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Safety Information

A77903

Sigma-Aldrich

1-Aminopyrene

97%

Synonym(s):

1-Pyrenamine, 3-Aminopyrene

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About This Item

Empirical Formula (Hill Notation):
C16H11N
CAS Number:
1606-67-3
Molecular Weight:
217.27
Beilstein:
1875737
EC Number:
216-521-3
MDL number:
MFCD00004140
UNSPSC Code:
12352100
PubChem Substance ID:
24891279
NACRES:
NA.22

Quality Level

100

Assay

97%

form

powder

mp

115-117 °C (lit.)

SMILES string

Nc1ccc2ccc3cccc4ccc1c2c34

InChI

1S/C16H11N/c17-14-9-7-12-5-4-10-2-1-3-11-6-8-13(14)16(12)15(10)11/h1-9H,17H2

InChI key

YZVWKHVRBDQPMQ-UHFFFAOYSA-N

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Application

  • Synthesis and evaluation of aromatic stationary phases based on linear solvation energy relationship model for expanded application in supercritical fluid chromatography.: Explores the use of 1-Aminopyrene in the development of advanced stationary phases for chromatography, enhancing the efficiency and application range in pharmaceutical and environmental analysis (Ge et al., 2024).
  • Two-Dimensional Porphyrinic Metal-Organic Framework Composites as a Photocatalytic Platform for Chemoselective Hydrogenation.: Highlights the integration of 1-Aminopyrene into metal-organic frameworks, providing a new avenue for creating highly efficient photocatalytic systems for organic synthesis, relevant to both academic research and industrial chemical manufacturing (Dong et al., 2023).
  • Exploiting and Engineering Neuroglobin for Catalyzing Carbene N-H Insertions and the Formation of Quinoxalinones.: Discusses the role of 1-Aminopyrene in enhancing enzymatic reactions within engineered proteins, paving the way for novel synthetic pathways in pharmaceutical research (Sun et al., 2023).

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302

Precautionary Statements

P264 - P270 - P301 + P312 - P501

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

A77903-250MG:
A77903-1G:
A77903-BULK:
A77903-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
SHBR4768
SHBN1287
SHBK8921
SHBH8471
SHBF0663V

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Dina Mukha et al.
ChemSusChem, 13(10), 2684-2692 (2020-02-19)
The construction of bias- and donor-free photobioelectrochemical cells for the generation of light-triggered electrical power is presented. The developed oxygen reduction biocathodes are based on bilirubin oxidase (BOD) that originates from Myrothecium verrucaria (MvBOD) and a thermophilic Bacillus pumilus (BpBOD).
Man Jae Park et al.
Chemical communications (Cambridge, England), 48(89), 11008-11010 (2012-10-06)
Excess electron transfer dynamics in DNA hairpins was investigated by femtosecond laser flash photolysis of a donor-DNA-acceptor system using N,N-dimethylaminopyrene and diphenylacetylene as an electron donor and acceptor, respectively. It was revealed that the excess electron hopping rate between T's
P D Josephy et al.
Mutation research, 429(2), 199-208 (1999-10-20)
The mutagenic actions of many chemicals depend on the activities of bacterial "mutagenesis proteins", which allow replicative bypass of DNA lesions. Genes encoding these proteins occur on bacterial chromosomes and plasmids, often in the form of an operon (such as
Junkuo Gao et al.
Dalton transactions (Cambridge, England : 2003), 41(39), 12185-12191 (2012-08-30)
A novel pyrene covalently-attached polyoxometalate (POM) hybrid has been synthesized and fully characterized. The attractive electronic and photophysical properties of pyrene derivatives make the hybrid promising for studying and understanding electron transfer mechanisms in organic-functionalized POMs. The hybrid has an
Susan Huyck et al.
Journal of exposure science & environmental epidemiology, 20(7), 650-655 (2010-05-06)
Biomonitoring of exposures to toxins is an important tool for monitoring public health and safety. Using this tool, exposures are typically measured by the collection of biological specimens such as blood and urine samples. Urine sampling represents a more convenient
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