All Photos(1)
About This Item
Linear Formula:
CH3C6H4N=NNHCH3
CAS Number:
Molecular Weight:
149.19
Beilstein:
1841442
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
98%
form
solid
mp
75-80 °C (lit.)
SMILES string
CNN=Nc1ccc(C)cc1
InChI
1S/C8H11N3/c1-7-3-5-8(6-4-7)10-11-9-2/h3-6H,1-2H3,(H,9,10)
InChI key
DNGJVDGPCGXBFF-UHFFFAOYSA-N
Application
3-Methyl-1-(p-tolyl)triazene was used for methylation during simultaneous determination of hippuric and o-, m- and p-methylhippuric acids by gas chromatography.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Carc. 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
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.
J R Caperos et al.
British journal of industrial medicine, 34(3), 229-233 (1977-08-01)
A gas chromatographic method for simultaneous determination of hippuric and o-, m-, and p-methylhippuric acids (metabolites of toluene and xylene) in urine is described. The analytical procedure is based on the extraction of the aromatic metabolites with ethyl acetate containing
Yoshiaki Miura et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 13(17), 4797-4804 (2007-03-21)
A rapid and quantitative method for solid-phase methyl esterification of carboxy groups of various sialylated oligosaccharides has been established. The method employed a triazene derivative, 3-methyl-1-p-tolyltriazene, for facile derivatization of oligosaccharides immobilized onto general solid supports such as Affi-Gel Hz
Hidenori Takahashi et al.
Oncology reports, 44(6), 2757-2769 (2020-10-31)
The N‑glycoforms of glycoproteins modify protein function and control a number of biological pathways. The aim of the present study was to investigate the correlation between alterations in N‑glycans and cancer aggressiveness in terms of cancer cell invasion ability. The
Abrha G Gebrehiwot et al.
PloS one, 13(12), e0209515-e0209515 (2018-12-29)
Most glycomics studies have focused on understanding disease mechanisms and proposing serum markers for various diseases, yet the influence of ethnic variation on the identified glyco-biomarker remains poorly addressed. This study aimed to investigate the inter-ethnic serum N-glycan variation among
Motamed Elsayed Mahmoud et al.
Molecular biology reports, 46(3), 2733-2748 (2019-03-28)
Glycosylation is a post-translational protein modification in eukaryotes and plays an important role in controlling several diseases. N-glycan structure is emerging as a new paradigm for biomarker discovery of neuropsychiatric disorders. However, the relationship between N-glycosylation pattern and depression is
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