benzalphthalide

(E)-3-benzylideneisobenzofuran-1(3H)-one

CAS: 575-61-1 C15 H10 O2 MW: 222.24310000

Identification

Namebenzalphthalide
CAS Number575-61-1
EINECS209-388-8
FDA UNIIC9E8S3AGYQ
Molecular FormulaC15 H10 O2
Molecular Weight222.24310000
MDL NumberMFCD00005929
Beilstein0083797

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Boiling Point 374.10 °C. @ 760.00 mm Hg (est)
Flash Point 314.00 °F. TCC ( 156.90 °C. ) (est)
logP (o/w) 4.270 (est)
Soluble in water, 148.8 mg/L @ 25 °C (est)

Cosmetic Information

CosIngcosmetic data
Cosmetic Usesuv absorbers

No sensory data available

Safety Information

Preferred SDSView
Oral/Parenteral Toxicityintraperitoneal-mouse LD > 500 mg/kg
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categorycosmetic UV absorber
Recommendation for benzalphthalide usage levels up tonot for fragrance use.
Recommendation for benzalphthalide flavor usage levels up tonot for flavor use.

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Potential Uses

u.v. absorbers

Natural Occurrence

not found in nature

Synonyms

benzal phthalide 1(3H)-I\iso benzofuranane, 3-(phenylmethylene)- 1(3H)-iso benzofuranone, 3-(phenylmethylene)-, (3E)- 3- benzylidene phthalide (3E)-3- benzylidene-2-benzofuran-1-one (3E)-3- benzylidene-2-benzofuran-1(3H)-one (E)-3- benzylideneisobenzofuran-1(3H)-one 3- benzylidenphthalide 3-[1- phenyl-meth-(E)-ylidene]-3H-isobenzofuran-1-one PubMed: Bacterial degradation of benzalphthalide. PubMed: Metabolism of benzalphthalide by Pseudomonas sp. PubMed: Identification and quantitation of a 3-benzylidenephthalide contaminant of phenindione tablets and its characterization as a potentially immunogenic substance. PubMed: One-step synthesis of isocoumarins and 3-benzylidenephthalides via ligandless Pd-catalyzed oxidative coupling of benzoic acids and vinylarenes. PubMed: Synthesis of 3-substituted isocoumarins and their inhibitory effects on degranulation of RBL-2H3 cells induced by antigen. PubMed: Anti-HIV activity of stilbene-related heterocyclic compounds.