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HEXADECANOIC-7,7,8,8-D4 ACID

Base Information
  • Chemical Name:HEXADECANOIC-7,7,8,8-D4 ACID
  • CAS No.:75736-49-1
  • Molecular Formula:C16H32O2
  • Molecular Weight:260.397
  • Hs Code.:
  • Mol file:75736-49-1.mol
HEXADECANOIC-7,7,8,8-D4 ACID

Synonyms:PALMITIC ACID (7,7,8,8-D4);HEXADECANOIC-7,7,8,8-D4 ACID;Hexadecanoic Acid-7,7,8,8-D4

Suppliers and Price of HEXADECANOIC-7,7,8,8-D4 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
  • Medical Isotopes, Inc.
  • Hexadecanoic Acid-7,7,8,8-d4
  • 0.1 g
  • $ 750.00
  • Medical Isotopes, Inc.
  • Palmitic Acid-7,7,8,8-d4
  • 0.1 g
  • $ 550.00
  • American Custom Chemicals Corporation
  • HEXADECANOIC-7,7,8,8-D4 ACID 95.00%
  • 5MG
  • $ 500.82
Total 7 raw suppliers
Chemical Property of HEXADECANOIC-7,7,8,8-D4 ACID
Chemical Property:
  • PSA:37.30000 
  • LogP:5.55230 
Purity/Quality:

99%, *data from raw suppliers

Hexadecanoic Acid-7,7,8,8-d4 *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses Hexadecanoic-7,7,8,8-d4 Acid (CAS# 75736-49-1) is a useful isotopically labeled research compound.
Technology Process of HEXADECANOIC-7,7,8,8-D4 ACID

There total 13 articles about HEXADECANOIC-7,7,8,8-D4 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:
Guidance literature:
Multi-step reaction with 10 steps
1: 85 percent / NBS; PPh3 / dimethylformamide / 1 h / 0 °C
2: 73 percent / BuLi / tetrahydrofuran; hexane / -78 - 20 °C
3: NBS / acetone; H2O / 0.02 h / -30 °C
4: 97 percent / LiAlH4 / diethyl ether / 20 °C
5: 92 percent / Et3N / CH2Cl2 / 2 h / 20 °C
6: 95 percent / LiAlH4 / diethyl ether / 16 h / 20 °C
7: 97 percent / D2 / RhCl(PPh3)3 / benzene / 36 h
8: 89 percent / aq. HCl / methanol / 24 h / 20 °C
9: IBX / dimethylsulfoxide / 12 h / 20 °C
10: 88 mg / H2SO4; CrO3 / acetone; H2O
With chromium(VI) oxide; hydrogenchloride; N-Bromosuccinimide; lithium aluminium tetrahydride; n-butyllithium; sulfuric acid; triethylamine; triphenylphosphine; deuterium; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione; RhCl(PPh3)3; In tetrahydrofuran; methanol; diethyl ether; hexane; dichloromethane; water; dimethyl sulfoxide; N,N-dimethyl-formamide; acetone; benzene; 10: Jones oxidation;
DOI:10.1021/jo061592s
Guidance literature:
Multi-step reaction with 9 steps
1: 73 percent / BuLi / tetrahydrofuran; hexane / -78 - 20 °C
2: NBS / acetone; H2O / 0.02 h / -30 °C
3: 97 percent / LiAlH4 / diethyl ether / 20 °C
4: 92 percent / Et3N / CH2Cl2 / 2 h / 20 °C
5: 95 percent / LiAlH4 / diethyl ether / 16 h / 20 °C
6: 97 percent / D2 / RhCl(PPh3)3 / benzene / 36 h
7: 89 percent / aq. HCl / methanol / 24 h / 20 °C
8: IBX / dimethylsulfoxide / 12 h / 20 °C
9: 88 mg / H2SO4; CrO3 / acetone; H2O
With chromium(VI) oxide; hydrogenchloride; N-Bromosuccinimide; lithium aluminium tetrahydride; n-butyllithium; sulfuric acid; triethylamine; deuterium; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione; RhCl(PPh3)3; In tetrahydrofuran; methanol; diethyl ether; hexane; dichloromethane; water; dimethyl sulfoxide; acetone; benzene; 9: Jones oxidation;
DOI:10.1021/jo061592s
Guidance literature:
Multi-step reaction with 4 steps
1: 97 percent / D2 / RhCl(PPh3)3 / benzene / 36 h
2: 89 percent / aq. HCl / methanol / 24 h / 20 °C
3: IBX / dimethylsulfoxide / 12 h / 20 °C
4: 88 mg / H2SO4; CrO3 / acetone; H2O
With chromium(VI) oxide; hydrogenchloride; sulfuric acid; deuterium; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione; RhCl(PPh3)3; In methanol; water; dimethyl sulfoxide; acetone; benzene; 4: Jones oxidation;
DOI:10.1021/jo061592s
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