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50194

Supelco

Sulisobenzone

analytical standard

Sinonimo/i:

5-Benzoyl-4-hydroxy-2-methoxybenzenesulfonic acid, HMBS, Sulisobenzone

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About This Item

Formula empirica (notazione di Hill):
C14H12O6S
Numero CAS:
4065-45-6
Peso molecolare:
308.31
Beilstein:
2889165
Numero CE:
223-772-2
Numero MDL:
MFCD00024962
Codice UNSPSC:
41116107
ID PubChem:
329757575
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Saggio

≥97.5% (HPLC)

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

cleaning products
cosmetics
environmental
food and beverages
personal care

Formato

neat

Stringa SMILE

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

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)
CXVGEDCSTKKODG-UHFFFAOYSA-N

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Descrizione generale

Sulisobenzone is a broad spectrum organic UV filter in sunscreen formulations, known to absorb deleterious UV light.

Applicazioni

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Sulisobenzone may be used as an analytical reagent for the determination of the analyte in sunscreen formulations by high-performance liquid chromatography with UV spectrophotometric detection.

Confezionamento

Bottomless glass bottle. Contents are inside inserted fused cone.

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H315,H319,H412

Classi di pericolo

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

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

No data available

Punto d’infiammabilità (°C)

No data available

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Certificati d'analisi (COA)

Lot/Batch Number
BGBC3807V
BGBC3806V
BGBC3805V
BGBC3804V
BCBH0992V

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Determination of UV-filters in sunscreens by HPLC.
Chisvert A, et al.
Fresenius Journal of Analytical Chemistry, 369(7-8), 638-641 (2001)
S M Edwards et al.
Photodermatology, photoimmunology & photomedicine, 10(3), 111-117 (1994-06-01)
The ability to accurately predict the phototoxic potential of personal and skin care products remains a key element in assessing the safety of premarketed products. To find a reliable in vitro alternative test for photoirritancy, the European Commission and the
M Jarratt et al.
Journal of the American Academy of Dermatology, 9(3), 354-360 (1983-09-01)
A PABA ester-oxybenzone preparation is superior to PABA or sulisobenzone alone in protecting the skin from methoxsalen-induced ultraviolet A (UVA) phototoxicity after water substantivity challenge. Such a mixture would be useful as a UVA screen for uninvolved or actinically damaged
C Augustin et al.
Photodermatology, photoimmunology & photomedicine, 13(1-2), 27-36 (1997-02-01)
Phototoxicity inducing in vivo photoirritation, a reversible inflammatory reaction of the skin after chemical contact and UVA radiation exposure, is increasingly observed as a side effect associated with the use of both cosmetics and systemic drugs. In order to systematically
Zacarías León et al.
Analytica chimica acta, 664(2), 178-184 (2010-04-07)
2-Hydroxy-4-methoxybenzophenone and 2-hydroxy-4-methoxybenzophenone-5-sulphonic acid, commonly known as benzophenone-3 (BZ3) and benzophenone-4 (BZ4), respectively, are substances widely used as UV filters in cosmetic products in order to absorb UV radiation and protect human skin from direct exposure to the deleterious wavelengths
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