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B8791

Sigma-Aldrich

5-Bromo-5-nitro-1,3-dioxane

≥99%

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About This Item

Empirical Formula (Hill Notation):
C4H6BrNO4
CAS Number:
30007-47-7
Molecular Weight:
212.00
EC Number:
250-001-7
MDL number:
MFCD00101855
UNSPSC Code:
12352119
PubChem Substance ID:
24892094
NACRES:
NA.21

Assay

≥99%

form

powder or crystals

antibiotic activity spectrum

Gram-negative bacteria
Gram-positive bacteria
fungi

application(s)

diagnostic assay manufacturing

Mode of action

enzyme | inhibits

SMILES string

[O-][N+](=O)C1(Br)COCOC1

InChI

1S/C4H6BrNO4/c5-4(6(7)8)1-9-3-10-2-4/h1-3H2

InChI key

XVBRCOKDZVQYAY-UHFFFAOYSA-N

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Application

  • Development of a solid-phase microextraction gas chromatography with microelectron-capture detection method for the determination of 5-bromo-5-nitro-1,3-dioxane in rinse-off cosmetics.: This article details the development of a sensitive analytical method for detecting 5-bromo-5-nitro-1,3-dioxane in cosmetics, enhancing our ability to monitor and ensure the safety of cosmetic products (Fernandez-Alvarez et al., 2010).

Disclaimer

The product is not intended for use as a biocide under global biocide regulations, including but not limited to US EPA′s Federal Insecticide Fungicide and Rodenticide Act, European Biocidal Products Regulation, Canada’s Pest Management Regulatory Agency, Turkey’s Biocidal Products Regulation, Korea’s Consumer Chemical Products and Biocide Safety Management Act (K-BPR) and others.

Signal Word

Danger

Hazard Statements

H302,H314,H410

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Corr. 1A

Storage Class Code

8B - Non-combustible corrosive hazardous materials

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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M Ghannoum et al.
Folia microbiologica, 31(1), 19-31 (1986-01-01)
The mode of action of the antimicrobial agent, 5-bromo-5-nitro-1,3-dioxane (bronidox), was studied in detail for gram-positive and gram-negative bacteria, yeast and fungi. The studies included MIC testing, thiol inhibition of activity, intracellular leakage, oxygen consumption, incorporation of 3H-uridine, scanning electron

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