1,2-DISTEAROYL-RAC-GLYCERO-3-PHOSPHOCHOLINE

Base Information

Chemical Name:1,2-DISTEAROYL-RAC-GLYCERO-3-PHOSPHOCHOLINE
CAS No.:816-93-3
Molecular Formula:C₄₄H₈₈NO₈P
Molecular Weight:790.158
Hs Code.:
Mol file:816-93-3.mol

Synonyms:1,2-DISTEAROYL-RAC-GLYCERO-3-PHOSPHOCHOLINE;DL-ALPHA-PHOSPHATIDYLCHOLINE, DISTEAROYL;DL-BETA,GAMMA-DISTEAROYL-ALPHA-LECITHIN;dl-A-phosphatidylcholine;DL-A-PHOSPHATIDYLCHOLINE, DISTEAROYL;dl-α-phosphatidylcholine, distearoyl;DL-b,g-Distearoyl-a-lecithin

Suppliers and Price of 1,2-DISTEAROYL-RAC-GLYCERO-3-PHOSPHOCHOLINE

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

AK Scientific
1,2-Distearoyl-rac-glycero-3-phosphocholine
250mg
$ 217.00

AK Scientific
1,2-Distearoyl-rac-glycero-3-phosphocholine
1g
$ 392.00

American Custom Chemicals Corporation
DL-ALPHA-PHOSPHATIDYLCHOLINE, DISTEAROYL 95.00%
100MG
$ 737.35

American Custom Chemicals Corporation
DL-ALPHA-PHOSPHATIDYLCHOLINE, DISTEAROYL 95.00%
500MG
$ 1312.20

Sigma-Aldrich
DL-α-Phosphatidylcholine, distearoyl ≥98%
100mg
$ 235.00

Total 5 raw suppliers

Chemical Property of 1,2-DISTEAROYL-RAC-GLYCERO-3-PHOSPHOCHOLINE

Chemical Property:

PSA：121.00000
LogP:13.24240
Storage Temp.:-15°C

Purity/Quality:

98%Min ^*data from raw suppliers

1,2-Distearoyl-rac-glycero-3-phosphocholine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 1,2-DISTEAROYL-RAC-GLYCERO-3-PHOSPHOCHOLINE

There total 18 articles about 1,2-DISTEAROYL-RAC-GLYCERO-3-PHOSPHOCHOLINE 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: 67.0%

: 57-11-4
stearic acid

: 816-94-4,4539-70-2,66701-63-1,816-93-3,18603-43-5
{2-[(2,3-bis-stearoyloxy-propoxy)-hydroxy-phosphoryloxy]-ethyl}-trimethyl-ammonium betaine

Guidance literature:: stearic acid; With dicyclohexyl-carbodiimide; In dichloromethane; for 2h; Reflux;

alumina-supported glycerophosphatidylcholine; In dichloromethane; Solvent;

Reference yield: 54.5%

: 51063-97-9
DL-α,β-distearin

: 55357-38-5
choline tosylate

: 816-94-4,4539-70-2,66701-63-1,816-93-3,18603-43-5
{2-[(2,3-bis-stearoyloxy-propoxy)-hydroxy-phosphoryloxy]-ethyl}-trimethyl-ammonium betaine

Guidance literature:: DL-α,β-distearin; With triethylamine; trichlorophosphate; In chloroform; at 10 ℃; for 4.5h; Inert atmosphere;

choline tosylate; With pyridine; In chloroform; for 15.5h; Inert atmosphere;

Reference yield:

: 111-63-7,9003-95-6
vinyl stearate

: 34688-34-1,563-24-6
glycerolcholine phosphate

: 816-94-4,4539-70-2,66701-63-1,816-93-3,18603-43-5
{2-[(2,3-bis-stearoyloxy-propoxy)-hydroxy-phosphoryloxy]-ethyl}-trimethyl-ammonium betaine

: 17364-19-1,5655-17-4
1-stearoyl-sn-glycero-3-phosphocholine

: 57-11-4
stearic acid

Guidance literature:: Lecitase surfactant-coated (modified)-immobilized enzyme complex on Duolite A₅₆₈; In tert-butyl alcohol; at 60 - 70 ℃; for 96.5 - 200h; Enzyme kinetics; Enzymatic reaction;