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| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 1 g | Check Cart for Availability | $1,510.00 |
About This Item
Linear Formula:
CH315NH2·HCl
CAS Number:
Molecular Weight:
68.51
NACRES:
NA.12
PubChem Substance ID:
UNSPSC Code:
12352116
MDL number:
Isotopic purity:
98 atom % 15N
Mass shift:
M+1
Form:
solid
isotopic purity
98 atom % 15N
Quality Level
form
solid
mp
232-234 °C (lit.)
mass shift
M+1
SMILES string
Cl.C[15NH2]
InChI
1S/CH5N.ClH/c1-2;/h2H2,1H3;1H/i2+1;
InChI key
NQMRYBIKMRVZLB-CGOMOMTCSA-N
Packaging
This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.
1 of 1
This Item | |||
|---|---|---|---|
| isotopic purity 98 atom % 15N | isotopic purity 99 atom % 13C, 99 atom % D | isotopic purity 99 atom % 13C | isotopic purity 98 atom % 15N |
| mass shift M+1 | mass shift M+4 | mass shift M+1 | mass shift M+1 |
| Quality Level 200 | Quality Level 200 | Quality Level 200 | Quality Level 200 |
| form solid | form solid | form solid | form solid |
| mp 232-234 °C (lit.) | mp 232-234 °C (lit.) | mp 232-234 °C (lit.) | mp 227-230 °C (lit.) |
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Thomas S Hofer et al.
Molecular bioSystems, 8(11), 2891-2900 (2012-08-01)
Molecular dynamics simulations have been performed to investigate the binding of tris(hydroxymethyl)-aminomethane to the surface of the core domain of the mouse cellular tumor antigen p53 employing the GROMOS and 53A6 force field parameter sets. A close investigation of the
April D Lewoczko et al.
Physical chemistry chemical physics : PCCP, 15(13), 4707-4714 (2013-02-21)
Using density functional theory calculations, we report on the adsorption of methylamine on gold and compare its adsorption to a selection of alkylamines, methanol and methanethiol. On the (111) surface, the amines, thiol and alcohol bind in the ontop site
Alejandro Cruz et al.
Molecules (Basel, Switzerland), 17(9), 10178-10191 (2012-08-28)
Symmetric and non-symmetric 2-(N-H, N-methyl, N-ethylenyl and N-aryl)guanidinebenzothiazoles were synthesized from the reaction of ammonia, methylamine, pyrrolidine and aniline with dimethyl benzo[d]thiazol-2-yl-carbonodithioimidate as intermediate. The products were characterized by ¹H-, ¹³C-NMR spectroscopy and three of them by X-ray diffraction analysis.
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 490288-1G | 04061826239971 |




