Xanthoxylin

Modify Date: 2024-01-04 21:54:00

Xanthoxylin Structure
Xanthoxylin structure
Common Name Xanthoxylin
CAS Number 90-24-4 Molecular Weight 196.200
Density 1.2±0.1 g/cm3 Boiling Point 355.1±37.0 °C at 760 mmHg
Molecular Formula C10H12O4 Melting Point 80-84 °C(lit.)
MSDS Chinese USA Flash Point 141.2±20.0 °C

 Use of Xanthoxylin


Xanthoxylin (Xanthoxyline) is isolated from Zanthoxylum simulans. Xanthoxylin (Xanthoxyline) has antifungal and antispasmodic activities[1][2].

 Names

Name 4',6'-Dimethoxy-2'-hydroxyacetophenone
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.2±0.1 g/cm3
Boiling Point 355.1±37.0 °C at 760 mmHg
Melting Point 80-84 °C(lit.)
Molecular Formula C10H12O4
Molecular Weight 196.200
Flash Point 141.2±20.0 °C
Exact Mass 196.073563
PSA 55.76000
LogP 2.37
Vapour Pressure 0.0±0.8 mmHg at 25°C
Index of Refraction 1.528

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Risk Phrases R36/37/38
Safety Phrases S26-S36/37/39
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2914509090

 Synthetic Route

 Customs

HS Code 2914509090
Summary HS:2914509090 other ketones with other oxygen function VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%

 Articles11

More Articles
Collateral sensitivity of resistant MRP1-overexpressing cells to flavonoids and derivatives through GSH efflux.

Biochem. Pharmacol. 90(3) , 235-45, (2014)

The multidrug resistance protein 1 (MRP1) is involved in multidrug resistance of cancer cells by mediating drug efflux out of cells, often in co-transport with glutathione (GSH). GSH efflux mediated b...

Antinociceptive action of 2-(4-bromobenzoyl)-3-methyl-4,6-dimethoxy benzofuran, a novel xanthoxyline derivative on chemical and thermal models of nociception in mice.

J. Pharmacol. Exp. Ther. 278(1) , 304-12, (1996)

The antinociceptive effect of the novel xanthoxyline derivative 2-(4-bromobenzoyl)-3-methyl-4-6-dimethoxy benzofuran) (BMDB), given i.p., p.o., s.c., subplantarly, intrathecally or by i.c.v. routes wa...

Synthesis of chalcone analogues with increased antileishmanial activity.

Bioorg. Med. Chem. 14(5) , 1538-45, (2006)

Eighteen analogues of an active natural chalcone were synthesized using xanthoxyline and some derivatives, and these analogues were tested for selective activity against both promastigotes and intrace...

 Synonyms

2-HYDROXY-4,6-DIMETHOXYACETOPHENONE
MFCD00017243
Brevifolin (VAN)
EINECS 201-978-3
4,6-Dimethoxy-2-hydroxyacetophenone
Phloracetophenone 4,6-Dimethyl Ether
2,4-Dimethoxy-6-hydroxyacetophenone
Acetophenone, 2'-hydroxy-4',6'-dimethoxy-
Ethanone, 1-(2-hydroxy-4,6-dimethoxyphenyl)-
1-(2-Hydroxy-4,6-dimethoxyphenyl)ethanone
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