Iniciar sesión para ver los precios por organización y contrato.
Seleccione un Tamaño
Cambiar Vistas
Acerca de este artículo
Fórmula empírica (notación de Hill):
C7H5NO4
Número CAS:
Peso molecular:
167.12
UNSPSC Code:
23151817
eCl@ss:
39151816
PubChem Substance ID:
NACRES:
NB.21
MDL number:
Servicio técnico
¿Necesita ayuda? Nuestro equipo de científicos experimentados está aquí para ayudarle.
Permítanos ayudarledescription
anionic
Quality Level
concentration
0.02 M C7H5NO4 in water (0.04N)
technique(s)
ion chromatography: suitable
SMILES string
OC(=O)c1cccc(n1)C(O)=O
InChI
1S/C7H5NO4/c9-6(10)4-2-1-3-5(8-4)7(11)12/h1-3H,(H,9,10)(H,11,12)
InChI key
WJJMNDUMQPNECX-UHFFFAOYSA-N
General description
This eluent concentrate for ion chromatography is determined by potentiometric titration. Content and expiry date can be found on the certificate.
Application
Preparation Note
Prepared with 2,6-pyridinecarboxylic acid and high purity water (18.2 MΩ, 0.2 μm filtered)
Other Notes
Visit the IC Portal to learn more
Clase de almacenamiento
10 - Combustible liquids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
Elija entre una de las versiones más recientes:
¿Ya tiene este producto?
Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.
Chao Xu et al.
Inorganic chemistry, 52(5), 2750-2756 (2013-02-21)
Complexation of UO2(2+) with dipicolinic acid (DPA) has been investigated in 0.1 M NaClO4. The stability constants (log β1 and log β2) for two successive complexes, UO2L and UO2L2(2-) where L(2-) stands for the deprotonated dipicolinate anion, were determined to
C C J van Melis et al.
International journal of food microbiology, 160(2), 124-130 (2012-11-28)
In this study, the impact of a range of organic acids and structurally similar alcohols with three to six carbon backbones and increasing lipophilic character, were tested on the germination behavior of B. cereus ATCC 14579 spores. This approach allowed
Development of metal-chelating inhibitors for the Class II fructose 1,6-bisphosphate (FBP) aldolase.
Geneviève Labbé et al.
Journal of inorganic biochemistry, 112, 49-58 (2012-05-02)
It has long been suggested that the essential and ubiquitous enzyme fructose 1,6-bisphosphate (FBP) aldolase could be a good drug target against bacteria and fungi, since lower organisms possess a metal-dependant (Class II) FBP aldolase, as opposed to higher organisms