21861
1,1′-Carbonyl-di-(1,2,4-triazole)
technical, ≥90% (T)
Synonym(s):
CDT
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Recommended Products
grade
technical
Quality Level
Assay
≥90% (T)
form
powder
reaction suitability
reaction type: Carbonylations
mp
138-152 °C
application(s)
peptide synthesis
storage temp.
2-8°C
SMILES string
O=C(n1cncn1)n2cncn2
InChI
1S/C5H4N6O/c12-5(10-3-6-1-8-10)11-4-7-2-9-11/h1-4H
InChI key
YHNUDLCUIKMNSN-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
Other Notes
Reagent for preparing the reactive acyl triazolides from carboxylic acids; Reaction of unprotected glucose with acyl triazolide to the β-D-glucosyl ester; Dehydrating agent which reacts with H2O2 giving singlet oxygen, used e.g. for epoxidations
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Repr. 2
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
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
Helvetica Chimica Acta, 63, 277-277 (1980)
Journal of the American Geriatrics Society, 66(7), 1360-1366 (2018-05-11)
To investigate the implications of obtaining one or more low scores on a battery of cognitive tests on diagnosing mild cognitive impairment (MCI). Observational longitudinal study. Alzheimer's Disease Neuroimaging Initiative. Normal controls (NC, n = 280) and participants with MCI
Anaerobe, 60, 102083-102083 (2019-08-05)
The relevance of large clostridial toxin-negative, binary toxin-producing (A-B-CDT+) Clostridium difficile strains in human infection is still controversial. In this study, we investigated putative virulence traits that may contribute to the role of A-B-CDT+C. difficile strains in idiopathic diarrhea. Phenotypic assays
European journal of human genetics : EJHG, 23(6), 808-816 (2014-11-06)
Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant muscular disorder with a wide clinical variability. Contractions of the D4Z4 macrosatellite repeat on chromosome 4q35 are the molecular basis of the pathophysiology. Recently, in a subset of patients without D4Z4 repeat
PloS one, 12(8), e0184030-e0184030 (2017-08-31)
Imprinted genes show parent-specific activity (functional haploidy), which makes them particularly vulnerable to epigenetic dysregulation. Here we studied the methylation profiles of oppositely imprinted genes at single DNA molecule resolution by two independent parental allele-specific deep bisulfite sequencing (DBS) techniques.
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