Skip to Content
Merck
All Photos(3)

Documents

214698

Sigma-Aldrich

Pyridinium dichromate

98%

Synonym(s):

PDC

Sign Into View Organizational & Contract Pricing
All Photos(3)

About This Item

Empirical Formula (Hill Notation):
C10H10N2 · H2Cr2O7
CAS Number:
20039-37-6
Molecular Weight:
376.20
EC Number:
243-478-8
MDL number:
MFCD00013105
UNSPSC Code:
12352005
PubChem Substance ID:
24852846
NACRES:
NA.22

Assay

98%

form

solid

reaction suitability

reagent type: oxidant

mp

152-153 °C (lit.)

SMILES string

c1ccncc1.c2ccncc2.O[Cr](=O)(=O)O[Cr](O)(=O)=O

InChI

1S/2C5H5N.2Cr.2H2O.5O/c2*1-2-4-6-5-3-1;;;;;;;;;/h2*1-5H;;;2*1H2;;;;;/q;;2*+1;;;;;;;/p-2

InChI key

RCBVKBFIWMOMHF-UHFFFAOYSA-L

Looking for similar products? Visit Product Comparison Guide

General description

Pyridinium dichromate is a pyridinium salt and strong oxidizing agent to convert primary alcohols and secondary alcohols to aldehydes and ketones respectively.

Application

Oxidizing agent for conversion of primary alcohols to aldehydes and ketones, acetals to esters, and didehydroketones to enones in the presence of tert-butyl hydroperoxide (cat. no. 213128).

Signal Word

Danger

Hazard Statements

H228,H314,H317,H350i,H410

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1B Inhalation - Eye Dam. 1 - Flam. Sol. 1 - Skin Corr. 1B - Skin Sens. 1

Storage Class Code

4.1A - Other explosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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

Yihui Zhou et al.
Environmental pollution (Barking, Essex : 1987), 219, 932-938 (2016-10-07)
In this study, polybrominated diphenyl ethers (PBDEs) and methoxylated polybrominated diphenyl ethers (MeO-PBDEs) were analyzed in eleven freshwater fish species from Dianshan Lake, Shanghai, China. The highest concentrations of PBDEs and MeO-PBDEs were found in snakehead, with mean values of
J. Mol. Catal. A: Chem., 250, 70-70 (2006)
K M Halkes et al.
Carbohydrate research, 309(2), 161-174 (1998-09-19)
To contribute to the possibilities to study the ability of oligosaccharide fragments of hyaluronic acid to induce angiogenesis, several hyaluronic-acid-related oligosaccharides and their 6-O-sulfated analogues were synthesised as their 4-methoxyphenyl glycosides having 2-acetamido-2-deoxy-D-glucopyranose at the reducing end. In all syntheses
Yong-Hua Li et al.
Epilepsy research, 128, 149-157 (2016-11-14)
Localization of the epileptogenic zone (EZ) is essential for the successful surgical treatment of medically intractable epilepsy. In the present study, stereo-EEG (SEEG) recordings were obtained from seven patients underwent presurgical evaluation for treatment of intractable epilepsy. Partial directed coherence
Mark Hanly et al.
Paediatric and perinatal epidemiology, 32(1), 114-125 (2017-11-23)
Preterm birth and developmental vulnerability are more common in Australian Aboriginal compared with non-Aboriginal children. We quantified how gestational age relates to developmental vulnerability in both populations. Perinatal datasets were linked to the Australian Early Development Census (AEDC), which collects
View All Related Papers

Articles

Oxidizing and Reducing Agents

Oxidation and reduction reactions are some of the most common transformations encountered in organic synthesis

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