Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

705128

Sigma-Aldrich

Resorufin-d6

98 atom % D, 96% (CP)

Synonym(s):

7-Hydroxy-3H-phenoxazin-3-one-d6

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C12D6HNO3
CAS Number:
1196157-65-9
Molecular Weight:
219.23
MDL number:
MFCD11656671
UNSPSC Code:
12352005
PubChem Substance ID:
329762505
NACRES:
NA.24

isotopic purity

98 atom % D

Assay

96% (CP)

form

powder

technique(s)

mass spectrometry (MS): suitable

mp

>300 °C

mass shift

M+6

storage temp.

−20°C

SMILES string

[2H]c1c([2H])c2N=C3C([2H])=C([2H])C(=O)C([2H])=C3Oc2c([2H])c1O

InChI

1S/C12H7NO3/c14-7-1-3-9-11(5-7)16-12-6-8(15)2-4-10(12)13-9/h1-6,14H/i1D,2D,3D,4D,5D,6D

InChI key

HSSLDCABUXLXKM-MZWXYZOWSA-N

Packaging

This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MBBC1235
MBBB9559V
MBBB8610V
MBBB7753V
MBBB7708V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Devaraj Venkatapura Chandrashekar et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 1153, 122272-122272 (2020-08-02)
Ethoxyresorufin (ER)-O-deethylation (EROD) activity has been widely used to assess cytochrome P450 1A (CYP1A) activity. The kinetics of CYP1A activity have been well characterized in the liver microsomes. However, studies in kidney microsomes are limited due to the much lower
Jade Huguet et al.
Xenobiotica; the fate of foreign compounds in biological systems, 49(2), 187-199 (2018-02-17)
1. The objective of our study was to develop and validate a cocktail approach to allow the simultaneous characterization of various CYP450-mediated oxidations by human heart microsomes for nine probe drug substrates, namely, 7-ethoxyresorufin, bupropion, repaglinide, tolbutamide, bufuralol, chlorzoxazone, ebastine

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service