All Photos(3)
About This Item
Linear Formula:
[(HO)2C6H3]2CO
CAS Number:
Molecular Weight:
246.22
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
97%
mp
198-200 °C (lit.)
SMILES string
Oc1ccc(c(O)c1)C(=O)c2ccc(O)cc2O
InChI
1S/C13H10O5/c14-7-1-3-9(11(16)5-7)13(18)10-4-2-8(15)6-12(10)17/h1-6,14-17H
InChI key
WXNRYSGJLQFHBR-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
Related Categories
Application
- Urinary concentrations of bisphenol A, parabens and benzophenone-type ultra violet light filters in relation to sperm DNA fragmentation in young men: A chemical mixtures approach.: This study investigates the relationship between urinary concentrations of various chemicals, including benzophenone-type UV filters like 2,2′,4,4′-Tetrahydroxybenzophenone, and sperm DNA fragmentation. The findings highlight potential reproductive toxicity risks associated with exposure to these compounds (Kiwitt-Cárdenas et al., 2024).
- Salting-out assisted liquid-liquid extraction combined with LC-MS/MS for the simultaneous determination of seven organic UV filters in environmental water samples: method development and application.: This paper discusses the development of a method for detecting organic UV filters, including 2,2′,4,4′-Tetrahydroxybenzophenone, in environmental water samples. The method offers a reliable way to monitor the presence of these compounds in the environment (Carve et al., 2023).
- Novel visible-light-active P-g-CN-based α-Bi(2)O(3)/WO(3) ternary photocatalysts with a dual Z-scheme heterostructure for the efficient decomposition of refractory ultraviolet filters and environmental hormones: Benzophenones.: The study presents a new photocatalyst capable of degrading benzophenone-type UV filters, including 2,2′,4,4′-Tetrahydroxybenzophenone, under visible light. This development has significant implications for environmental cleanup technologies (Berekute et al., 2023).
- Boosting elimination of sunscreen, Tetrahydroxybenzophenone (BP-2), from water using monopersulfate activated by thorny NanoBox of Co@C prepared via the engineered etching strategy: A comparative and mechanistic investigation.: This research explores a novel method for removing 2,2′,4,4′-Tetrahydroxybenzophenone from water using advanced nanotechnology, highlighting its effectiveness and potential for environmental applications (Khiem et al., 2023).
- The binding mechanism of benzophenone-type UV filters and human serum albumin: The role of site, number, and type of functional group substitutions.: The study examines how benzophenone-type UV filters, including 2,2′,4,4′-Tetrahydroxybenzophenone, interact with human serum albumin, providing insights into their behavior in biological systems and potential health implications (Ma et al., 2023).
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Sens. 1A
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
Christin J Weisbrod et al.
Toxicology and applied pharmacology, 225(3), 255-266 (2007-09-25)
The UV filter benzophenone-2 (BP-2) is largely used in personal care products such as cosmetics and in numerous other materials for UV protection. Like other UV filters, BP-2 has been found to be estrogenic in vitro and in vivo, but
Armin Zenker et al.
Journal of chromatography. A, 1202(1), 64-74 (2008-07-18)
A new sensitive method has been successfully developed and validated for the simultaneous determination and quantification of nine estrogenic UV filters (benzophenone-1, benzophenone-2, benzophenone-3, benzophenone-4, 4,4-dihydroxybenzophenone, ethyl-4-aminobenzoate, 2-ethyl-hexyl-4-trimethoxycinnamate, 3-(4-methylbenzylidene)-camphor, 3-benzylidene-camphor) in different environmental matrices. After optimisation of extraction conditions for
Christiane Schlecht et al.
Toxicology, 205(1-2), 123-130 (2004-10-02)
The estrogen receptors (ERs) are members of a super family of ligand-activated transcription factors mediating estrogenic responses. A close functional kinship was found for the structurally related estrogen receptor-related receptor1 (ERR1), a constitutively active transcription factor. The aryl hydrocarbon receptor
Hubertus Jarry et al.
Toxicology, 205(1-2), 87-93 (2004-10-02)
The chemical industry has developed sun protection factor products, which contain a variety of so-called "UV screens", among others, benzophenones (BP). Based on the structure it can be assumed, that the variant BP2 may be a potent estrogenic endocrine disrupter
Michael H Hsieh et al.
The Journal of urology, 178(4 Pt 2), 1637-1642 (2007-08-21)
Additives such as benzophenone-2 are commonly used in cosmetic products and food container plastics to filter out ultraviolet light. In pregnant women exposure may result in transplacental transfer of benzophenone-2 to fetuses. Benzophenone-2 is estrogenic in vitro and in the
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service