich

T4625

Thiamin -hydrochlorid

Benzalkoniumchlorid ≥95.0% ((calculated on dry substance), T)

Sigma-Aldrich

12060

Benzalkoniumchlorid

A Floridi et al.
International journal for vitamin and nutrition research. Internationale Zeitschrift fur Vitamin- und Ernahrungsforschung. Journal international de vitaminologie et de nutrition, 54(2-3), 165-171 (1984-01-01)
A sensitive method for the measurement of thiamine pyrophosphate in whole blood and erythrocytes, using a straight-phase high performance liquid chromatography (HPLC), is described. The method was based on sample extraction with trichloracetic acid, conversion of the vitamer to the
F S Larin et al.
Ukrainskii biokhimicheskii zhurnal (1978), 58(5), 89-91 (1986-09-01)
Thiochrome caproate modified by the oxyethyl radical of the thiochrome derivative was studied for its effect on different indices of lipid metabolism in the liver and blood of albino rats. It was shown that when animals were fed on a
Sung Joon Ahn et al.
The international journal of biochemistry & cell biology, 35(2), 157-167 (2002-12-14)
Effects of the coenzyme thiamine pyrophosphate and its analogs on the inhibition of self-splicing of primary transcripts of the phage T4 thymidylate synthase gene (td) were investigated. Of all compounds tested, the coenzyme thiamine pyrophosphate was the most potent inhibitor
J Schrijver et al.
Annals of clinical biochemistry, 19(Pt 1), 52-56 (1982-01-01)
A sensitive and reliable method for the determination of total thiamine (vitamin B1) in whole blood has been developed which is suited for routine analysis. After extraction, and enzymatic hydrolysis of thiamine phosphate esters, thiamine is separated from interfering compounds
Hailin Zhu et al.
Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 19(2), 289-294 (2003-03-01)
Fluorometric determination of thiamine requires the conversion of the analyte to fluorescent thiochrome by hexacyanoferrate(III) oxidation in alkaline solution and the isolation of the produced thiochrome from the reaction medium by solvent extraction. It was observed that thiochrome could be
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