RUTIN TRIHYDRATE

PRODUCT IDENTIFICATION
CAS NO. 153-18-4 (Base)
250249-75-3  (Trihydrate)

RUTIN 

EINECS NO. 205-814-1
FORMULA C27H30O16· 3H2O
MOL WT. 664.59

H.S. CODE

  

TOXICITY

 
SYNONYMS Rutoside Violaquercitrin
Quercetin-3-rutinoside Vitamin P Quercetin- 3 6-O-(6- deoxy- alpha-L-mannopyranosyl)- beta-D-Glucopyranoside
3-[[6-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl] oxy]-2- (3,4-dihydroxyphenyl)- 5,7-dihydroxy-4H-1-Benzopyran-4-one 3,3',4',5,7-Pentahydroxy flavone-3-rutinoside Sophorin Tanrutin Rutosidum Globulariacitrin 3-Rutinosyl quercetin 115888-40-9 1416-01-9 146525-66-8 158560-09-9 164535-43-7 18449-50-8 48197-72-4 56764-99-9
SMILES

 

CLASSIFICATION

 NATURAL COLORANT / FLAVONES / VITAMINS /

PHYSICAL AND CHEMICAL PROPERTIES

PHYSICAL STATE yellow to greenish crystalline powder or needle
MELTING POINT 195 C
BOILING POINT Decomposes
SPECIFIC GRAVITY  
SOLUBILITY IN WATER Soluble
pH  
VAPOR DENSITY  

AUTOIGNITION

 

NFPA RATINGS

  

REFRACTIVE INDEX

  
FLASH POINT  
STABILITY

Stable under ordinary conditions. Hygroscopic, light sensitive.

GENERAL DESCRIPTION & APPLICATIONS
Rutin, the glycoside form of quercetin, is a bioflavonol having aromatic trimeric heterocyclic structure. It is a naturally occurring pigment. It, chemically 3-[[6-O-(6-deoxy-alpha-L- mannopyranosyl )-beta-D-glucopyranosyl] oxy]-2- (3,4-dihydroxyphenyl) -5,7-dihydroxy-4H-1-Benzopyran-4-one, is a yellow to greenish crystalline powder melting at 190 C. Rutin is classified as vitamin P which increases the strength of the walls of the blood capillaries and regulates their permeability. Others classified as vitamin P are catechin, citrin, eriodictin, hesperetin, hesperidin, nobiletin, quercetin,  sinensetin, and tangeretin. It is not a dietary essential but is known to have the effect on capillary disorders. It may also have an contribution to the total antioxidant activity and detoxifiers. It is also know to have pharmacological action as an anti-inflammatory ,antihistaminic and antiviral agent.

Members of rutin molecules

Product

CAS RN
Rutinose 90-74-4
Rutin 153-18-4
Hesperidin 520-26-3
Narcissin 604-80-8
Tetra(hydroxyethyl)rutoside 6980-20-7
Troxerutin 7085-55-4
Ascorutin 8067-12-7
Rutin sodium sulfate 12768-44-4
Eriocitrin 13463-28-0
Narirutin 14259-46-2
Tamarixetin 7-rutinoside 14265-53-3
Delphinidin-3-rutinoside 15674-58-5
Kaempferol 7-neohesperidoside 17353-03-6
Keracyanin 18719-76-1
Monoxerutin 23869-24-1
Veronicastroside 25694-72-8
Ethoxazorutoside 30851-76-4
Isorhamnetin-3-O-rutinoside-7-O-glucoside 55481-91-9
Rutin S 64755-26-6
Diethanolamine-rutin 69344-84-9
Rutin-N-mustard 85625-48-5
Nirurin 96253-68-8
Rutin sulfate 108916-86-5
Isorhamnetin-3-O-rutinoside-4'-O-glucoside 111393-97-6
Violdelphin 126417-59-2
Swertiamacroside 128585-97-7
D-Glucose-rutin 130603-71-3
Rutin butyryl ester 131981-32-3
2',5,5',7-Tetrahydroxy-flavanone-7-O-rutinoside 153286-43-2
Rutin hydrate 207671-50-9

Rutin trihydrate

250249-75-3
SALES SPECIFICATION

APPEARANCE

 yellow to greenish crystalline powder

ASSAY

 95.0 - 101.5.0 % (anhydrous basis)
IDENTIFICATION

Pass
CHLOROPHYLL

0.004% max
RED PIGMENTS

0.004% max
ASH

0.004% max
LOSS ON DRYING

5.5 - 9.5%
QUERCETIN

5.0% max

IRON

10ppm max

HEAVY METALS

10ppm max
TRANSPORTATION
PACKING 20kgs in fiber drum
HAZARD CLASS not regulated
UN NO.  
OTHER INFORMATION
Hazard Symbols: XI, Risk Phrases: 36/37/38, Safety Phrases: 24/25/28A/37/45

GENERAL DESCRIPTION OF FLAVONOID
Flavonoid is any member of a class of widely distributed biological natural products containing aromatic heterocyclic skeleton of flavan (2-Phenylbenzopyran) but no nitrogen in plants. Generally, flavonoids are biological pigments providing colours from red to blue in flowers, fruit and leaves. Besides their coloring in plants, flavonoids have important roles in the growth and development of plants protection against UV-B radiation forming antifungal barriers antimicrobial, insecticidal and oestrogenic activities plant reproduction. Flavonoids also exhibit a wide range of biological properties including anti-microbial, insecticidal and oestrogenic activities. Flavonoids are usually classified into main 6 subgroups as below plus flavans, neoflavonoids, flavonols, aurons, catechins according to the structural patterns.
  • Flavonols (Hydroxy derivatives of flavone): Fisetin, Galangin, Kaempferide, Kaempferol, Morin, Myricetin, Myricitrin, Quercetin, Quercetrin, Rhamnetin, Robinin, Rutin, Spirenoside
  • Flavones (skeleton: 2-phenylchromen-4-one): Apigenin, Baicalein, Chrysin, Diosmetin, Diosmin, Flavone, Luteolin, Rpoifolin,Tangeretin, Techtochrysin, Rhamnazin, Nobiletin, Natsudaidain.
  • Isoflavones (skeleton: 3-phenylchromen-4-one): Daidzin, Genistein, Irilone, Luteone, Prunetin, Pratensein,
  • Flavonones (derivation by reduction of the 2(3) C=C bond): Eriodictyol, Hesperidin, Hesperetin, Likvirtin, Naringin Naringenin Pinocembrin
  • Flavanols (derivation by reduction of the keto group):(+)-Catechin, (+)-Gallocatechin, (-)-Epicatechin (EC), (-)-Epigallocatechin (EGC), (-)-Epicatechin 3-gallate (ECG), (-)-Epigallocatechin 3-gallate (EGCG), Theaflavin, Theaflavin 3-gallate, Theaflavin 3'-gallate, Theaflavin 3,3' digallate, Thearubigins
  • Anthocyanidins (aglycones of the glycoside anthocyanins): Apigeninidin, Cyanidin, Delphinidin, Diosmetinidin, Guibourtinidin, Fisetinidin, Luteolinidin, Malvidin, Pelargonidin, Peonidin, Robinetinidin, Tricetinidin, Capensinidin, Petunidin, Europinidin, Aurentinidin, Columnidin, 5-Desoxy-malvidin, 5-Desoxy-peonidin, Hirsutinidin, Rosinidin

PRICE INFORMATION