ChemicalBook >> CAS DataBase List >>1,3-Dihydroxyacetone

1,3-Dihydroxyacetone

CAS No.
96-26-4
Chemical Name:
1,3-Dihydroxyacetone
Synonyms
DIHYDROXYACETONE;1,3-dihydroxypropan-2-one;Dihyxal;Glycerone;Ketochromin;1,3-Dihydroxypropanone;1,3-DIHYDROXY-2-PROPANONE;2-Propanone, 1,3-dihydroxy-;Otan;Aliphatic ketone
CBNumber:
CB6306814
Molecular Formula:
C3H6O3
Lewis structure
c3h6o3 lewis structure
Molecular Weight:
90.08
MDL Number:
MFCD00004670
MOL File:
96-26-4.mol
Last updated:2024-11-19 15:53:33

1,3-Dihydroxyacetone Properties

Melting point 75-80 °C
Boiling point 107.25°C (rough estimate)
Density 1.1385 (rough estimate)
vapor pressure 0.002-0.33Pa at 20-50℃
FEMA 4033 | DIHYDROXYACETONE
refractive index 1.4540 (estimate)
storage temp. Store at +2°C to +8°C.
solubility >112.4 mg/mL in DMSO; >5.09 mg/mL in EtOH with ultrasonic
pka 12.45±0.10(Predicted)
form powder
color White
Odor at 100.00 %. minty
Odor Type minty
Water Solubility >250 g/L (20 ºC)
JECFA Number 1716
Stability Stable. Combustible. Hygroscopic.
LogP -1.95 at 20℃
Surface tension 68.85mN/m at 1g/L and 20℃
CAS DataBase Reference 96-26-4(CAS DataBase Reference)
FDA 21 CFR 73.1150; 73.2150
Substances Added to Food (formerly EAFUS) DIHYDROXYACETONE (MONOMER)
EWG's Food Scores 1-4
FDA UNII O10DDW6JOO
NIST Chemistry Reference 2-Propanone, 1,3-dihydroxy-(96-26-4)
EPA Substance Registry System 2-Propanone, 1,3-dihydroxy- (96-26-4)
Cosmetics Info Dihydroxyacetone

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H319-H315-H335
Precautionary statements  P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362
Safety Statements  24/25
HS Code  29141900
Toxicity CHROMELIN ? DIHYDROXYACETONE ? 1,3DIHYDROXYACETONE ? 1,3-DIHYDROXYPROPANONE ? DIHYXAL ? NSC-24343 ? OTAN ? OXATONE ? SOLEAL ? 2PROPANONE, 1,3-DIHYDROXY- ? TRIULOSE ? VITICOLOR

1,3-Dihydroxyacetone price More Price(25)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 8.20482 Dihydroxyacetone for synthesis 96-26-4 100G $60.8 2024-03-01 Buy
Sigma-Aldrich 8.20482 Dihydroxyacetone for synthesis 96-26-4 250G $128 2024-03-01 Buy
Frontier Specialty Chemicals JK368677 Dihydroxyacetone 98% 96-26-4 250g $144 2021-12-16 Buy
Matrix Scientific 119322 1,3-Dihydroxyacetone 95+% 96-26-4 500g $178 2021-12-16 Buy
Biosynth Carbosynth FD07750 1,3-Dihydroxyacetone 96-26-4 100g $200 2021-12-16 Buy
Product number Packaging Price Buy
8.20482 100G $60.8 Buy
8.20482 250G $128 Buy
JK368677 250g $144 Buy
119322 500g $178 Buy
FD07750 100g $200 Buy

1,3-Dihydroxyacetone Chemical Properties,Uses,Production

Chemical Properties

Dihydroxyacetone has a characteristic sweet, cooling aroma.

Chemical Properties

white powder

Occurrence

A derivative of naturally occurring starch

Uses

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

Uses

These Secondary Standards are qualified as Certified Reference Materials. These are suitable for use in several analytical applications including but not limited to pharma release testing, pharma method development for qualitative and quantitative analyses, food and beverage quality control testing, and other calibration requirements.

Uses

1,3-Dihydroxyacetone (DHA) is a self-tanning agent used in cosmetics designed to provide a tanned appearance without the need for sun exposure. It is also a uV protector and a color additive. As a self-tanning agent, it reacts with amino acids found on the skin’s epidermal layer. Its effects last only a few days as the color it provides fades with the natural shedding of the stained cells. Reportedly, it works best on slightly acidic skin. DHA, when combined with lawsone, becomes an FDA Category I (approved) uV protectant. In 1973, the FDA declared that DHA is safe and suitable for use in cosmetics or drugs that are applied to color the skin, and has exempted it from color additive certification.

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.

Preparation

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

Taste threshold values

Reported to have a taste threshold value lower than that of sucrose with a detection level of 3.9 to 27 ppm and a recognition level of 11 to 52 ppm.

General Description

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.

Safety Profile

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

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].

References

[1] Gallagher, Mary. “Exposureto Dihydroxyacetone in Sunless Tanning Products.”Journal of the Dermatology Nurses'Association 10(1): 11-17.

56-81-5
96-26-4
Synthesis of 1,3-Dihydroxyacetone from Glycerol
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View Lastest Price from 1,3-Dihydroxyacetone manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
1,3-Dihydroxyacetone pictures 2024-11-24 1,3-Dihydroxyacetone
96-26-4
US $500.00-300.00 / kg 1kg 99% 5000 HEBEI SHENGSUAN CHEMICAL INDUSTRY CO.,LTD
1,3-Dihydroxyacetone pictures 2024-11-22 1,3-Dihydroxyacetone
96-26-4
US $100.00-65.00 / kg 1kg 99% 20ton Hebei Zhuanglai Chemical Trading Co.,Ltd
1,3-Dihydroxyacetone pictures 2024-11-22 1,3-Dihydroxyacetone
96-26-4
US $0.00 / KG 25KG 98%min 30tons/month WUHAN FORTUNA CHEMICAL CO., LTD
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 96-26-4 Pharmaceutical intermediates Imidazoles 96-26-4 bc0001