1 3 Dihydroxyacetone | Substance Information
Di: Samuel
Dihydroxyaceton (abgekürzt DHA, Glyceron) ist ein einfach gebautes Kohlenhydrat mit der Summenformel C 3 H 6 O 3.Preis und Verfügbarkeit anzeigen. Use this link for bookmarking this species for future reference.1,3-Dihydroxyacetone (DHA), the main active ingredient in sunless tanning skin-care preparations and an important precursor for the synthesis of various fine chemicals, is produced on an industrial scale by microbial fermentation of glycerol (HY-B1659) in Gluconobacter oxydans. Molecular Weight: 90. IUPAC Standard InChI: InChI=1S/C3H6O3/c4-1-3 (6)2-5/h4-5H,1-2H2. Slightly soluble in water. DHA sa používa hlavne ako prísada v samoopaľovacej kozmetike.
SAFETY DATA SHEET
: A14189 CAS No .
Dihydroxyacetone, 1,3-Dihydroxidimethyl ketone, DHA, 1,3-Dihydroxidimethyl ketone. Das Molekül kommt in Form des Dihydroxyaceton-3-Phosphates als Zwischenprodukt der Glykolyse vor. Less<< Dihydroxyaceton: SDB (Sicherheitsdatenblätter), Analysenzertifikate und Qualitätszertifikate, Dossiers, Broschüren und andere verfügbare Dokumente. Based on various applications, the global 1,3dihydroxyacetone market was led by cosmetics. Application of WALTZ-16 (1) H decoupling for elimination of large (13) C-(1) H couplings was first tested in thermally polarized glycerol phantoms and .1,3-Dihydroxyacetone (DHA) has been extensively used in the cosmetic and chemical industries [1, 2]. Molecular weight: 90. IUPAC Standard InChIKey: RXKJFZQQPQGTFL-UHFFFAOYSA-N. First-aid measures Eye Contact Rinse immediately with plenty of water, also under the eyelids, for at least 15 minutes. Currently DHA is not regulated under the Cosmetic Regulation (EC) No. In Form von Dihydroxyacetonphosphat ( vgl. Molecular Formula CHO. No 202-494-5) is a cosmetic ingredient with the reported functions of skin conditioning, reducing and tanning.
In one embodiment, DHA is produced in a batch process in less than 20 hours. Get medical attention. Description SDS Pricing; 910139: ≥98 atom % D, ≥95% (CP) Expand.1,3-Dihydroxyacetone dimer is used as a catalytic agent and petrochemical additive. It is an important raw material in the cosmetic industry due to its skin pigmentation property. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product .
Mouse wheel zoom is available as well – the size of the 1,3-dihydroxyacetone molecule can be increased or decreased by scrolling the mouse wheel.1,3-Dihydroxyacetone dimer; EC Number: 202-494-5; Synonyms: 1,3-Dihydroxy-2-propanone dimer; find Sigma-Aldrich-D7753 MSDS, related peer-reviewed papers, technical documents, similar products & more at Sigma-Aldrich Availability We apologize but fulfillment and delivery of this product is delayed. CAS Number: 96-26-4., the selective catalytic oxidation of the secondary –OH bond in glycerol, remains a considerable challenge.Dihydroxyacetone (DHA) is a ketotriose monosaccharide commonly used as the active ingredient in sunless tanning agents (fake tan). All Photos (1) Dihydroxyacetone phosphate lithium salt. A sunless tanning product containing dihydroxyacetone (DHA)Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Dihydroxyaceton CAS 96-26-4
The 1,3-dihydroxyacetone (DHA) (CH 2 OH) 2 C O is the simplest member of the family of ketoses.1,3-Dihydroxyacetone, a sugar alcohol with three carbon atoms, holds widespread applications within the cosmetic, food, and pharmaceutical industries. Skin Contact Wash off immediately with soap and plenty of water while removing all contaminated clothes and shoes. 物理的状態(20℃).Englisch: dihydroxyacetone.DHA can be produced from glycerol by Gluconobacter oxydans [3, 4], which is one of the most frequently used microorganisms in industrial biotechnology for the production of valuable chemicals [5–7].Acidic condition was used to dissociate the dl-glyceraldehyde dimer (2) and 1,3-dihydroxyacetone dimer (3) to their . Soluble in ethanol, ethyl ether, acetone.分子式・分子量. Synonyms: Dihydroxyacetone, 1,3-Dihydroxy-2-propanone, 1,3-Dihydroxyacetone, DHA, Glycerone, NSC 24343. Empirical Formula (Hill Notation): C 6 D 8 H 4 O 6. CAS Registry Number: 96-26-4.1,3-Dihydroxyacetone dimer is primarily used as an ingredient in sunless tanning products. Any bacterial metabolite produced during a metabolic reaction in Escherichia coli .1,3-Dihydroxyacetone dimer SAFETY DATA SHEET Page 1 / 8 Revision Date 18-Feb-2021 Version 2 ALFAAA14189 SECTION 1. Da Dihydroxyaceton kein Stereozentrum aufweist, gilt es eigentlich nicht als Monosaccharid.
Dihydroxyacetone
Composition(s) generated upon use Other types of composition(s) Information on Registered Substances comes from registration dossiers which have been assigned a .Dihydroxyacetone. aus dem durch den . Further, it serves as a reagent in three-carbon nucleophilic or electrophilic component in various reactions. It is about 25 times more effective than the well-known coreactant sodium oxalate. In this study, a series of mesoporous CuO–SnO2 composite oxides were prepared by a hard-template method and used to support Au catalysts for the selective oxidation of glycerol to 1,3 .Dihydroxyaceton. In addition, DHA is also reported to be used in spray cabins in aqueous solutions in concentrations between 8 and 14% with the purpose of obtaining tanned skin without exposure to sunlight or UV radiation. 1,3-Dihydroxypropan-2-on SMILES: C(C(=O)CO)O . Dihydroxyaceton United States Pharmacopeia (USP) Reference Standard; CAS Number: 96-26-4; Synonyms: 1,3-Dihydroxy-2-propanon,1,3-Dihydroxyaceton,DHA,Glyceron,NSC 24343; find USP-1204102 MSDS, related peer-reviewed papers, technical documents, similar products & more at Sigma-Aldrich.1,3-Dihydroxyacetone, a common cosmetic material and food additive, has been successfully explored as an efficient electrochemiluminescence coreactant of Ru(bpy)32+ for the first time. Es ist jedoch wesentlich am Kohlenhydratstoffwechsel beteiligt.If the substance is covered by more than one CLH entry (e.
Substance Information
1,3-Dihydroxyacetone-1,1,3,3-d 4 dimer.A chiral primary alkyl amine, (1S,2S)-2-amino-1-(4-nitrophenyl)propane-1,3-diol (1), was selected as a model compound in this study. Dihydroxyacetone (DHA) is used as a self-tanning agent in leave-on cosmetic products up to 10%.
1,3-dihydroxyacetone (dimer), 62147-49-3
OPINION ON Dihydroxyacetone
Category: flavoring agents: Recommendation for 1,3-dihydroxyacetone (dimer) usage levels up to: not for fragrance use. Contact Technical Service.Major (13) C-(1) H coupling JCH = ∼150 Hz) is introduced after adenosine triphosphate-dependent enzymatic transformation of HP [2-(13) C]dihydroxyacetone to [2-(13) C]glycerol-3-phosphate in vivo.1,3-Dihydroxyacetone: Spec-Chem Industry: Tanbest TM DHA(Dihydroxyactone DHA) Safety Information: Hazards identification Classification of the substance or mixture: GHS Classification in accordance with 29 CFR 1910 (OSHA HCS) None found. Dihydroxyacet o n s, 1,3-Dihydroxypropan-2-on, einfachste Ketose ( Triosen ). ChemSusChem 8 , 853–860 (2015). It is also used as a building block in organic synthesis.In one embodiment, a method comprising reacting glycerol with acetaldehyde or 1,1-diethoxyethane to produce 1,3-dihydroxyacetone (DHA), without using fermentation or direct oxidation of the glycerol is provided. Dihydroxyaceton ( DHA ), také známý jako glyceron, je monosacharid ( trióza) patřící mezi ketózy.Bewertungen: 22
1,3-Dihydroxyacetone dimer 97%
Monoisotopic mass 180. IDENTIFICATION OF THE SUBSTANCE/MIXTURE AND OF THE COMPANY/UNDERTAKING 产品说明:1,3-二羟基丙酮二聚体 Product Description: 1,3-Dihydroxyacetone dimer Cat No.1,3-dihydroxyacetone EC Number: 202-494-5 EC Name: 1,3-dihydroxyacetone CAS Number: 96-26-4 Molecular formula: C3H6O3 IUPAC Name: 1,3-dihydroxyacetone. Summenformel und Strukturformel der chemischen Verbindung Dihydroxyaceton: C 3 H 6 O 3.Additionally, it is used as a cosmetic . Copy Sheet of paper on top of another sheet.The 1,3-dihydroxyacetone molecule shown in the visualization screen can be rotated interactively by keep clicking and moving the mouse button.
1,3-Dihydroxyacetone
For security reasons, the DHA is obtained in an aqueous solution by a biotechnology process. This entity has been manually annotated by the ChEBI Team. jednotky SI a STP (25 °C, 100 kPa). Products are for research use only.6% during 2020-2026 owing to increasing demands for 1, 3-Dihydroxyacetone in the chemical industry.1,3-Dihydroxyacetone (DHA), the main active ingredient in sunless tanning skin-care preparations and an important precursor for the synthesis of various fine chemicals, is produced on an industrial scale by microbial fermentation of glycerol over Gluconobacter oxydans[1]. Molecular Weight 90. Chemical structure: This .
) ist Dihydroxyaceton Zwischenprodukt beim Abbau von Glucose ( Glykolyse, alkoholische Gärung ), aber auch beim Aufbau der Glucose im Rahmen der Gluconeogenese bzw. dl-Glyceraldehyde and 1,3-dihydroxyacetone were in dimeric forms as purchased. The high electrochemiluminescence efficiency allows .1,3-Dihydroxyacetone is a chemical compound that has been used as a reactant in the synthesis of glycerol. M r = 90,078 g/mol.1,3-Dihydroxyacetone (DHA), the main active ingredient in sunless tanning skin-care preparations and an important precursor for the synthesis of various fine chemicals, is produced on an industrial scale by microbial fermentation of glycerol over Gluconobacter oxydans. Obvykle se získává z rostlinných . DHA ist der wesentliche Inhaltsstoff von Selbstbräuner und reagiert mit . Molecular Weight: 188.View the Full Spectrum for FREE! The full spectrum can only be viewed using a FREE account. The simplest member of the class of ketoses and the parent of the class of glycerones. Empirical Formula (Hill Notation): C 3 H 6 O 3. Not for human use. Daten und Eigenschaften .: The Expert Panel also publishes separate extensive . Některá data mohou pocházet z datové položky. disodium tetraborate EC no. Compare Product No. 1,3-Dihydroxyacetone dimer 97%; CAS Number: 26776-70-5; Synonyms: 2,5-Dihydroxydioxane-2,5-dimethanol; find Sigma-Aldrich-W403326 MSDS, . This Thermo Scientific brand product was originally part of the Alfa Aesar product portfolio.
1,3-Dihydroxyacetone Dimer
96-26-4, EC Number 202-494-5. Its significance lies in being a vital intermediate compound for synthesizing various substances, including glycerol, the primary constituent of soap, and glycerol ethers. Use levels for FEMA GRAS flavoring substances on which the FEMA Expert Panel based its judgments that the substances are generally recognized as safe (GRAS). Synonym(s): 1-Hydroxy-3-(phosphonooxy)-2-propanone lithium salt, DHAP, .1,3-Dihydroxyacetone (DHA) is a commercially important chemical and widely used in cosmetics, pharmaceuticals, and food industries as it prevents excessive water evaporation, and provides anti-ultraviolet radiation protection and antioxidant activity. You can also browse global suppliers,vendor,prices,Price,manufacturers of 1,3 . [1] Často pochádza z rastlinných zdrojov, ako sú cukrová repa a cukrová trstina, alebo fermentácie glycerolu . Reaxys Registry Number. Dihydroxyaceton ist ein Monosaccharid mit drei Kohlenstoffatomen ( Triose) und einer Ketogruppe am C 2 -Atom ( Ketose ); es weist folgende Formel auf: H 2 COH-CO-H 2 COH. In one embodiment, the DHA is produced in a continuous .Other names: 2-Propanone, 1,3-dihydroxy-; Chromelin; Dihyxal; Otan; Oxantin; Oxatone; Soleal; Triulose; Viticolor; 1,3-Dihydroxy-2-propanone; 1,3-Dihydroxyacetone; NSC-24343; 1,3-Dihydroxypropanone; 1,3-Dihydroxydimethyl ketone; Ketochromin Permanent link for this species. We are working to minimize these . The reaction mechanism for the formation of 1,3-dihydroxyacetone involves the reaction of metal hydroxides with glycerol to form an intermediate product, which then . Dihydroxyacetone (DHA) with the chemical name 1,3-Dihydroxy-2-propanone (CAS No.Englische Bezeichnung Dihydroxyacetone 1,3-Dihydroxyacetone; Glycerone 1,3-Dihydroxypropan-2-one . Inhalation Remove . Chemische Formeln. A ketotriose consisting of acetone bearing hydroxy substituents at positions 1 and 3.Dihydroxyacetón alebo DHA [1] či glycerón [1] je triózový sacharid . 1,3-Dihydroxyacetone is also used for synthesis of new .More>> Dihydroxyacetone for synthesis.CHEBI:16016 – dihydroxyacetone. Currently, the industrial production of DHA is based on a biotechnological synthetic route .The 1, 3-Dihydroxyacetone market is predicted to witness a significant growth of nearly 4. SDB; Analysenzertifikat; Synonyme: DHA, 1,3-Dihydroxy-2-propanon CAS-Nr. After the production, a crystallization process is . GHS Label elements, including precautionary statements Pictogram Hazard statement(s) None .Material Safety Data Sheet or SDS for Dihydroxyacetone 110845 from Merck for download or viewing in the browser. It is a waterproof skin dye used to darken light or unpigmented areas of skin affected by vitiligo, scars or other causes.Visit ChemicalBook To find more 1,3-Dihydroxyacetone(96-26-4) information like chemical properties,Structure,melting point,boiling point,density,molecular formula,molecular weight, physical properties,toxicity information,customs codes. Catalog Number 110845 Product Name DihydroxyacetoneFormula: C 3 H 6 O 3.1,3-Dihydroxyacetone Revision Date 14-Feb-2020 4. EC Index Number: 202-494-5.
215–540–4, is covered by three harmonisations: 005–011–00–4; 005–011–01–1 and 005–011–02–9), CLH information cannot be displayed in the InfoCard as the difference between the CLH classifications requires manual interpretation or verification. It accounted for more than 40% share of the market in 2019. ChemSpider ID 3391434.1,3-Dihydroxyacetone Dimer. DHA is synonymous with glycerone or 1,3-dihydroxypropan-2-one. Dihydroxyacetone (DHA, 1,3-dihydroxy-2-propanone, C 3 H 6 O 3) is a widely known ketotriose used as raw material to produce chemical substances of industrial importance, such as 1,2-propylene glycol, 1,3-propanediol, lactic acid, methotrexate, surfactants, etc (Khanna et al. Mechanistic studies on the cascade conversion of 1,3-dihydroxyacetone and formaldehyde into α-hydroxy-γ-butyrolactone. The biosynthesis of DHA in . Average mass 180.Bewertungen: 89
Dihydroxyacetone MSDS
Používá se hlavně jako součást přípravků na opálení bez ultrafialového záření.
dihydroxyacetone (CHEBI:16016)
It is the simplest ketone formed from glycerol and a hydroxyl group. PubChem Substance ID.Selective catalytic oxidation of polyols, e.
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