Skip to Content
Merck
All Photos(2)

Documents

Safety Information

279609

Sigma-Aldrich

6-Nitroveratraldehyde

technical grade, 80%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
O2NC6H2-3,4-(OCH3)2CHO
CAS Number:
Molecular Weight:
211.17
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

grade

technical grade

Assay

80%

form

solid

mp

131-133 °C (lit.)

SMILES string

COc1cc(C=O)c(cc1OC)[N+]([O-])=O

InChI

1S/C9H9NO5/c1-14-8-3-6(5-11)7(10(12)13)4-9(8)15-2/h3-5H,1-2H3

InChI key

YWSPWKXREVSQCA-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

6-Nitroveratraldehyde has been used in the preparation of:
  • no-carrier-added 6-18F-fluoro-L-dopa, fundamental tracer for cerebral positron emission tomography studies of dopaminergic system in humans
  • o-nitroaryl-bis(5-methylfur-2-yl)methanes, versatile synthons for the synthesis of nitrogen-containing heterocycles

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

279609-BULK:
279609-5G:
279609-VAR:
279609-25G:


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

Customers Also Viewed

An improved synthesis of no-carrier-added (NCA) 6-[18 F] Fluoro-l-DOPA and its remote routine production for PET investigations of dopaminergic systems.
Reddy GN, et al.
Applied Radiation and Isotopes, 44(4), 645-649 (1993)
o-Nitroaryl-bis (5-methylfur-2-yl) methanes as Versatile Synthons for the Synthesis of Nitrogen-Containing Heterocycles.
Butin AV, et al.
Molecules (Basel), 2(4), 62-68 (1997)
Libi Anandi et al.
Journal of cell science, 130(21), 3749-3763 (2017-09-20)
DNA alkylating agents form the first line of cancer chemotherapy. They not only kill cells but also behave as potential carcinogens. MNU, a DNA methylating agent, is well known to induce mammary tumours in rodents. However, the mechanism of tumorigenesis
Tomohiro Furukawa et al.
Cell chemical biology, 27(11), 1396-1409 (2020-09-06)
Aflatoxin contamination of crops is a serious problem worldwide. Utilization of aflatoxin production inhibitors is attractive, as the elucidation of their modes of action contributes to clarifying the mechanism of aflatoxin production. Here, we identified mitochondrial protease ClpP as the
Shiv Gandhi et al.
Cell chemical biology, 27(11), 1410-1424 (2020-09-06)
Rhomboid intramembrane proteases regulate pathophysiological processes, but their targeting in a disease context has never been achieved. We decoded the atypical substrate specificity of malaria rhomboid PfROM4, but found, unexpectedly, that it results from "steric exclusion": PfROM4 and canonical rhomboid

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