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126217

Sigma-Aldrich

2,4-Dihydroxybenzophenone

99%

Sinónimos:

DHB

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About This Item

Fórmula lineal:
(HO)2C6H3COC6H5
Número de CAS:
131-56-6
Peso molecular:
214.22
Beilstein/REAXYS Number:
1311566
EC Number:
205-029-4
MDL number:
MFCD00002277
UNSPSC Code:
12162002
PubChem Substance ID:
24847708
NACRES:
NA.23

assay

99%

form

powder

mp

144.5-147 °C (lit.)

SMILES string

Oc1ccc(c(O)c1)C(=O)c2ccccc2

InChI

1S/C13H10O3/c14-10-6-7-11(12(15)8-10)13(16)9-4-2-1-3-5-9/h1-8,14-15H

InChI key

ZXDDPOHVAMWLBH-UHFFFAOYSA-N

Gene Information

rat ... Ar(24208)

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Categorías relacionadas

Application


  • Substituent Effects on the Ultraviolet Absorption Properties of 2, 4-Dihydroxy Dibenzophenone: This research examines how different substituents affect the UV absorption characteristics of 2,4-dihydroxybenzophenone, a compound important for its UV protective properties (Wu et al., 2022).

  • Kevlar® and Nomex modification via 2, 4-dihydroxybenzophenone anchoring improves water repellency and induces antibacterial and UV protection properties: Explores the enhancement of Kevlar and Nomex fabrics by anchoring 2,4-dihydroxybenzophenone to improve their functional properties (Tonis et al., 2023).

Legal Information

Kevlar is a registered trademark of E. I. du Pont de Nemours and Company

signalword

Warning

Hazard Classifications

Aquatic Chronic 2 - Eye Irrit. 2 - Repr. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

257.0 °F

flash_point_c

125 °C

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Ting-Hao Kuo et al.
Analytica chimica acta, 1080, 95-103 (2019-08-15)
Structural analysis of biomolecules is essential to natural product discovery, especially for precious biomaterials such as agarwood. However, one of the greatest challenges to the characterization of natural products is the profound cost in time and manpower to the structural
Kresten Ole Kusk et al.
Environmental toxicology and chemistry, 30(4), 959-966 (2011-01-05)
Benzophenone (BP)-type ultraviolet (UV) filters are widely used in cosmetic and sunscreen products and can enter the aquatic environment. Therefore, we investigated the subchronic toxicity of 2,4-dihydroxybenzophenone (BP1) on the marine calanoid copepod Acartia tonsa in an early life-stage development
Min-Ah Park et al.
Toxicology, 305, 41-48 (2013-01-19)
2,4-Dihydroxybenzophenone (benzophenone-1; BP-1) is an UV stabilizer primarily used to prevent polymer degradation and deterioration in quality due to UV irradiation. Recently, BP-1 has been reported to bioaccumulate in human bodies by absorption through the skin and has the potential
L Fredriksen et al.
Applied and environmental microbiology, 85(6) (2019-01-13)
A two-domain GH10 xylanase-encoding gene (amor_gh10a) was discovered from a metagenomic data set, generated after in situ incubation of a lignocellulosic substrate in hot sediments on the sea floor of the Arctic Mid-Ocean Ridge (AMOR). AMOR_GH10A comprises a signal peptide
Natalie C Bamford et al.
Nature communications, 11(1), 2450-2450 (2020-05-18)
The exopolysaccharide galactosaminogalactan (GAG) is an important virulence factor of the fungal pathogen Aspergillus fumigatus. Deletion of a gene encoding a putative deacetylase, Agd3, leads to defects in GAG deacetylation, biofilm formation, and virulence. Here, we show that Agd3 deacetylates
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