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70356-09-1

70356-09-1 structure
70356-09-1 structure
  • Name: Avobenzone
  • Chemical Name: 1-(4-tert-Butylphenyl)-3-(4-methoxyphenyl)-1,3-propanedione
  • CAS Number: 70356-09-1
  • Molecular Formula: C20H22O3
  • Molecular Weight: 310.387
  • Catalog: Catalysts and additives UV absorber
  • Create Date: 2018-02-10 08:00:00
  • Modify Date: 2024-01-02 11:48:41
  • Avobenzone is an oil soluble ingredient used in sunscreen products to absorb the full spectrum of UVA rays and a dibenzoylmethane derivative.Target: OthersAvobenzone is an oil soluble ingredient used in sunscreen products to absorb the full spectrum of UVA rays and a dibenzoylmethane derivative. It can degrade faster in light in combination with mineral UV absorbers like zinc oxide and titanium dioxide, though with the right coating of the mineral particles this reaction can be reduced. A manganese doped titanium dioxide may be better than undoped titanium dioxide to improve avobenzone's stability. It reacts with minerals to form colored complexes. Manufacturers of avobenzone, like DSM recommend to include a chelator to prevent this from happening. They also recommend to avoid the inclusion of iron and ferric salts, heavy metals, formaldehyde donors and PABA and PABA esters[1].

Name 1-(4-tert-Butylphenyl)-3-(4-methoxyphenyl)-1,3-propanedione
Synonyms 1-[4-(1,1-Dimethylethyl)phenyl]-3-(4-methoxyphenyl)-1,3-propanedione
MFCD00210252
1-(4-tert-Butylphenyl)-3-(4-methoxyphenyl)propane-1,3-dione
1,3-Propanedione, 1-[4-(1,1-dimethylethyl)phenyl]-3-(4-methoxyphenyl)-
4-tert-Butyl-4'-methoxydibenzoylmethane
Avobenzone
1-(4-Methoxyphenyl)-3-[4-(2-methyl-2-propanyl)phenyl]-1,3-propanedione
1X1&1&R DV1VR DO1
EINECS 274-581-6
Avobenzone (USP)
Description Avobenzone is an oil soluble ingredient used in sunscreen products to absorb the full spectrum of UVA rays and a dibenzoylmethane derivative.Target: OthersAvobenzone is an oil soluble ingredient used in sunscreen products to absorb the full spectrum of UVA rays and a dibenzoylmethane derivative. It can degrade faster in light in combination with mineral UV absorbers like zinc oxide and titanium dioxide, though with the right coating of the mineral particles this reaction can be reduced. A manganese doped titanium dioxide may be better than undoped titanium dioxide to improve avobenzone's stability. It reacts with minerals to form colored complexes. Manufacturers of avobenzone, like DSM recommend to include a chelator to prevent this from happening. They also recommend to avoid the inclusion of iron and ferric salts, heavy metals, formaldehyde donors and PABA and PABA esters[1].
Related Catalog
References

[1]. Singh, P. and O.H. Nautiyal, Synthesis of Parsol [4-(1, 1-Dimethylethyl)-4'-methoxydibenzoylmethane)]. Asian Journal of Research in Chemistry, 2011. 4(11).

Density 1.1±0.1 g/cm3
Boiling Point 463.6±35.0 °C at 760 mmHg
Melting Point 81-84 °C
Molecular Formula C20H22O3
Molecular Weight 310.387
Flash Point 203.1±26.0 °C
Exact Mass 310.156891
PSA 43.37000
LogP 4.81
Vapour Pressure 0.0±1.1 mmHg at 25°C
Index of Refraction 1.545
Symbol GHS09
GHS09
Signal Word Warning
Hazard Statements H410
Precautionary Statements P273-P501
Personal Protective Equipment Eyeshields;Gloves
Hazard Codes N
Risk Phrases R50/53
Safety Phrases S60-S61
RIDADR UN3077 9/PG 3
HS Code 29145000

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Literature: DSM IP ASSETS B.V.; WEHRLI, Christof Patent: WO2012/84770 A1, 2012 ; Location in patent: Page/Page column 8-9 ;

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Literature: DSM IP ASSETS B.V.; WEHRLI, Christof Patent: WO2012/84770 A1, 2012 ; Location in patent: Page/Page column 10-11 ;

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Literature: US2013/58879 A1, ; Paragraph 0194 ;

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Literature: Journal de Chimie Physique et de Physico-Chimie Biologique, , vol. 95, # 2 p. 388 - 394

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Literature: Journal of Photochemistry and Photobiology A: Chemistry, , vol. 209, # 2-3 p. 153 - 157

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Literature: RSC Advances, , vol. 3, # 43 p. 19785 - 19788
HS Code 2909499000
Summary 2909499000. ether-alcohols and their halogenated, sulphonated, nitrated or nitrosated derivatives. VAT:17.0%. Tax rebate rate:9.0%. . MFN tariff:5.5%. General tariff:30.0%