139335
3-Methyl-1-(p-tolyl)triazene
98%
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About This Item
Linear Formula:
CH3C6H4N=NNHCH3
CAS Number:
Molecular Weight:
149.19
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
244-223-3
Beilstein/REAXYS Number:
1841442
MDL number:
Assay:
98%
Form:
solid
Product Name
3-Methyl-1-(p-tolyl)triazene, 98%
InChI key
DNGJVDGPCGXBFF-UHFFFAOYSA-N
InChI
1S/C8H11N3/c1-7-3-5-8(6-4-7)10-11-9-2/h3-6H,1-2H3,(H,9,10)
SMILES string
CNN=Nc1ccc(C)cc1
assay
98%
form
solid
mp
75-80 °C (lit.)
functional group
amine
Quality Level
Related Categories
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.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Carc. 2
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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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
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
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
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
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
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