Tormentic acid

Base Information

Chemical Name:Tormentic acid
CAS No.:13850-16-3
Molecular Formula:C₃₀H₄₈O₅
Molecular Weight:488.708
Hs Code.:2918199890
NSC Number:720893
UNII:9WL8LH7U78
DSSTox Substance ID:DTXSID40930135
Nikkaji Number:J126.654C
Wikipedia:Tormentic_acid
Wikidata:Q15634134
Metabolomics Workbench ID:128769
ChEMBL ID:CHEMBL239077
Mol file:13850-16-3.mol

Synonyms:tormentic acid

Suppliers and Price of Tormentic acid

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Usbiological
Tormentic acid
5mg
$ 439.00

TRC
TormenticAcid
1mg
$ 105.00

Crysdot
Tormenticacid 95+%
5mg
$ 461.00

AvaChem
Tormentic acid
100mg
$ 1890.00

AvaChem
Tormentic acid
20mg
$ 890.00

AvaChem
Tormentic acid
5mg
$ 390.00

AvaChem
Tormentic acid
1mg
$ 190.00

Arctom
Tormenticacid
5mg
$ 158.00

American Custom Chemicals Corporation
TORMENTIC ACID 95.00%
5MG
$ 505.01

Ambeed
(1R,2R,4aS,6aS,6bR,8aR,10R,11R,12aR,12bR,14bS)-1,10,11-Trihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4a-carboxylicacid 95+%
250mg
$ 261.00

Total 84 raw suppliers

Chemical Property of Tormentic acid

Chemical Property:

Vapor Pressure:4.86E-17mmHg at 25°C
Melting Point:273 °C
Refractive Index:1.579
Boiling Point:602.7 °C at 760 mmHg
PKA:4.47±0.70(Predicted)
Flash Point:332.3 °C
PSA：97.99000
Density:1.19g/cm³
LogP:5.17520
Storage Temp.:Sealed in dry,Room Temperature
Solubility.:Pyridine (Sparingly)
XLogP3:5
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:1
Exact Mass:488.35017463
Heavy Atom Count:35
Complexity:956

Purity/Quality:

99% ^*data from raw suppliers

Tormentic acid ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O
Isomeric SMILES:C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(C[C@H]([C@@H](C5(C)C)O)O)C)C)[C@@H]2[C@]1(C)O)C)C(=O)O
Uses Tormentic Acid is isolated from Tormentil rhizomes and has inhibitory effect on carcinognenesis. In addition, Tormentic Acid has been implicated to be a potential therapeutic candidate for the prevention of APAP-induced liver injury by inhibiting oxidative stress and inflammation.

Technology Process of Tormentic acid

There total 11 articles about Tormentic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 68.2%

: 1309589-79-4
2α,19α-dihydroxy-5α,9α-urs-12-en-3-one-28-oic acid-28-O-β-D-glucopyranosyl ester

: 53155-25-2,119725-19-8,13850-16-3
tormentic acid

: 95298-47-8,146356-82-3,88515-58-6
rosamultin

Guidance literature:: With sodium tetrahydroborate; In methanol; at 0 ℃; for 1h;
DOI:10.1016/j.phytochem.2014.03.002

Reference yield:

: 3-O-p-coumaroyltormentic acid

: 53155-25-2,119725-19-8,13850-16-3
tormentic acid

Guidance literature:: 3-O-p-coumaroyltormentic acid; With water; sodium hydroxide; at 20 ℃; for 15h;

With sulfuric acid; In water;
DOI:10.1016/j.bmc.2010.01.010