1,3-Dihydroxyaceton Chemische Eigenschaften,Einsatz,Produktion Methoden

S-S?tze Betriebsanweisung:

S24/25:Berührung mit den Augen und der Haut vermeiden.

Chemische Eigenschaften

white powder

Occurrence

A derivative of naturally occurring starch

Verwenden

1,3-Dihydroxyacetone can be used as artificial tanning agent.

Definition

ChEBI: Dihydroxyacetone is a ketotriose consisting of acetone bearing hydroxy substituents at positions 1 and 3. The simplest member of the class of ketoses and the parent of the class of glycerones. It has a role as a metabolite, an antifungal agent, a human metabolite, a Saccharomyces cerevisiae metabolite, an Escherichia coli metabolite and a mouse metabolite. It is a ketotriose and a primary alpha-hydroxy ketone.

synthetische

1,3-dihydroxyacetone (DHA) is prepared by acetalization, oxidation, and hydrolysis of glycerol. Usually produced commercially from Bacillus macerans or Bacillus circulans fermentation of starch or starch hydrolysate

Allgemeine Beschreibung

Dihydroxyacetone (DHA) is a browning ingredient widely used in cosmetics such as sunless tanning formulations. It participates in a chemical staining reaction called Milliard reaction in which it reacts with the amino groups of proteins to result in a mixture of high molecular weight pigments.
Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards.

Sicherheitsprofil

Mutation data reported. When heated to decompositionit emits acrid smoke and irritating vapors.

Sicherheit(Safety)

Cells that were treated with 1,3-Dihydroxyacetone (DHA) showed dose- and time-dependent changes that included cytoplasmic budding, chromatin condensation, and cell detachment. There was a significant decrease in cell proliferation after 24 hours of DHA exposure. After exposure to a 5% DHA solution for 21 days, epidermal thickening and dermatitis of the skin were noted in laboratory animals. After 42 days of treatment with the same solution, hyperplastic and dyskeratotic changes and moderate inflammatory reactions were seen. Long-lasting topical tanning products contain the sugars DHA or erythrulose, which cause a "Maillard reaction" when contacting proteins in the outer layers of the stratum corneum and epidermis. This reaction happens when free amino acids from skin proteins combine with DHA in the stratum corneum. This combination creates the tanned appearance of skin. Results are generally seen within a few hours of application. UV light exposure is not needed to initiate this chemical reaction[1].

1,3-Dihydroxyaceton Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte

1,3-Dihydroxyaceton Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Firmenname	Telefon	E-Mail	Land	Produktkatalog	Edge Rate
Hebei Zhuanglai Chemical Trading Co.,Ltd	+8613343047651	admin@zlchemi.com	China	3002	58
CD Chemical Group Limited	+8615986615575	info@codchem.com	China	20342	58
Hebei Weibang Biotechnology Co., Ltd	+8617732866630	bess@weibangbio.com	China	18148	58
Hebei Kingfiner Technology Development Co.Ltd	+86-15532196582 +86-15373005021	lisa@kingfinertech.com	China	3009	58
Shanghai Likang New Materials Co., Limited	+86-16631818819 +86-17736933208	3684455296@qq.com	China	9300	58
Hebei Weibang Biotechnology Co., Ltd	+8615350571055	Sibel@weibangbio.com	China	6087	58
ZhenYiBio Technology Inc	+8615309206328	alexxue@zhenyibio.com	China	296	58
Hebei Weibang Biotechnology Co., Ltd	+8615531157085	abby@weibangbio.com	China	8806	58
Hebei Yanxi Chemical Co., Ltd.	+8617531153977	allison@yan-xi.com	China	5857	58
Hebei Chuanghai Biotechnology Co,.LTD	+86-13131129325	sales1@chuanghaibio.com	China	5889	58

96-26-4(1,3-Dihydroxyaceton)Verwandte Suche:

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• Chromelin
• NSC-24343
• Oxantin
• Oxatone
• Protosol
• Soleal
• Triulose
• Viticolor
• 1,3-DIHYDROXYACETONE
• 1,3-DIHYDROXY-2-PROPANE
• 1,2-DIHYDROXY-2-PROPANONE
• DIHYDROXYACETONE CRYSTALLINE
• 1,3-Dihydroxyaceton
• 1,3-DIHYDROXYACETONE (DHA)
• Dihydroxyacetone ,98%
• Dihydroxyacetone (250 mg)
• 1,1-Dihydroxy-propan-2-one
• 1,3-Dihydroxyacetone, 98%+
• 1,3-Dihydroxyacetone Monomer
• DIHYDROXYACETONE FOR SYNTHESIS
• Nizatidine Impurity 3
• Bis(hydroxymethyl)ketone
• dihydroxyacetone (monomer)
• 1,3-DIHYDROXYACETONE (DHA) Cas RN 96-26-4
• 1,3-Dihydroxyacetone D4
• PROPANE-1,3-DIOL-2-ONE
• 1,3-dihydroxy-2-propanon
• 1,3-Dihydroxydimethyl ketone
• 1,3-Dihydroxypropanone
• Aliphatic ketone
• Dihyxal
• Ketochromin
• Otan
• DIHYDROXYACETONE
• 1,3-DIHYDROXYACTONE
• 1,3-DIHYDROXY-2-PROPANONE
• 2-Propanone, 1,3-dihydroxy-
• 1,3-dihydroxypropan-2-one
• Glycerone
• 3-Dihydroxyacetone
• 1,3 Dihydroxypropan-2-One(Dihydroxyacetone)
• 4-Butylresorcino
• DHA (Dihydroxyacetone)
• Dihydroxyacetone, DHA
• Hexane 110-54-3
• Glycerol Impurity 15
• 1,3-DihydroxyacetonChemicalbooke
• 1,3-Dihydroxyacetone in Water
• Dihydroxyacetone/1,3-Dihydroxyacetone
• 96-26-4
• Pharmaceutical intermediates
• Imidazoles
• 96-26-4
• bc0001