Detail of > 76656-36-5
- CAS Number:
- 76656-36-5
- Name:
Benzenesulfonic acid,3,3'-carbonylbis[4-hydroxy-6-methoxy-, sodium salt (1:2)
- Superlist Name:
- Disodium 2,2'-dihydroxy-4,4'-dimethoxy-5,5'-disulfobenzophenone
- Formula:
- C15H12Na2O11S2
- Molecular Structure:

- Synonyms:
- Benzenesulfonicacid, 3,3'-carbonylbis[4-hydroxy-6-methoxy-, disodium salt (9CI);Benzophenone9;Uvinul 3048;Uvinul DS 49;
- Molecular Weight:
- 478.35
- EINECS:
- 278-520-4
- Melting Point:
- 350 °C (dec.)
- Deleted CAS:
- 64719-73-9
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Reference
- Thermal recording material with good lightfastness
- Thermal recording material with good lightfastness.Some chemicals with cas registry numbers like 4065-45-6 and 76656-36-5 are also used. Ogino, Naomi; Oomori, Takashi; Ueda, Hiroshi; Myake, Sumio; Midorikawa, Yoshimi; Wakita, Yutaka (Nippon Seishi Kk, Japan). Jpn. Kokai Tokkyo Koho JP 09020075 A2 21 Jan 1997 Heisei, 9 pp. (Japanese). (Japan). CODEN: JKXXAF. CLASS: ICM: B41M005-26. ICS: B41M005-30. APPLICATION: JP 1995-170581 6 Jul 1995. DOCUMENT TYPE: Patent CA Section: 74 (Radiation Chemistry, Photochemistry, and Photographic and Other Reprographic Processes) The material comprises a support with coatings of a heat-sensitive layer contg. 2,4-dimethyl-6-[(4-dimethylamino)anilino]fluoran as a leuco dye precursor and a color developer and a protective layer contg. a binder, a water-sol. UV absorbent, a fluorescent dye, and Al(OH)3. The material provides high d. images and backgrounds with good lightfastness and thermal resistance. .
- The potential carcinogenic effect of Uvinul DS49 - a common UV absorber used in cosmetics
- The potential carcinogenic effect of Uvinul DS49 - a common UV absorber used in cosmetics. Bolton, K.; Martincigh, B.Several substances are used for example 65-71-4 and 76656-36-5 which are their cas registry numbers. S.; Salter, L. F. (Dep. Chem. Appl. Chem., Univ. Natal, Durban 4001, S. Afr.). J. Photochem. Photobiol., A, 63(2), 241-8 (English) 1992. CODEN: JPPCEJ. ISSN: 1010-6030. DOCUMENT TYPE: Journal CA Section: 22 (Physical Organic Chemistry) The photosensitized prodn. of thymine dimer at 324 nm was investigated using disodium-2,2-dihydroxy-4,4'-dimethoxybenzophenonesulfonic acid (tradename, Uvinul DS49) as a sensitizer. Yields of the dimer for various irradn. times, initial thymine concns., and initial sensitizer concns. were detd. for the free thyime base in aq. medium. A reaction mechanism is proposed for total thymine dimer formation together with the rate consts. The mechanism and rate consts. were computer simulated to support their validity. .
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