Lipid IVA

Base Information

Chemical Name:Lipid IVA
CAS No.:91841-27-9
Molecular Formula:C₆₈H₁₃₀N₂O₂₃P₂
Molecular Weight:1405.73
Hs Code.:
DSSTox Substance ID:DTXSID301344466
Nikkaji Number:J609.054K
Wikidata:Q27104050
Metabolomics Workbench ID:51941
Mol file:91841-27-9.mol

Synonyms:compound 406;lipid A precursor IA;lipid A precursor, Salmonella typhimurium;lipid A precursors, bacterial;lipid A precursors, Pseudomonas;lipid A precursors, Salmonella;lipid IVA;tetraacyl disaccharide 1,4'-bisphosphate

Suppliers and Price of Lipid IVA

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

Biosynth Carbosynth
Lipid IVa
0.5 mg
$ 1625.00

Biosynth Carbosynth
Lipid IVa
0.2 mg
$ 740.00

Biosynth Carbosynth
Lipid IVa
0.1 mg
$ 395.00

Total 2 raw suppliers

Chemical Property of Lipid IVA

Chemical Property:

PSA：413.01000
LogP:11.65580
XLogP3:14.4
Hydrogen Bond Donor Count:12
Hydrogen Bond Acceptor Count:23
Rotatable Bond Count:62
Exact Mass:1404.85396239
Heavy Atom Count:95
Complexity:2080

Purity/Quality:

95% ^*data from raw suppliers

Lipid IVa ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCCCCCC(CC(=O)NC1C(C(C(OC1OP(=O)(O)O)COC2C(C(C(C(O2)CO)OP(=O)(O)O)OC(=O)CC(CCCCCCCCCCC)O)NC(=O)CC(CCCCCCCCCCC)O)O)OC(=O)CC(CCCCCCCCCCC)O)O
Isomeric SMILES:CCCCCCCCCCC[C@H](CC(=O)N[C@@H]1[C@H]([C@@H]([C@H](O[C@@H]1OP(=O)(O)O)CO[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)OP(=O)(O)O)OC(=O)C[C@@H](CCCCCCCCCCC)O)NC(=O)C[C@@H](CCCCCCCCCCC)O)O)OC(=O)C[C@@H](CCCCCCCCCCC)O)O

Technology Process of Lipid IVA

There total 3 articles about Lipid IVA 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:

: C₁₂₅H₁₇₈N₂O₂₃P₂

: 91841-27-9
2-deoxy-6-O-(2-deoxy-3-O-((R)-3-hydroxytetradecanoyl)-2-((R)-3-hydroxytetradecanoylamino)-β-D-glucopyranosyl)-3-O-((R)-3-hydroxytetradecanoyl)-2-((R)-3-hydroxytetradecanoylamino)-α-D-glucopyranose 1,4'-bisphosphate

Guidance literature:: With hydrogen; palladium; In tetrahydrofuran; at 20 ℃; for 4h; under 5250.42 Torr;
DOI:10.1246/bcsj.70.1435

Reference yield:

: C₈₀H₁₃₈N₂O₂₃P₂

: 91841-27-9
2-deoxy-6-O-(2-deoxy-3-O-((R)-3-hydroxytetradecanoyl)-2-((R)-3-hydroxytetradecanoylamino)-β-D-glucopyranosyl)-3-O-((R)-3-hydroxytetradecanoyl)-2-((R)-3-hydroxytetradecanoylamino)-α-D-glucopyranose 1,4'-bisphosphate

Guidance literature:: With hydrogen; platinum(IV) oxide; In tetrahydrofuran; hexane; for 2h; under 5148.6 Torr; Ambient temperature;
DOI:10.1246/bcsj.60.2197