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H43601

Sigma-Aldrich

2-Hydroxy-4-methylquinoline

97%

Synonym(s):

4-Methyl-2-quinolinol, 4-Methylcarbostyril

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About This Item

Empirical Formula (Hill Notation):
C10H9NO
CAS Number:
607-66-9
Molecular Weight:
159.18
EC Number:
210-139-0
MDL number:
MFCD00006745
UNSPSC Code:
12352100
PubChem Substance ID:
24895639
NACRES:
NA.22

Quality Level

100

Assay

97%

mp

221-223 °C (lit.)

SMILES string

Cc1cc(O)nc2ccccc12

InChI

1S/C10H9NO/c1-7-6-10(12)11-9-5-3-2-4-8(7)9/h2-6H,1H3,(H,11,12)

InChI key

APLVPBUBDFWWAD-UHFFFAOYSA-N

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

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

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Certificates of Analysis (COA)

Lot/Batch Number
STBL4547
STBJ7105
STBJ1212
STBH4990
STBH2954

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Markus Brinkmann et al.
Chemical research in toxicology, 32(4), 698-707 (2019-03-22)
Hydroxylation of polyaromatic compounds through cytochromes P450 (CYPs) is known to result in potentially estrogenic transformation products. Recently, there has been an increasing awareness of the importance of alternative pathways such as aldehyde oxidases (AOX) or N-methyltransferases (NMT) in bioactivation

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