T45802
2,4,6-Triaminopyrimidine
97%
Synonym(s):
2,4,6-Pyrimidinetriamine
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About This Item
Empirical Formula (Hill Notation):
C4H7N5
CAS Number:
Molecular Weight:
125.13
Beilstein:
118448
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
97%
mp
249-251 °C (lit.)
SMILES string
Nc1cc(N)nc(N)n1
InChI
1S/C4H7N5/c5-2-1-3(6)9-4(7)8-2/h1H,(H6,5,6,7,8,9)
InChI key
JTTIOYHBNXDJOD-UHFFFAOYSA-N
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Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
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
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J W Jansen et al.
Biochimica et biophysica acta, 598(1), 115-126 (1980-05-08)
1. The permeability of the paracellular pathway in the isolated rabbit pancreas has been studied with the aid of 2,4,6-triaminopyrimidine. 2. Addition of 2,4,6-triaminopyrimidine (1--10 mM) to the bathing medium has no effect on the rate of fluid secretion or
Nicolas Cenac et al.
Journal of immunology (Baltimore, Md. : 1950), 170(8), 4296-4300 (2003-04-19)
Activation of colonic proteinase-activated receptor-2 (PAR-2) provokes colonic inflammation and increases mucosal permeability in mice. The mechanism of inflammation is under debate and could be neurogenic and/or the consequence of tight-junction opening with passage of exogenous pathogens into the lamina
P Y Wong
Experientia, 36(5), 570-571 (1980-05-15)
Intracellular potentials in the cells from 17.5-day old rat visceral yolk sacs were measured by a glass microelectrode. When penetrated from the maternal side, the cells have potentials of about 50.2 +/- 1.9 mV (inside negative) which were reduced by
U Kück-Biere et al.
Gut, 31(1), 64-69 (1990-01-01)
K+ concentrations were measured in vitro with K+ sensitive microelectrodes in the microclimate at the luminal cell surface of the colon of guinea pigs. The serosal K+ concentration was mostly 5.4 mmol/1, the mucosal K+ concentrations were changed (0, 5
Jong Huem Yoon et al.
Organic letters, 7(14), 2889-2892 (2005-07-01)
[reaction: see text] A new recyclable supported catalyst system for orthoalkylation was devised using a self-assembly consisting of the barbiturate and 2,4,6-triaminopyrimidine H-bonding motifs. At high temperature, the system is completely homogeneous so as to give an efficient catalytic activity
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