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A406

Sigma-Aldrich

1-Acenaphthenol

99%

Synonym(s):

1-Hydroxyacenaphthene

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About This Item

Empirical Formula (Hill Notation):
C12H10O
CAS Number:
6306-07-6
Molecular Weight:
170.21
Beilstein/REAXYS Number:
2048222
EC Number:
228-618-8
MDL number:
MFCD00003808
UNSPSC Code:
12352100
PubChem Substance ID:
24890743
NACRES:
NA.22

assay

99%

mp

145-148 °C (lit.)

SMILES string

OC1Cc2cccc3cccc1c23

InChI

1S/C12H10O/c13-11-7-9-5-1-3-8-4-2-6-10(11)12(8)9/h1-6,11,13H,7H2

InChI key

MXUCIEHYJYRTLT-UHFFFAOYSA-N

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Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Jessica R Murray et al.
Chemical research in toxicology, 32(12), 2538-2551 (2019-11-21)
3-Nitrobenzanthrone (3-NBA) is a suspected human carcinogen present in diesel exhaust. It requires metabolic activation via nitroreduction in order to form DNA adducts and promote mutagenesis. We have determined that human aldo-keto reductases (AKR1C1-1C3) and NAD(P)H:quinone oxidoreductase 1 (NQO1) contribute
Somnath Mallick
Chemosphere, 219, 748-755 (2018-12-18)
A gram-negative bacterium designated as RTSB was isolated from a petroleum-contaminated soil competent of utilizing acenaphthene as the solitary source of carbon and energy. The strain RTSB was identified as a Sphingobacterium species based on the morphological, nutritional and biochemical

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