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Key Documents

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P19809

Sigma-Aldrich

2-Phenylbenzimidazole

97%

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About This Item

Fórmula empírica (notación de Hill):
C13H10N2
Número de CAS:
716-79-0
Peso molecular:
194.23
EC Number:
211-939-2
MDL number:
MFCD00005592
UNSPSC Code:
12352100
eCl@ss:
32151902
PubChem Substance ID:
24898258
NACRES:
NA.22

Quality Level

100

assay

97%

form

solid

mp

293-296 °C (lit.)

SMILES string

c1ccc(cc1)-c2nc3ccccc3[nH]2

InChI

1S/C13H10N2/c1-2-6-10(7-3-1)13-14-11-8-4-5-9-12(11)15-13/h1-9H,(H,14,15)

InChI key

DWYHDSLIWMUSOO-UHFFFAOYSA-N

Gene Information

human ... FGFR1(2260) , PDGFRB(5159)

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pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
STBJ5725
STBJ5724
S41869
S34691
04811PC

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Yukio Kubota et al.
Nucleic acids research. Supplement (2001), (2)(2), 193-194 (2003-08-09)
We have studied the influence of terminal substituents, amidinium group and N-methylpiperazine ring, of 2-phenylbenzimidazole compounds (1-6; Figure 1) on their DNA-binding modes. Experimental results reveal that 1-3 are accepted in intercalation pockets owing to structural flexibility of the N-methylpiperazine
Mehrorang Ghaedi et al.
Journal of hazardous materials, 158(1), 131-136 (2008-03-04)
A new and efficient solid phase extraction method is described for the preconcentration of trace heavy metal ions. The method is based on the adsorption of Fe(3+), Cu(2+) and Zn(2+) on 2-phenyl-1H-benzo[d] imidazole (PHBI) loaded on Triton X-100-coated polyvinyl chloride
Charity N Mosley et al.
International journal of environmental research and public health, 4(2), 126-131 (2007-07-10)
2-phenylbenzimidazole (PBI) is an ingredient found in sunscreen agents. PBI can absorb the UV portion of the solar light and undergo a series of light-induced reactions to cause adverse effects in humans. Therefore, chemical and photochemical toxicity of PBI were
Mark L Richards et al.
European journal of medicinal chemistry, 41(8), 950-969 (2006-05-02)
The pharmacotherapy of allergy and asthma has traditionally focused on the effecter molecules of the allergic cascade, while neglecting targets that play an early role in their development. Reasoning that IgE is central to the expansion of atopic diseases, we
C Stevenson et al.
Chemical research in toxicology, 12(1), 38-45 (1999-01-20)
Gel sequencing experiments with end-labeled synthetic oligodeoxyribonucleotides have established that 2-phenylbenzimidazole (PBZ) and the common sunscreen constituent 2-phenylbenzimidazole-5-sulfonic acid (PBSA) function as efficient photosensitizers of DNA damage when they are exposed to UV-B (290-320 nm) radiation or natural sunlight. Although
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