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126217

2,4-Dihydroxybenzophenone

Name: 2,4-Dihydroxybenzophenone
Brand: ALDRICH

99%

Synonym(s):

DHB

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About This Item

Linear Formula:

(HO)₂C₆H₃COC₆H₅

CAS Number:

131-56-6

Molecular Weight:

214.22

UNSPSC Code:

12162002

NACRES:

NA.23

PubChem Substance ID:

24847708

EC Number:

205-029-4

Beilstein/REAXYS Number:

1311566

MDL number:

MFCD00002277

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Properties

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)

Description

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

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pictograms

GHS08,GHS07,GHS09

signalword

Warning

hcodes

H319,H361fd,H411

pcodes

P202 - P264 - P273 - P280 - P305 + P351 + P338 - P308 + P313

Hazard Classifications

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

Storage Class

11 - Combustible Solids

wgk

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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Effect of 2,4-dihydroxybenzophenone (BP1) on early life-stage development of the marine copepod Acartia tonsa at different temperatures and salinities.

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

Mass spectrometry imaging guided molecular networking to expedite discovery and structural analysis of agarwood natural products.

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

Benzophenone-1 stimulated the growth of BG-1 ovarian cancer cells by cell cycle regulation via an estrogen receptor alpha-mediated signaling pathway in cellular and xenograft mouse models.

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

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Global Trade Item Number

SKU	GTIN
126217-100G	04061838723932