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15448-03-0

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15448-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15448-03-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,4 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 15448-03:
(7*1)+(6*5)+(5*4)+(4*4)+(3*8)+(2*0)+(1*3)=100
100 % 10 = 0
So 15448-03-0 is a valid CAS Registry Number.
InChI:InChI=1/C30H50O5/c1-25(2)14-18-17-8-9-20-27(5)12-11-21(32)26(3,4)19(27)10-13-28(20,6)29(17,7)23(34)24(35)30(18,16-31)22(33)15-25/h8,18-24,31-35H,9-16H2,1-7H3/t18-,19?,20-,21+,22+,23+,24-,27+,28-,29+,30-/m1/s1

15448-03-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S,6aR,6bS,7R,8S,8aS,9S,12aR,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-3,7,8,9-tetrol

1.2 Other means of identification

Product number -
Other names Olean-12-ene-3beta,15alpha,16alpha,22alpha,28-pentol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:15448-03-0 SDS

15448-03-0Upstream product

15448-03-0Downstream Products

15448-03-0Relevant articles and documents

TRITERPENOID SAPONINS FROM LEAVES OF PITTOSPORUM UNDULATUM

Higuchi, Ryuichi,Fujioka, Toshihiro,Iwamoto, Masayo,Komori, Tetsuya,Kawasaki, Toshio,Lassak, Erich V.

, p. 2565 - 2570 (1983)

Two triterpenoid saponins obtained from the leaves of Pittosporum undulatum were characterized on the basis of chemical and spectral evidence as a mixture of 22-O-(2-methylbutyloyl)- and 22-O-(3,3-dimethylacryloyl)-A1-barrigenol 3-O-β-D-glucopyranosyl-(1 -> 2)- 3)>-β-D-glucopyranosiduronic acid and 3-O-β-D-glucopyranosyl-(1 -> 2)- 3)- 4)>>-β-D-glucopyranosiduronic acid.The sugar moieties are the novel oligosaccharides found in A1-barrigenol glycosides.Key Word Index - Pittosporum undulatum; Pittosporaceae; triterpenoid saponin; deacylsaponin; A1-barrigenol 3-O-glycosides.

Medicinal flowers. XXXIII.1 anti-hyperlipidemic and anti-hyperglycemic effects of chakasaponins I-III and structure of chakasaponin IV from flower buds of Chinese tea plant (Camellia sinensis)

Matsuda, Hisashi,Hamao, Makoto,Nakamura, Seikou,Kon'i, Haruka,Murata, Megumi,Yoshikawa, Masayuki

, p. 674 - 680 (2012)

Effects of principal saponins, chakasaponins I-III, from the flower buds of Camellia sinensis cultivated in Fujian province, China on plasma triglyceride (TG) and glucose levels in olive oil or sucrose-loaded mice were examined. Chakasaponins I-III at 50 and 100 mg/kg significantly inhibited increases in plasma TG and glucose levels. Furthermore, they prevented gastric emptying, suggesting that the former inhibitory effect is partly dependent on the inhibition of gastric emptying. In addition, the chemical structure of a new acylated oleanane-type triterpene oligoglycoside, chakasaponin IV, was elucidated on the basis of chemical and physicochemical evidence.

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