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Galangin

CAS No.
548-83-4
Chemical Name:
Galangin
Synonyms
Galengin;GALANGIN;Galangin-RM;NORIZALPININ;Galangin 99%;GALANGIN hplc;Galangin (6CI);Galangin, >=98%;Galangin[282200];Galangin Standard
CBNumber:
CB8413460
Molecular Formula:
C15H10O5
Molecular Weight:
270.24
MDL Number:
MFCD00006833
MOL File:
548-83-4.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-04-21 17:10:26
Product description Number Pack Size Price
Galangin phyproof? Reference Substance PHL89505 20MG $350
Galangin analytical standard 92342 25 mg $266
Galangin autophagy inducing flavonoid 282200 25mg $212
Galangin autophagy inducing flavonoid 282200 100mg $634
Galangin min. 98.0 % G0370 25MG $41
More product size

Galangin Properties

Melting point 214-215 °C(lit.)
Boiling point 333.35°C (rough estimate)
Density 1.2319 (rough estimate)
refractive index 1.6000 (estimate)
storage temp. room temp
solubility Acetone (Slightly), Ethyl Acetate (Slightly)
pka 6.32±0.40(Predicted)
form Solid
color Light Yellow to Yellow
Merck 14,4339
BRN 272179
Major Application food and beverages
Cosmetics Ingredients Functions SKIN PROTECTING
InChI InChI=1S/C15H10O5/c16-9-6-10(17)12-11(7-9)20-15(14(19)13(12)18)8-4-2-1-3-5-8/h1-7,16-17,19H
InChIKey VCCRNZQBSJXYJD-UHFFFAOYSA-N
SMILES C1(C2=CC=CC=C2)OC2=CC(O)=CC(O)=C2C(=O)C=1O
LogP 3.322 (est)
CAS DataBase Reference 548-83-4(CAS DataBase Reference)
FDA UNII 142FWE6ECS
UNSPSC Code 41116107
NACRES NA.79

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P301+P312+P330
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-37/39
WGK Germany  3
RTECS  LK9275500
10
HS Code  29329990
Storage Class 11 - Combustible Solids
Hazard Classifications Acute Tox. 4 Oral
NFPA 704
1
2 0

Galangin price More Price(62)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich PHL89505 Galangin phyproof? Reference Substance 548-83-4 20MG $350 2026-03-19 Buy
Sigma-Aldrich 92342 Galangin analytical standard 548-83-4 25 mg $266 2026-03-19 Buy
Sigma-Aldrich 282200 Galangin autophagy inducing flavonoid 548-83-4 25mg $212 2026-03-19 Buy
Sigma-Aldrich 282200 Galangin autophagy inducing flavonoid 548-83-4 100mg $634 2026-03-19 Buy
TCI Chemical G0370 Galangin min. 98.0 % 548-83-4 25MG $41 2026-03-19 Buy
Product number Packaging Price Buy
PHL89505 20MG $350 Buy
92342 25 mg $266 Buy
282200 25mg $212 Buy
282200 100mg $634 Buy
G0370 25MG $41 Buy

Galangin Chemical Properties,Uses,Production

Description

Galangin is a flavonoid naturally found in herbs used in traditional medicine. Like many flavonoids, it has potent antioxidant properties. It also has anti-inflammatory actions related to suppression of signaling through NF-κB in mice. Galangin acts as an antagonist of the aryl hydrocarbon receptor, inducing apoptosis in cancer cells. It also inhibits cytochrome P450 isoform 1A1 with an IC50 value of less than 1 μM.

Chemical Properties

Yellow powder

Uses

CYP1A1 inhibitor, vasodilator

Uses

Galangin is a flavanoid found in Alpinia officinarum, galangal rhizome (Alpinia galanga) and in propolis. Galangin has been show to inhibit proliferation of estrogen receptor-positive MCF-7 human breast cancer cells as well as delay of mammary tumorigenesis.

Definition

ChEBI: A 7-hydroxyflavonol with additional hydroxy groups at positions 3 and 5 respectively.

General Description

Galangin is a flavonoid isolated from members of the Zingiberaceae family, which are mainly used for herbal medicines.

Biochem/physiol Actions

Galangin exhibits antioxidant, anti-apoptotic, anti-inflammatory and anti-obesity properties. In addition, it also possesses anti-genotoxic activity against environmental and dietary carcinogens. Galangin inhibits cancer growth by hindering cancer cell proliferation, induction of apoptosis and autophagy and inhibition of metastasis. Galangin also has an ability to inhibit CYP1A1 (Cytochrome P450, family 1, member A1) activity.

Anticancer Research

Galangin is a flavonol that is derived from Alpinia officinarum, a plant from the gingerfamily, grown in Southeast Asia. The extract from the rhizome suppresses cellproliferation of hepatocellular carcinoma cells (Su et al. 2013). ER stress is inducedby galangin as is evident by rise in concentration of cytosolic Ca2+ and other UPRtarget genes like CHOP, GRP 78 and GRP 94. The ER is a major storage site forintracellular calcium. Normal functioning of ER chaperones is disrupted by calciumexhaustion in ER which produces ER stress and hence activation of UPR (Hotamisligil2010; Mekahli et al. 2011). CHOP and 4-polybutyric acid siRNA, well-known ERstress inhibitor, substantially blocked stress induced by galangin in the HCC cell line.To sum up, ER stress is upregulated by galangin, inhibiting cancer cell proliferation,and galangin can prove to be an effective anticancer agent (Su et al. 2013).

References

[1] GARRY DUTHIE  Philip M. Antioxidant capacity of flavonoids in hepatic microsomes is not reflected by antioxidant effects in vivo.[J]. Oxidative Medicine and Cellular Longevity, 2012, 2012: 165127. DOI: 10.1155/2012/165127
[2] WANG-JIAN ZHA. Galangin Abrogates Ovalbumin-Induced Airway Inflammation via Negative Regulation of NF-κB.[J]. Evidence-based Complementary and Alternative Medicine, 2013, 2013: 767689. DOI: 10.1155/2013/767689
[3] S A QUADRI. The bioflavonoid galangin blocks aryl hydrocarbon receptor activation and polycyclic aromatic hydrocarbon-induced pre-B cell apoptosis.[J]. Molecular Pharmacology, 2000, 58 3: 515-525. DOI: 10.1124/mol.58.3.515
[4] WENJING ZHANG. Galangin induces B16F10 melanoma cell apoptosis via mitochondrial pathway and sustained activation of p38 MAPK.[J]. Cytotechnology, 2013, 65 3: 447-455. DOI: 10.1007/s10616-012-9499-1
[5] ALAINA M FORBES. Synthesis and anticancer activity of new flavonoid analogs and inconsistencies in assays related to proliferation and viability measurements.[J]. International journal of oncology, 2014, 45 2: 831-842. DOI: 10.3892/ijo.2014.2452
[6] H P CIOLINO  G C Y. The flavonoid galangin is an inhibitor of CYP1A1 activity and an agonist/antagonist of the aryl hydrocarbon receptor[J]. British Journal of Cancer, 1999, 79 9-10: 1340-1346. DOI: 10.1038/sj.bjc.6690216

480-66-0
548-83-4
Synthesis of Galangin from 2',4',6'-Trihydroxyacetophenone monohydrate
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View Lastest Price from Galangin manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Galangin pictures 2026-04-21 Galangin
548-83-4
US $30.00-77.00 / mg 99.54% 10g TargetMol Chemicals Inc.
Galangin pictures 2025-06-13 Galangin
548-83-4
US $0.00 / kg 1kg 99.8% 1000 kg BINBO BIOLOGICAL CO.,LTD
Galangin pictures 2024-04-15 Galangin
548-83-4
US $1.00 / mg 100mg 0.99 5ton/month ANHUI SHENGZHIKAI BIOTECHNOLOGY CO.,LTD
  • Galangin pictures
  • Galangin
    548-83-4
  • US $30.00-77.00 / mg
  • 99.54%
  • TargetMol Chemicals Inc.
  • Galangin pictures
  • Galangin
    548-83-4
  • US $0.00 / kg
  • 99.8%
  • BINBO BIOLOGICAL CO.,LTD
  • Galangin pictures
  • Galangin
    548-83-4
  • US $1.00 / mg
  • 0.99
  • ANHUI SHENGZHIKAI BIOTECHNOLOGY CO.,LTD

Galangin Spectrum

4H-1-Benzopyran-4-one,3,5,7-trihydroxy-2-phenyl Galengin 3,5,7-Trihydroxy-2-phenyl-4h-benzopyran-4-one Galangin Standard Galangin, 98%, from Alpinia officinarum 3,5,7-Trihydroxy-2-phenyl-4H-chroMen-4-one Galangin, froM Alpinia officinaruM Galangin, >=98% GALANGIN, AUTOPHAGY INDUCING FLAVONO 3,5,7-trihydroxy-2-phenyl-4h-benzopyran-4-on 3,5,7-trihydroxy-flavon NORIZALPININ GALANGIN 3,5,7-trihydroxy-2-phenyl-chromen-4-one 3,5,7-TRIHYDROXYFLAVONE 3,5,7-Trihydroxyflavone (Galangin) 3,5,7-Trihydroxyflavone,97% GALANGIN hplc GALANGIN WITH HPLC 2-Phenyl-3,5,7-trihydroxy-4H-1-benzopyran-4-one 3,5,7-Trihydroxy-2-phenyl-4H-1-benzopyran-4-one 3,5,7-trihydroxy-2-phenyl-4-benzopyrone 7-Trihydroxyflavone 3,5,7-trihydroxy-2-phenyl-1-benzopyran-4-one Galangin (6CI) Galangin-RM Galangin, 10 mM in DMSO Galangin 99% Galangin[282200] 548-83-4 Antineoplastic Flavanols chemical reagent pharmaceutical intermediate phytochemical reference standards from Chinese medicinal herbs (TCM). standardized herbal extract