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Merck
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Documenti

65800

Sigma-Aldrich

2-Methylanthraquinone

technical, ≥95% (HPLC)

Sinonimo/i:

2-MAQ

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About This Item

Formula empirica (notazione di Hill):
C15H10O2
Numero CAS:
84-54-8
Peso molecolare:
222.24
Beilstein:
2050523
Numero CE:
201-539-6
Numero MDL:
MFCD00001235
Codice UNSPSC:
12352100
ID PubChem:
24884160
NACRES:
NA.22

Grado

technical

Saggio

≥95% (HPLC)

Impurezze

3-4% 1-methylanthraquinone

P. eboll.

236-238 °C/10 mmHg (lit.)

Punto di fusione

170-173 °C (lit.)

Stringa SMILE

Cc1ccc2C(=O)c3ccccc3C(=O)c2c1

InChI

1S/C15H10O2/c1-9-6-7-12-13(8-9)15(17)11-5-3-2-4-10(11)14(12)16/h2-8H,1H3
NJWGQARXZDRHCD-UHFFFAOYSA-N

Informazioni sul gene

human ... CTSG(1511) , ELA2(1991)

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Applicazioni

2-Methylanthraquinone may be used in the preparation of potential bioreducible anthraquinone derivatives.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

408.2 °F - closed cup

Punto d’infiammabilità (°C)

209 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Gloves

Certificati d'analisi (COA)

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Sigma-Aldrich

244511

Toluene

Giampaolo Gori et al.
The Annals of occupational hygiene, 53(1), 27-32 (2008-11-04)
A new gas chromatographic/mass spectrometric (GC/MS) method was developed to detect 2-methylanthraquinone (2-MeA) in wood dust. 2-MeA is present in teak wood (a suspected human carcinogen) but not in oak, beech, mahogany, birch, ash or pine. The method involved collection
D Biswas et al.
Bioresource technology, 102(2), 1284-1288 (2010-09-11)
Projected decline in future wood resources has prompted researchers to try various additives in existing pulping processes for fiber yield improvement. Many studies have been conducted in the past aimed at improving kraft pulp yield with the use of additives
Emily L Whitson et al.
Journal of natural products, 75(3), 394-399 (2012-02-09)
Barleria alluaudii and Diospyros maritima were both investigated as part of an ongoing search for synergistic TRAIL (tumor necrosis factor-α-related apoptosis-inducing ligand) sensitizers. As a result of this study, two naphthoquinone epoxides, 2,3-epoxy-2,3-dihydrolapachol (1) and 2,3-epoxy-2,3-dihydro-8-hydroxylapachol (2), both not previously
Helen Sheridan et al.
Journal of natural products, 74(1), 82-85 (2010-12-23)
Two new furanonaphthoquinones, (3R)-7-methoxy-α-dunnione (5) and (3R)-6-hydroxy-7-methoxy-α-dunnione (6), along with the known (3R)-dunnione (1), (3R)-α-dunnione (2), (3R)-7-hydroxy-α-dunnione (3), and 1-hydroxy-2-methylanthraquinone (4), were isolated from in vitro cultures of Streptocarpus dunnii. The structures of compounds 5 and 6 were established by
Maria Helena Verdan et al.
Journal of natural products, 73(8), 1434-1437 (2010-08-06)
Three new aromatic epsilon-lactones, aggregatins A (1), B (2), and C (3), a new naphthoquinone derivative, aggregatin D (4), and three known anthraquinones, 2-methylanthraquinone, 7-methoxy-2-methylanthraquinone, and 7-hydroxy-2-methylanthraquinone, were isolated from the tubers of Sinningia aggregata (Gesneriaceae). Compounds 1 and 4
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