5-Benzoyl-4-hydroxy-2-methoxybenzenesulfonic acid

Name: 5-Benzoyl-4-hydroxy-2-methoxybenzenesulfonic acid
Brand: SIAL
Price: 126 USD

≥97.0% (HPLC)

Synonym(s):

HMBS, Sulisobenzone

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10 G

$126.00

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About This Item

Empirical Formula (Hill Notation):

C₁₄H₁₂O₆S

CAS Number:

4065-45-6

Molecular Weight:

308.31

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

329748781

EC Number:

223-772-2

Beilstein/REAXYS Number:

2889165

MDL number:

MFCD00024962

Assay:

≥97.0% (HPLC)

Form:

powder

Key Documents

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InChI key

CXVGEDCSTKKODG-UHFFFAOYSA-N

InChI

1S/C14H12O6S/c1-20-12-8-11(15)10(7-13(12)21(17,18)19)14(16)9-5-3-2-4-6-9/h2-8,15H,1H3,(H,17,18,19)

SMILES string

COc1cc(O)c(cc1S(O)(=O)=O)C(=O)c2ccccc2

assay

≥97.0% (HPLC)

form

powder

impurities

≤10% water

functional group

ketone, phenyl, sulfonic acid

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This Item	52619	8.51042	M2786
Sigma-Aldrich 09649 5-Benzoyl-4-hydroxy-2-methoxybenzenesulfonic acid	Supelco 52619 Hexamethyldisilazane	Sigma-Aldrich 8.51042 HMBA	Sigma-Aldrich M2786 3-Maleimidobenzoic acid N-hydroxysuccinimide ester
assay ≥97.0% (HPLC)	assay ≥99.0% (GC)	assay ≥98% (TLC)	assay -
form powder	form liquid	form powder	form crystalline
impurities ≤10% water	impurities -	impurities -	impurities -
functional group ketone	functional group -	functional group -	functional group NHS ester, maleimide

pictograms

GHS07

signalword

Warning

hcodes

H315,H319,H412

pcodes

P264 - P273 - P280 - P302 + P352 - P305 + P351 + P338 - P332 + P313

Hazard Classifications

Aquatic Chronic 3 - Eye Irrit. 2 - Skin Irrit. 2

Storage Class

11 - Combustible Solids

wgk

WGK 1

flash_point_f

No data available

flash_point_c

No data available

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number

0000451636

0000426021

0000237737

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Photodegradation of (-)-epigallocatechin-3-gallate in topical cream formulations and its photostabilization.

Anna Bianchi et al.

Journal of pharmaceutical and biomedical analysis, 56(4), 692-697 (2011-08-03)

The aim of the study was to examine the photostability of the major catechin of green tea, (-)-epigallocatechin-3-gallate (EGCG), which possesses important antioxidant and skin photoprotective properties. In order to simulate realistic conditions of use of topical preparations, the photolysis

UVA/UVB sunscreen determination by second-order derivative ultraviolet spectrophotometry.

J S Azevedo et al.

Farmaco (Societa chimica italiana : 1989), 54(9), 573-578 (1999-11-11)

UVA/UVB protective agents are important constituents in many cosmetics and sunscreen preparations. Analytical methodologies which enable the determination of combined substances with different spectrophotometric characteristics are therefore useful and cost-effective. To this end, the following substances in a sunscreen gel

Reactive oxygen species assay-based risk assessment of drug-induced phototoxicity: classification criteria and application to drug candidates.

Satomi Onoue et al.

Journal of pharmaceutical and biomedical analysis, 47(4-5), 967-972 (2008-05-06)

We have previously demonstrated that the phototoxic potential of chemicals could be partly predicted by the determination of reactive oxygen species (ROS) from photo-irradiated compounds. In this study, ROS assay strategy was applied to 39 marketed drugs and 210 drug

A reversed-phase ion-interaction chromatographic method for in-vitro estimation of the percutaneous absorption of water-soluble UV filters.

Z León et al.

Analytical and bioanalytical chemistry, 391(3), 859-866 (2008-03-28)

An analytical method based on ion-interaction chromatography with UV detection for simultaneous in-vitro estimation of the percutaneous absorption of the most used water-soluble UV filters in sunscreen cosmetics is proposed. These UV filters were phenylbenzimidazole sulfonic acid, disodium phenyl dibenzimidazole

Effects of ethylene glycol monomethyl ether and its metabolite, 2-methoxyacetic acid, on organogenesis stage mouse limbs in vitro.

Caroline Dayan et al.

Birth defects research. Part B, Developmental and reproductive toxicology, 101(3), 254-261 (2014-05-07)

Exposure to ethylene glycol monomethyl ether (EGME), a glycol ether compound found in numerous industrial products, or to its active metabolite, 2-methoxyacetic acid (2-MAA), increases the incidence of developmental defects. Using an in vitro limb bud culture system, we tested

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5-Benzoyl-4-hydroxy-2-methoxybenzenesulfonic acid