1,9-NONANEDIOIC-D14 ACID

Base Information

Chemical Name:1,9-NONANEDIOIC-D14 ACID
CAS No.:119176-67-9
Molecular Formula:C₉H₁₆O₄
Molecular Weight:202.112
Hs Code.:
Mol file:119176-67-9.mol

Synonyms:1,9-NONANEDIOIC-D14 ACID

Suppliers and Price of 1,9-NONANEDIOIC-D14 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
Nonanedioic-D14 Acid
10mg
$ 403.00

TRC
Nonanedioic-D14Acid
100mg
$ 545.00

Medical Isotopes, Inc.
1,9-Nonanedioic-d14acid
1 mg
$ 190.00

American Custom Chemicals Corporation
1,9-NONANEDIOIC-D14 ACID 95.00%
5MG
$ 501.05

Total 5 raw suppliers

Chemical Property of 1,9-NONANEDIOIC-D14 ACID

Chemical Property:

PSA：74.60000
LogP:1.88630
Storage Temp.:Refrigerator
Solubility.:DMSO (Slightly), Methanol (Slightly)

Purity/Quality:

99%, ^*data from raw suppliers

Nonanedioic-D14 Acid ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses Nonanedioic-D14 acid is a labelled analogue of Nonanedioic acid, a bioactive molecule used in treating acne and other skin disorders.

Technology Process of 1,9-NONANEDIOIC-D14 ACID

There total 1 articles about 1,9-NONANEDIOIC-D14 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: 74.0%

: 123-99-9,26776-28-3
azelaic acid

: 69974-55-6
[2H₁₅]-n-octanoic acid

: 119176-67-9
[D₁₄]azelaic acid

Guidance literature:: With [D]-sodium hydroxide; 10% Pt/activated carbon; water-d2; at 220 ℃; for 144h; under 17251.7 Torr; Inert atmosphere; Autoclave;
DOI:10.1002/jlcr.3088

Reference yield:

: 119176-67-9
[D₁₄]azelaic acid

: 1466552-35-1
[D₁₄]9-carbomethoxynonyl-triphenylphosphonium bromide

Guidance literature:: Multi-step reaction with 6 steps

1: sulfuric acid / 48 h / Inert atmosphere; Reflux

2: barium hydroxide octahydrate / methanol / 24 h / 20 °C

3: hydrogenchloride; water / pH Ca_. 1

4: dimethylsulfide borane complex / tetrahydrofuran / 20 h / 0 - 20 °C / Inert atmosphere

5: triphenylphosphine; bromine; pyridine / dichloromethane / 2.5 h / 0 - 20 °C / Inert atmosphere

6: toluene / 68 h / 120 °C / Schlenk technique; Inert atmosphere

With pyridine; hydrogenchloride; barium hydroxide octahydrate; dimethylsulfide borane complex; sulfuric acid; water; bromine; triphenylphosphine; In tetrahydrofuran; methanol; dichloromethane; toluene;
DOI:10.1002/jlcr.3088