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Safety Information

H31204

Sigma-Aldrich

9-Hydroxyfluorene

96%

Synonym(s):

9-Fluorenol

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About This Item

Empirical Formula (Hill Notation):
C13H10O
CAS Number:
1689-64-1
Molecular Weight:
182.22
EC Number:
216-879-0
MDL number:
MFCD00001135
UNSPSC Code:
12352100
PubChem Substance ID:
24895548
NACRES:
NA.22

Quality Level

100

Assay

96%

mp

153-154 °C (lit.)

SMILES string

OC1c2ccccc2-c3ccccc13

InChI

1S/C13H10O/c14-13-11-7-3-1-5-9(11)10-6-2-4-8-12(10)13/h1-8,13-14H

InChI key

AFMVESZOYKHDBJ-UHFFFAOYSA-N

Pictograms

Environment
GHS09

Signal Word

Warning

Hazard Statements

H410

Precautionary Statements

P273 - P391 - P501

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

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

H31204-25G:
H31204-5G:
H31204-1KG:
H31204-VAR:
H31204-BULK:

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Certificates of Analysis (COA)

Lot/Batch Number
STBK8574
STBK8234
STBJ9424
STBJ6754
STBJ4413

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L Bastiaens et al.
Research in microbiology, 152(10), 849-859 (2002-01-05)
The promoter probe mini-Tn5-luxAB-tet was used to create a luxAB transcriptional fusion responding to fluorene in the fluorene utilising bacterium Sphingomonas sp. LB126. The mutant strain, named L-132, was impaired in fluorene utilisation and strongly emitted light upon addition of
Derek Dunn et al.
Bioorganic & medicinal chemistry letters, 22(11), 3751-3753 (2012-05-02)
In searching for a next generation molecule to the novel wake promoting agent modafinil (compound 1), a series of fluorene-derived wakefulness enhancing agents were developed and evaluated in rat. Extensive pharmacokinetic studies of a potent member of the series (compound
C Chen et al.
Drug metabolism and disposition: the biological fate of chemicals, 12(4), 421-426 (1984-07-01)
Fluoren-9-ol and fluoren-9-one were used as model substrates to study microsomal metabolism of alcohols and carbonyl compounds. It was found that there was an oxidoreductase(s) present in the microsomal preparation that catalyzed interconversion of this alcohol and ketone using pyridine
Microbial reduction of 9-fluorenone to 9-hydroxyfluorene in carbon-filtered water: a confounding factor in an aquatic bioassay of 9-fluorenone with larvae of the midge, Chironomus tentans (Fabr.).
P W O'Keefe et al.
Bulletin of environmental contamination and toxicology, 75(6), 1060-1066 (2006-01-13)
Biban Gill et al.
Analytical and bioanalytical chemistry, 411(7), 1397-1407 (2019-01-27)
Urinary 1-hydroxypyrene (OH-Pyr) is widely used for biomonitoring human exposures to polycyclic aromatic hydrocarbons (PAHs) from air pollution and tobacco smoke. However, there have been few rigorous validation studies reported to ensure reliable OH-Pyr determination for occupational health and risk
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