2000 mg/kg 4. The following lists represent a selection of UL's ChemADVISOR Regulatory Database, curated for Prospector in Compliance Highlights. 302776-68-7. Drug created at December 03, 2015 16:51 / Updated at January 07, 2021 03:13. FOIA DHHB has an absorption maximum of 354 nm. This information should not be interpreted without the help of a healthcare provider. This report analyzes the Diethylamino Hydroxybenzoyl Hexyl Benzoate production by region/country, and the sales (consumption) by region/country. makes their documentation available in the regions indicated below: Diethylamino Hydroxybenzoyl Hexyl Benzoate is very photostable and provides strong UVA protection. DHHB has excellent photostability and compatibility with other UV absorbers and other cosmetic ingredients. Properties Articles 2 Spectrum Names Biological Activity Chemical & Physical Properties MSDS MSDS (Chinese) Safety Information Customs Articles 2 More Articles Synonyms Chemsrc provides CAS#:302776-68-7 MSDS, density, melting point, boiling point, structure, etc. Diethylamino hydroxybenzoyl hexyl benzoate has an absorption maximum of 354 nm. Diethylamino hydroxybenzoyl hexyl benzoate is a photostable UV-A absorber. Diethylamino hydroxybenzoyl hexyl benzoate (DHHB) as additive to the UV filter avobenzone in cosmetic sunscreen formulations - Evaluation of the photochemical behavior and photostabilizing effect Eur J Pharm Sci. Epub 2012 Dec 20. Are you a distributor who is interested in being listed here? Diethylamino Hydroxybenzoyl Hexyl Benzoate is a new generation, chemical sunscreen agent (not available in the US due to impossible FDA regulations) that's designed for high UVA protection and high photostability. It has a chemical structure similar to the classical benxophoenone drug class, and displays good photostability 1. It is used in concentrations up to 10% in sunscreen products, either alone or in combination with other UV absorbers . Diethylamino hydroxybenzoyl hexyl benzoate absorbs in the UV-A range with the peak at 354 nm 1. Evaluation of nanostructured lipid carriers (NLC) and nanoemulsions as carriers for UV-filters: characterization, in vitro penetration and photostability studies. Data Availability: Limited. Two azobenzene derivatives CAB/ACB as reusable sunscreen: UV absorptive capacity and biosafety evaluation. 1426392. Contact us! 53 - May cause long-term adverse effects in the aquatic environment: Safety Description: 61 - Avoid release to the environment. Sample Ballot For Alamance County Nc, Goo Jit Zu Galaxy Attack, Small Tuneful Bird Crossword Clue 7 Letters, Entry Level Maintenance Technician Salary Near Missouri, Turning Point Church Fort Worth, Smith Machine Bench Press, ">

The present invention relates to sunscreen or daily care composition comprising (i) hexyl 2-[4-(diethylamino)-2-hydroxybenzoyl]benzoate (INCI diethylamino hydroxybenzoyl hexyl benzoate); and (ii) 1-(4-(1,1-dimethylethyl)phenyl)-3-(4-methoxyphenyl)propane-1,3-dione (INCI butyl methoxydibenzoylmethane); and (iii) 2,4-bis-{[4-(2-ethy-hexyoxy)-2-hydroxy]-pheny}-6-(4-methoxypheny)-1,3,5 triazine . MFCI, who has standardized GMP workshop, well-equipped R&D center for products and application, a lab with advanced instruments, as well as intact GMP management system, has been audited and approved by US FDA. INCI Diethylamino Hydroxybenzoyl Hexyl Benzoate: Der Inhaltsstoff Diethylamino Hydroxybenzoyl Hexyl Benzoate ist ein UV-Filter synthetischen Ursprungs. In addition, the energy transfer by Frster mechanism (FRET), which is the most often mechanism responsible for singlet-singlet quenching, is unlikely in this work. Reducing the amount of harmful sunscreen components that reach the reef environment is a high priority and will require hdyroxybenzoyl involvement of governments, reef managers, divers, snorkelers and swimmers, and the tourism . In a rat acute oral toxicity study, median LD50 value was reported to be >2000 mg/kg . Avoid applying on wounded areas. Let us know! One should not drive a vehicle if using the medicine makes you drowsy, dizzy or lowers your blood-pressure extensively. Average mass 397.507 Da. Please enable it to take advantage of the complete set of features! RSC Adv. CAS Number: 302776-68-7 Molecular formula: C24 H31 N O4 IUPAC Name: hexyl 2-[4-(diethylamino)-2-hydroxybenzoyl]benzoate Type of Substance Composition: mono-constituent substance . The molar absorption coefficient of Diethylamino hydroxybenzoyl hexyl benzoate in EtOH at 25C is obtained to be 39 000 mol/dm3/cm at 354 nm. Diethylamino hydroxybenzoyl hexyl benzoate can be analyzed by this reverse phase (RP) HPLC method with simple conditions. Our ingredients are screened for quality, manufacturing process, government regulations, published research, and our own internal ingredient safety databases. eCollection 2018 Apr 9. We do not sell to patients. Diethylamino Hydroxybenzoyl Hexyl Benzoate provides excellent free radicals protection and is ideal for long-lasting sun care and anti-aging face care products. Products supplied by MFCI has been widely used in both domestic and abroad markets. You may choose a language below to continue to this industry or close this dialog above. and transmitted securely. (Diethylamino hydroxybenzoyl hexyl benzoateINCI)UVABASFUvinul A Plus354[1][2] [3] [] Like other UV filters, diethylamino hydroxybenzoyl hexyl benzoate may be subject to photodegradation upon absorption of UV radiation, which results in the compound passing from a ground state to either a singlet or triplet excited state 1. Can be used up to 10% worldwide except for the US (not available there) and Canada. Diethylamino hydroxybenzoyl hexyl benzoate absorbs in the UV-A range with the peak at 354 nm . Upgrade today! , , , GRBOVI GORICA, MALEV OLGA, DOLENC DARKO, KLOBUAR ROBERTA SAUERBORN, CVETKOVI ELIMIRA, CVETKOVI BRUNO, JOVANIEVI BRANIMIR, : ", Synthesis, characterisation and aquatic ecotoxicity of the UV filter hexyl 2-(4-diethylamino-2-hydroxybenzoyl) benzoate (DHHB) and its chlorinated by-products, Method for producing diethylamino hydroxybenzoyl hexyl benzoate, Production process for diethylaminohydroxybenzoylhexyl benzoate, Method for Producing Diethylaminohydroxybenzoyl Hexil Benzoate, A preparing method of diethylamino hydroxybenzoyl hexylbenzoate, Ultraviolet absorbent, composition, cosmetic and process for preparing cosmetic, Method for separating 2- (4 '-diethylamino-2' -hydroxybenzoyl) hexyl benzoate, Method for obtaining crystalline diethylamino hydroxybenzoyl hexyl benzoate, Preparation method of sofosbuvir impurity, High-molecular ultraviolet-screening agent and its production, Process for producing 2- (4-N, N-dialkylamino-2-hydroxybenzoyl) benzoate, Method for the crystallization of 2-(4-n,n-diethyl amino-2-hydroxy benzoyl)-benzoic acid-n-hexyl ester, Innovative manufacturing and crystallization of iosimenol, Physiologically active substance tan-931, its derivatives, their production and use, Production of oxalic acid monoester compound, Use of amino-substituted hydroxybenzophenones as photostable UV filters in cosmetic and pharmaceutical preparations, Use of amino-substituted hydroxybenzophenones as photoprotective agents and stabilizers for nonliving organic materials, especially plastics, polymer dispersions, lacquers and photographic emulsions, Powdered preparations containing a mixture of 2,4,6-trianilino-p- (carbo-2'-ethylhexyl-1'-oxi) -1,3,5-triazine and diethylamino-hydroxybenzoyl-hexyl-benzoate, Ionic liquids and methods for using the same, Aminohydroxybenzophenone derivative, method for producing the same and ultraviolet absorber and skin external preparation using the same, Purification method for adefovir dipivoxil, Novel process for preparation of iopromide, Method for preparing tricyclic derivatives, Novel pyridine derivatives and method for preparation of intermediate compound for producing sulfonylurea herbicides using the same, Novel method for preparing thienopyrimidine compound and intermediates used therein, A process for the preparation of prasugrel hcl salt, N-substituted maleimide purification method, Method for mass-producing sodium taurodeoxycholate, New method for manufacturing pitavastatin hemicalcium using new intermediate, A Concise, Practical Synthesis of the Pyrido [3, 2, 1-i, j] Cinnoline Ring System of Potent DNA Gyrase Inhibitors, Method for producing pyrimidinyl bipyridine compound and intermediate therefor, Method for preparing bosentan monohydrate, novel intermediate used therefor, and method for preparing same, Novel process for preparing thienopyrimidine compound and intermediates used therein, Novel 4-substituted oxazoloquinolinone derivatives, pharmaceutically acceptable salt thereof and pharmaceutical composition for prevention or treatment of allergic diseases including asthma or atopic dermatitis comprising same, Method for producing 3-aryl uracil compound, A method for preparing an intermediate of iopromide, Method for preparing 4,5-diamino-substituted pyrimidine derivative, and novel compound for preparing same, Method for preparing intermediate for synthesis of sphingosine-1-phosphate receptor agonist, Novel method of preparing 4-(4-aminophenyl)-3-morpholinone, Process for the preparation of high purity olanzapine and crystalline form ii thereof, Method for preparing decitabine with improved yield and purity, Ep: the epo has been informed by wipo that ep was designated in this application, Ep: pct application non-entry in european phase. ANQ870JD20. Diethylamino Hydroxybenzoyl Hexyl Benzoate c dng ngoi da trong cc sn phm kem chng nng ha hc c cha Diethylamino Hydroxybenzoyl Hexyl Benzoate. Diethylamino Hydroxybenzoyl Hexyl Benzoate is most often found as ingredient number 7 within an ingredient list. outdoor research women's argon long sleeve tee jo malone wild bluebell basenotes A sample of Global Regulatory & Advisory Lists Reviewed: A sample of Retailer Compliance Lists Reviewed: Make smarter decisions with instant access to industry-specific regulatory content when you upgrade to a premium Prospector account. NEWS & INSIGHTS . [, Couteau C, Chauvet C, Paparis E, Coiffard L: UV filters, ingredients with a recognized anti-inflammatory effect. RxNorm ID. Diethylamino hydroxybenzoyl hexyl benzoate was not shown to be mutagenic, clastogenic, or phototoxic in vitro 4. Ang mga epekto ay possible, ngunit hindi naman palaging mangyayari. 83020-301. Advisory Agencies and Informational Lists. Contact China Manufactory Hebei Mojin Biotechnology Co.,ltd for the product 302776-68-7 Diethylamino Hydroxybenzoyl Hexyl Benzoate. Diethylamino Hydroxybenzoyl Hexyl Benzoate Usage. We're sorry, but the industry you have selected is not currently available in your chosen language. What Are The Side Effects Of Diethylamino hydroxybenzoyl hexyl benzoate? 2-[4-()-2-]INCIDiethylamino Hydroxybenzoyl Hexyl Benzoate . Diethylamino Hydroxybenzoyl Hexyl Benzoate (DHHB) ( Figure 1 D) This is a widely used UVA filter. Avoid applying to the eye area. It is marketed as Uvinul A Plus by BASF. MeSH Diethylamino Hydroxybenzoyl Hexyl Benzoate provides excellent free radicals protection and is ideal for long-lasting sun care and anti-aging face care products. Not Listed. Ang mga sumusunod ay ang mga side-effects na maaaring lumabas sa mga gamot na may Alcohol / Diethylamino Hydroxybenzoyl Hexyl Benzoate Ito ay hindi isang kumpletong listahan. Diethylamino hydroxybenzoyl hexyl benzoate (DHHB) absorbs UV-A radiation with a peak at 354 nm. . Unique Ingredient Identifier. Improve clinical decision support with information on. Simply click "Create a New List" and enter a name. Filters certain UV rays to protect the skin or hair from the harmful effects of these rays. In vitro phototoxicity was assessed using 3T3 fibroblast cultures. Would you like email updates of new search results? Puglia C, Damiani E, Offerta A, Rizza L, Tirendi GG, Tarico MS, Curreri S, Bonina F, Perrotta RE. Economic, social, environmental, technological, and political factors have been taken into consideration while assessing the growth of the particular region/country. It also has good solubility, excellent formula flexibility, and good compatibility with other UV filters and cosmetic ingredients. Need more context for understanding these highlights? 2012;7(12):e46187. Grbovi et al. Patent review on photostability enhancement of avobenzone and its formulations. or Bulk Inquiry * Please select Quantity before adding items. All Tags have been converted to separate Lists, and your bookmarked items have been saved to a "Bookmarks" List. Based on the findings of a rat study assessing dermal or percutaneous absorption, only a minor amount of diethylamino hydroxybenzoyl hexyl benzoate will undergo percutaneous absorption and most of the compounds will remain in the upper layers of the stratum corneum . UL and the UL logo are trademarks of UL LLC 2023 All Rights Reserved. Diethylamino hydroxybenzoyl hexyl benzoate is an organic compound used in sunscreens to absorb UVA radiation. 3. We extended the investigation to Ethylhexyl Triazone (EHT) and Diethylhexyl Butamido Triazone (DBT), two 1,3,5-Triazine filters that became standardly used UVB filters in systems with BMDBM and without OCR. Download EWG's Healthy Living App. In rat and porcine skin, the percutaneous absorption was 0.10 0.12 g/cm^2 or 0.04 0.05% . The aim of the present study was to investigate the photochemical behavior of DHHB and its photostabilizing effect on avobenzone (AVO) in different sunscreen formulations. Everything you need to know about the cosmetic ingredient DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE, CAS number 302776-68-7, families (UV chemical filter, Regulated), functions (Stabilising, Uv absorber, Uv filter). This ingredient is present in 1. . Consult a medical specialist if you experience any disorder or side effects such as redness, swelling or itchiness. Keep out of reach of children ii. Diethylamino Hydroxybenzoyl Hexyl Benzoate, Octyl Triazone (ethylhexyl Triazone). Diethylamino Hydroxybenzoyl Hexyl Benzoate gilt als empfehlenswert. These results suggest why DHHB did not work as a photostabilizer on AVO singlet excited state. 2017 Mar 1;99:299-309. doi: 10.1016/j.ejps.2016.12.031. : 302776-68-7 Get it tomorrow November 29 by noon. It includes: DUROSOFT PG10-O: which is a natural O/W emulsifier and emollient. Diethylamino hydroxybenzoyl hexyl benzoate (INCI) is an organic compound used in Archived from the original (PDF) on 2008-08-14. MFCI Co.,Ltd. The mechanism of interaction between DHHB and AVO was investigated by steady state and time-resolved fluorescence spectroscopy. Ang ilan sa mga epekto ay maaaring maging bihirang ngunit possibleng maging malubha. Epub 2014 Dec 19. InChI=1S/C24H31NO4/c1-4-7-8-11-16-29-24(28)20-13-10-9-12-19(20)23(27)21-15-14-18(17-22(21)26)25(5-2)6-3/h9-10,12-15,17,26H,4-8,11,16H2,1-3H3, hexyl 2-[4-(diethylamino)-2-hydroxybenzoyl]benzoate, CCCCCCOC(=O)C1=CC=CC=C1C(=O)C1=CC=C(C=C1O)N(CC)CC. Pharmacists also advise patients not to drink . language of work or name. Proprietary Name: Calming Days Vegan Sunscreen. Accessibility 2- (4- (Diethylamino)-2-hydroxybenzoyl)benzoic acid | C18H19NO4 - PubChem compound Summary 2- (4- (Diethylamino)-2-hydroxybenzoyl)benzoic acid Cite Download Contents 1 Structures 2 Names and Identifiers 3 Chemical and Physical Properties 4 Spectral Information 5 Related Records 6 Chemical Vendors 7 Use and Manufacturing 8 Safety and Hazards Diethylamino hydroxybenzoyl hexyl benzoate is a photostable UV-A absorber. Diethylamino hydroxybenzoyl hexyl benzoate (DHHB) as additive to the UV filter avobenzone in cosmetic sunscreen formulations Evaluation of the photochemical behavior and photostabilizing effect Camila Martins Kawakami, Leandro N. C. Mximo, +2 authors L. R. Gaspar Published 1 March 2017 Chemistry European Journal of Pharmaceutical Sciences When you define a new List, the current item is automatically added to it. Minimizing the overexposure of human skin to ultraviolet radiation that may lead to acute and chronic photodamage, diethylamino hydroxybenzoyl hexyl benzoate is an oil-soluble UV filter that may be incorporated in the oil phase of emulsions . This site needs JavaScript to work properly. SUN PROJECT SKIN-RELIEF SUNCREAM- diethylamino hydroxybenzoyl hexyl benzoate, ethylhexyl triazone, methylene bis-benzotriazolyl tetramethylbutylphenol, diethylhexyl butamido triazone cream If this SPL contains inactivated NDCs listed by the FDA initiated compliance action, they will be specified as such. Diethylamino Hydroxybenzoyl Hexyl Benzoate CAS # 302776-68-7 SYNONYM Benzoic Acid, 2- [4- (Diethylamino)-2-Hydroxybenzoyl]-, Hexyl Ester Typical Product Specifications NOTES Used as a shield against UVA radiation and skin damage. The formulations were subjected to photostability studies by HPLC and spectrophotometry. The absence of an interaction does not necessarily mean no interactions exist. Epub 2015 Aug 15. However, UL assumes no responsibility or liability for the accuracy of the information contained on this website and strongly encourages that upon final product or material selection information is validated with the manufacturer. Diethylamino Hydroxybenzoyl Hexyl Benzoate provides excellent free radicals protection and is ideal for long-lasting sun care and anti-aging face care products. 1 Ingredient Found for "DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE" DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE. Nachfolgend finden Sie eine Liste der mglichen Nebenwirkungen, die in der Medizin, die Alkohol/Diethylamino Hydroxybenzoyl Hexylbenzoat / Alcohol / Diethylamino Hydroxybenzoyl Hexyl Benzoate enthalten, auftreten knnen. Instead of one collection of bookmarked items, create as many collections, called "Lists," as you need. 302776-68-7. Molecular Formula CHNO. CAS no. . The uses of diethylamino hydroxybenzoyl hexyl benzoate are diverse - so search around and find precisely what you need. Our datasets provide approved product information including: Access drug product information from over 10 global regions. DHHB has excellent photostability and compatibility with other UV absorbers and other cosmetic ingredients. 2017 Mar 1;99:299-309. doi: 10.1016/j.ejps.2016.12.031. Toxic effects on livestock and pets; Additional toxicological data . Bookshelf 8600 Rockville Pike Eur J Pharm Sci. Innovation is ongoing and as a result, we continually check the latest data on our ingredients. 2010 Apr;9(4):464-9. doi: 10.1039/b9pp00174c. Its molecular structure is that of a benzoyl benzoate ester functionalized with a hydroxyl group and di-ethylamine. English. : 302776-68-7 (English) AICS Chemical ID (BEING DELETED) 42117. In a rat acute oral toxicity study, median LD50 value was reported to be >2000 mg/kg 4. The following lists represent a selection of UL's ChemADVISOR Regulatory Database, curated for Prospector in Compliance Highlights. 302776-68-7. Drug created at December 03, 2015 16:51 / Updated at January 07, 2021 03:13. FOIA DHHB has an absorption maximum of 354 nm. This information should not be interpreted without the help of a healthcare provider. This report analyzes the Diethylamino Hydroxybenzoyl Hexyl Benzoate production by region/country, and the sales (consumption) by region/country. makes their documentation available in the regions indicated below: Diethylamino Hydroxybenzoyl Hexyl Benzoate is very photostable and provides strong UVA protection. DHHB has excellent photostability and compatibility with other UV absorbers and other cosmetic ingredients. Properties Articles 2 Spectrum Names Biological Activity Chemical & Physical Properties MSDS MSDS (Chinese) Safety Information Customs Articles 2 More Articles Synonyms Chemsrc provides CAS#:302776-68-7 MSDS, density, melting point, boiling point, structure, etc. Diethylamino hydroxybenzoyl hexyl benzoate has an absorption maximum of 354 nm. Diethylamino hydroxybenzoyl hexyl benzoate is a photostable UV-A absorber. Diethylamino hydroxybenzoyl hexyl benzoate (DHHB) as additive to the UV filter avobenzone in cosmetic sunscreen formulations - Evaluation of the photochemical behavior and photostabilizing effect Eur J Pharm Sci. Epub 2012 Dec 20. Are you a distributor who is interested in being listed here? Diethylamino Hydroxybenzoyl Hexyl Benzoate is a new generation, chemical sunscreen agent (not available in the US due to impossible FDA regulations) that's designed for high UVA protection and high photostability. It has a chemical structure similar to the classical benxophoenone drug class, and displays good photostability 1. It is used in concentrations up to 10% in sunscreen products, either alone or in combination with other UV absorbers . Diethylamino hydroxybenzoyl hexyl benzoate absorbs in the UV-A range with the peak at 354 nm 1. Evaluation of nanostructured lipid carriers (NLC) and nanoemulsions as carriers for UV-filters: characterization, in vitro penetration and photostability studies. Data Availability: Limited. Two azobenzene derivatives CAB/ACB as reusable sunscreen: UV absorptive capacity and biosafety evaluation. 1426392. Contact us! 53 - May cause long-term adverse effects in the aquatic environment: Safety Description: 61 - Avoid release to the environment.

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