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Dehydroacetic acid is a synthetic compound characterized by its broad antimicrobial properties, primarily utilized as a preservative in a range of industries including cosmetics, pharmaceuticals, and food products. It functions by disrupting the cellular processes of microorganisms, thereby inhibiting their growth and preventing spoilage or contamination. Recognized for its safety in regulated concentrations and approved for use globally, it remains a valuable asset in maintaining product integrity and safety, although sensitivities in some individuals warrant cautious application.

16807-48-0

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16807-48-0 Usage

Uses

Used in Cosmetics Industry:
Dehydroacetic acid is used as a preservative for cosmetics to maintain product freshness and safety by inhibiting the growth of bacteria and fungi, ensuring a longer shelf life and preventing potential infections or irritations caused by microbial contamination.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, dehydroacetic acid serves as a preservative in various formulations, protecting them from microbial spoilage and ensuring the efficacy, safety, and quality of the medications.
Used in Food Industry:
Dehydroacetic acid is used as a preservative in the food industry to prevent spoilage and extend the shelf life of food products by inhibiting the growth of harmful microorganisms, thus maintaining food safety and quality.

Check Digit Verification of cas no

The CAS Registry Mumber 16807-48-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,8,0 and 7 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 16807-48:
(7*1)+(6*6)+(5*8)+(4*0)+(3*7)+(2*4)+(1*8)=120
120 % 10 = 0
So 16807-48-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H8O4/c1-4-3-6(10)7(5(2)9)8(11)12-4/h3,7H,1-2H3

16807-48-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-acetyl-6-methylpyran-2,4-dione

1.2 Other means of identification

Product number -
Other names 3-Acetyl-6-methyl-2H-pyran-2,4(3H)-dione

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:16807-48-0 SDS

16807-48-0Upstream product

16807-48-0Related news

Ruthenium (II) complexes containing DEHYDROACETIC ACID (cas 16807-48-0) and its imine derivative ligands. Synthesis, characterization and cancer cell growth anti-proliferation activity (GI50) study07/21/2019

Two dehydroacetic acid (DHA, L1H) related imine ligands, L2H and L3H were obtained in moderate yields by reacting DHA with 2,4,6-trimethylaniline and phenylhydrazine, respectively. Refluxing [Ru (η6-p-cymene)Cl2]2 with two equivalents of L1Na, L2H and L3H in methanol generated ruthenium compoun...detailed

16807-48-0Relevant academic research and scientific papers

2,7-Dimethyl-4H-pyrano-2H-pyran-4,5-dione, a Novel Product in the Base-catalysed Self-condensation of Ethyl Acetoacetate : Carbon-13 NMR Spectral Studies

Talapatra, Sunil K.,Basak, Amit,Maiti, Bhim C.,Talapatra, Bani

, p. 546 - 548 (2007/10/02)

Self-condensation of ethyl acetoacetate (EAA) in the presence of a small amount of sodium bicarbonate affords, in addition to the earlier reported dehydroacetic acid (II) (45 percent), a new fused γ-pyrono-pyrone derivative in 40 percent yield, the structure of which has been shown to be 2,7-dimethyl-4H-pyrano-2H-pyran-4,5-dione (III) mainly based on PMR and 13C NMR spectral results and supported by UV, IR and mass spectral data.Compound (II) upon refluxing with EAA in water containing pyridine gives III while EAA under similar condition neither affords II nor III and remains mostly unchanged, supporting the postulated mechanism of formation of III via II. 13C NMR spectral data of II have also been discussed.

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