D-galactosyl--1,1' N-octanoyl-D-erythro-sphingosine

Base Information

Chemical Name:D-galactosyl--1,1' N-octanoyl-D-erythro-sphingosine
CAS No.:41613-16-5
Molecular Formula:C32H61NO8
Molecular Weight:587.83
Hs Code.:
Mol file:41613-16-5.mol

Synonyms:D-galactosyl--1,1' N-octanoyl-D-erythro-sphingosine;N-octanoyl-B-D-galactosylceramide

Suppliers and Price of D-galactosyl--1,1' N-octanoyl-D-erythro-sphingosine

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

Cayman Chemical
C8 Galactosylceramide (d18:1/8:0) ≥98%
10mg
$ 375.00

American Custom Chemicals Corporation
D-GALACTOSYL-BETA-1,1'-N-OCTANOYL-D-ERYTHRO-SPHINGOSINE 95.00%
5MG
$ 499.80

Total 4 raw suppliers

Chemical Property of D-galactosyl--1,1' N-octanoyl-D-erythro-sphingosine

Chemical Property:

PSA：152.20000
LogP:5.10670

Purity/Quality:

97% ^*data from raw suppliers

C8 Galactosylceramide (d18:1/8:0) ≥98% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Description C8 Galactosylceramide is a synthetic C8 short-chain derivative of known membrane microdomain-forming sphingolipids. It increases the amount delivered and toxicity of doxorubicin in cancerous but not non-cancerous cells when incorporated into the nanoliposomal membrane of nanoliposomal-doxorubicin. C8 Galactosylceramide induces proliferation and cytokine production by splenocytes in vitro at concentrations ranging from 100-1,000 ng/ml but has no effect on natural killer T cell production in vivo. It also activates NF-κB production in C6 glioma cells when used at a concentration of 10 μM. [Matreya, LLC. Catalog No. 1334]

Technology Process of D-galactosyl--1,1' N-octanoyl-D-erythro-sphingosine

There total 1 articles about D-galactosyl--1,1' N-octanoyl-D-erythro-sphingosine 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:

: 2238-90-6,52050-17-6,56453-02-2,95119-84-9,95975-32-9,106565-70-2
psychosine

: 111-64-8
n-octanoic acid chloride

: 41613-16-5
C₃₂H₆₁NO₈

Guidance literature:: n-octanoic acid chloride; With pyridine; In 1-methyl-pyrrolidin-2-one; at 20 ℃;

psychosine; In tetrahydrofuran; at 20 ℃; Further stages.;
DOI:10.1021/ja017576o