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About This Item
Linear Formula:
2-(C6H5NH)C6H4CO2H
CAS Number:
Molecular Weight:
213.23
EC Number:
202-066-8
UNSPSC Code:
12352200
PubChem Substance ID:
Beilstein/REAXYS Number:
1456607
MDL number:
grade
technical
assay
≥95% (T)
form
powder
mp
182-185 °C
application(s)
peptide synthesis
SMILES string
OC(=O)c1ccccc1Nc2ccccc2
InChI
1S/C13H11NO2/c15-13(16)11-8-4-5-9-12(11)14-10-6-2-1-3-7-10/h1-9,14H,(H,15,16)
InChI key
ZWJINEZUASEZBH-UHFFFAOYSA-N
Gene Information
human ... TTR(7276)
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Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Walter E Finkbeiner et al.
American journal of physiology. Lung cellular and molecular physiology, 301(4), L402-L414 (2011-07-05)
We investigated how cystic fibrosis (CF) alters the relationship between Cl(-) and mucin secretion in cultures of non-CF and CF human tracheobronchial gland mucous (HTGM and CFTGM, respectively) cells. Biochemical studies showed that HTMG cells secreted typical airway mucins, and
Henrique B Silva et al.
Journal of cellular physiology, 223(1), 244-251 (2010-01-06)
The bone marrow stromal cell line S17 has been used to study hematopoiesis in vitro. In this study, we demonstrate the presence of calcium and chloride currents in cultured S17 cells. Calcium currents were of low amplitude or barely detectable
Marie-Claire Michoud et al.
American journal of respiratory cell and molecular biology, 40(2), 217-222 (2008-09-02)
Patients with cystic fibrosis (CF) suffer from asthma-like symptoms and gastrointestinal cramps, attributed to a mutation in the CF transmembrane conductance regulator (CFTR) gene present in a variety of cells. Pulmonary manifestations of the disease include the production of thickened