Alanosine

Base Information Edit

Chemical Name:Alanosine
CAS No.:5854-93-3
Molecular Formula:C3H7 N3 O4
Molecular Weight:149.106
Hs Code.:
Mol file:5854-93-3.mol

Synonyms:Propionicacid, 2-amino-3-(hydroxynitrosamino)-, L- (8CI); Alanosine;L-2-Amino-3-(N-nitroso)hydroxylaminopropionic acid; L-2-Amino-3-(hydroxynitrosamino)propionicacid; L-Alanosine; NSC 153353; NSC 529469; SDX 102

Suppliers and Price of Alanosine

Supply Marketing:Edit

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
L-Alanosine
5mg
$ 446.00

TRC
L-Alanosine
10mg
$ 265.00

Medical Isotopes, Inc.
L-Alanosine
25 mg
$ 2120.00

Medical Isotopes, Inc.
L-Alanosine
5 mg
$ 890.00

Cayman Chemical
L-Alanosine ≥95%
25mg
$ 641.00

Cayman Chemical
L-Alanosine ≥95%
10mg
$ 276.00

Cayman Chemical
L-Alanosine ≥95%
1mg
$ 33.00

Cayman Chemical
L-Alanosine ≥95%
5mg
$ 147.00

Biosynth Carbosynth
L-Alanosine
2 mg
$ 140.00

Biosynth Carbosynth
L-Alanosine
1 mg
$ 87.50

Total 20 raw suppliers

Chemical Property of Alanosine Edit

Chemical Property:

Vapor Pressure:7.16E-07mmHg at 25°C
Melting Point:1900C (dec.)
Refractive Index:1.4900 (estimate)
Boiling Point:366.9°Cat760mmHg
PKA:4.8(at 25℃)
Flash Point:175.7°C
PSA：116.22000
Density:1.81g/cm³
LogP:-0.52880
Storage Temp.:-20°C Freezer
Solubility.:Aqueous Acid, Aqueous Base

Purity/Quality:

99%, ^*data from raw suppliers

L-Alanosine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses Antibiotic substance from the fermentation of Streptomyces alanosinicus. The first natural product found to have a N-nitrosohydroxylamino group on an aliphatic chain. An experimental insect reproduction inhibitor L-Alanosine is an antitumor antibiotic substance from the fermentation of Streptomyces alanosinicus. It is the first natural product found to have a N-nitrosohydroxylamino group on an aliphatic chain. It is also an experimental insect reproduction inhibitor.
Therapeutic Function Antineoplastic

Technology Process of Alanosine

There total 2 articles about Alanosine 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: 82.0%

: 832090-73-0,1286490-16-1
(S)-3-[nitroso(phenylmethyloxy)amino]-N-[(phenylmethyloxy)carbonyl]alanine

: 5854-93-3
Alanosine

Guidance literature:: With sodium hydroxide; hydrogen; palladium on activated charcoal; In water; at 30 ℃; for 24h; under 3750.3 Torr;
DOI:10.1002/ejoc.200400508