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26982-21-8

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26982-21-8 Usage

Uses

Poly-L-ornithine hydrochloride has been used as a substrate analog of acetyl-poly-L-lysine to study substrate binding and catalysis of the NAD-dependent protein deacetylase Hst2. It has been used to bind alginate-polycation-alginate (APA) microcapsules.

Biochem/physiol Actions

Poly-L-ornithine is a polycationic synthetic amino acid polymer. It boosts nasal absorption of hydrophilic macromolecular drugs. Poly-L-ornithine is a specialized coating that acts as a charge modifier.

Check Digit Verification of cas no

The CAS Registry Mumber 26982-21-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,9,8 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 26982-21:
(7*2)+(6*6)+(5*9)+(4*8)+(3*2)+(2*2)+(1*1)=138
138 % 10 = 8
So 26982-21-8 is a valid CAS Registry Number.

26982-21-8 Well-known Company Product Price

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  • Sigma

  • (P2533)  Poly-L-ornithinehydrochloride  mol wt 15,000-30,000

  • 26982-21-8

  • P2533-10MG

  • 709.02CNY

  • Detail
  • Sigma

  • (P2533)  Poly-L-ornithinehydrochloride  mol wt 15,000-30,000

  • 26982-21-8

  • P2533-50MG

  • 2,128.23CNY

  • Detail
  • Sigma

  • (P2533)  Poly-L-ornithinehydrochloride  mol wt 15,000-30,000

  • 26982-21-8

  • P2533-100MG

  • 3,546.27CNY

  • Detail
  • Sigma

  • (P2533)  Poly-L-ornithinehydrochloride  mol wt 15,000-30,000

  • 26982-21-8

  • P2533-500MG

  • 14,180.40CNY

  • Detail

26982-21-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name L-Ornithine hydrochloride (1:1)

1.2 Other means of identification

Product number -
Other names Tetrahydro-4-methyl-2-phenyl-2H-pyran

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:26982-21-8 SDS

26982-21-8Relevant articles and documents

Highly enantioselective synthesis of non-natural aliphatic α-amino acids via asymmetric hydrogenation

Ji, Jianjian,Chen, Caiyou,Cai, Jiayu,Wang, Xinrui,Zhang, Kai,Shi, Liyang,Lv, Hui,Zhang, Xumu

supporting information, p. 7624 - 7627 (2015/07/15)

By employing a rhodium-Duanphos complex as the catalyst, β-alkyl (Z)-N-acetyldehydroamino esters were smoothly hydrogenated in a highly efficient and enantioselective way. Excellent enantioselectivities together with excellent yields were achieved for a series of substrates. An efficient approach for the synthesis of the intermediate of the orally administered anti-diabetic drugs Alogliptin and Linagliptin in the DPP-4 inhibitor class was also developed.

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