Hesperidin

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Names

[ CAS No. ]:
520-26-3

[ Name ]:
Hesperidin

[Synonym ]:
usafcf-3
Hesperetin 7-rhamnoglucoside,Hesperitin-7-rutinoside
VITAMIN P
Hespeidin
Hespiridin
Hesperiden
Neobiletin
cirantin
MFCD00075663
Hesperetin7-rutinoside
Cirontin
Hesperidoside
Hesperetin7-rhamnoglucoside
Hesperidin
EINECS 208-288-1

Chemical & Physical Properties

[ Density]:
1.7±0.1 g/cm3

[ Boiling Point ]:
930.1±65.0 °C at 760 mmHg

[ Melting Point ]:
250-255 °C (dec.)(lit.)

[ Molecular Formula ]:
C28H34O15

[ Molecular Weight ]:
610.561

[ Flash Point ]:
305.5±27.8 °C

[ Exact Mass ]:
610.189758

[ PSA ]:
234.29000

[ LogP ]:
1.78

[ Vapour Pressure ]:
0.0±0.3 mmHg at 25°C

[ Index of Refraction ]:
1.695

MSDS

Click to get detail MSDS

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
MK6650000
CHEMICAL NAME :
Hesperidin
CAS REGISTRY NUMBER :
520-26-3
BEILSTEIN REFERENCE NO. :
0075140
LAST UPDATED :
199701
DATA ITEMS CITED :
3
MOLECULAR FORMULA :
C28-H34-O15
MOLECULAR WEIGHT :
610.62
WISWESSER LINE NOTATION :
T66 BO EVT&J CR CQ DO1& GQ IO- BT6OTJ CQ DQ EQ F1O- BT6OTJ CQ DQ EQ F1 GLUCO RHAMNO

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
1 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
NTIS** National Technical Information Service. (Springfield, VA 22161) Formerly U.S. Clearinghouse for Scientific & Technical Information. Volume(issue)/page/year: AD277-689 *** NIOSH STANDARDS DEVELOPMENT AND SURVEILLANCE DATA *** NIOSH OCCUPATIONAL EXPOSURE SURVEY DATA : NOHS - National Occupational Hazard Survey (1974) NOHS Hazard Code - 84694 No. of Facilities: 156 (estimated) No. of Industries: 2 No. of Occupations: 10 No. of Employees: 8654 (estimated)

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R22

[ Safety Phrases ]:
S22-S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ RTECS ]:
MK6650000

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • alpha-Glucosyl Hesperidin
  • Ethanol
  • 3,2',6'-trihydroxy-4-methoxy-4'-(O6-α-L-rhamnopyranosyl-β-D-glucopyranosyloxy)-trans-chalcone
  • hesperetin 7-O-rutinoside

DownStream

  • Isoferulic acid
  • Diosmin
  • Hesperetin
  • 4-methylumbelliferyl-rutinoside
  • 6-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucose
  • Ethyl rutinoside

Articles

Bio-refinery of orange peels waste: a new concept based on integrated green and solvent free extraction processes using ultrasound and microwave techniques to obtain essential oil, polyphenols and pectin.

Ultrason. Sonochem. 24 , 72-9, (2015)

In this study, extraction of essential oil, polyphenols and pectin from orange peel has been optimized using microwave and ultrasound technology without adding any solvent but only "in situ" water whi...

Effects of pectinase clarification treatment on phenolic compounds of pummelo (Citrus grandis l. Osbeck) fruit juice.

J. Food Sci. Technol. 52 , 5057-65, (2015)

The purpose of this study is to investigate the changes occured on phenolic compounds between two Malaysian varieties of pummelo fruit juice: Ledang (PO55) and Tambun (PO52) post-enzymatic clarificati...

Curcumin and hesperidin improve cognition by suppressing mitochondrial dysfunction and apoptosis induced by D-galactose in rat brain.

Food Chem. Toxicol. 74 , 51-9, (2014)

D-galactose, a reducing sugar, induces oxidative stress resulting in alteration in mitochondrial dynamics and apoptosis of neurons. Curcumin and hesperidin are antioxidants possessing multimodal funct...


More Articles

Related Compounds

  • hesperidin
  • G-hesperidin
  • Methyl hesperidin
  • a-D-Glucosyl hesperidin
  • Hesperidin methylchalcone
  • Hesperidin dihydrochalcone
  • 4-[2-(ethoxymethyl)morpholin-4-yl]-3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4-oxobutanoic acid
  • 2-[(2R)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-methylbutanamido]benzoic acid
  • 2-{1-[(2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)butanamido]ethyl}-1,3-thiazole-4-carboxylic acid
  • 2-{[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-methylpentanamido]methyl}-3-methylbutanoic acid
  • 2-{4-[3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanoyl]-1,1-dioxo-1lambda6-thiomorpholin-3-yl}acetic acid
  • 2-{1-[3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)cyclohexyl]-N-(prop-2-yn-1-yl)formamido}acetic acid
  • 2-{1-[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4-methoxyphenyl]-N-methylformamido}acetic acid
  • 5-[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2-methylpentanamido]hexanoic acid
  • 3-cyclopropyl-3-{[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)cyclopentyl]formamido}propanoic acid
  • (2R)-2-[5-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4-methylpentanamido]-3,3-dimethylbutanoic acid
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