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10183-34-3

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10183-34-3 Usage

Biochem/physiol Actions

L-Alanine has wide range of applications as food additive and as a component in infusion solutions. It is also used as a precursor for chemical and pharmaceutical products. In a penta-alanine system, resampling helps to increase the efficacy of a “fast-switch” equilibrium sampling protocol.

Check Digit Verification of cas no

The CAS Registry Mumber 10183-34-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,8 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 10183-34:
(7*1)+(6*0)+(5*1)+(4*8)+(3*3)+(2*3)+(1*4)=63
63 % 10 = 3
So 10183-34-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H27N5O6/c1-6(16)11(21)17-7(2)12(22)18-8(3)13(23)19-9(4)14(24)20-10(5)15(25)26/h6-10H,16H2,1-5H3,(H,17,21)(H,18,22)(H,19,23)(H,20,24)(H,25,26)/t6-,7?,8?,9-,10-/m1/s1

10183-34-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name H-Ala-Ala-Ala-Ala-Ala-OH

1.2 Other means of identification

Product number -
Other names D-Penta-L-Alanine

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:10183-34-3 SDS

10183-34-3Downstream Products

10183-34-3Relevant articles and documents

Mechanism study on the oligomerization of amino acids into peptides by phosphorus trichloride

Zhao, Wenjie,Zhao, Dongxin,Lu, Kui

scheme or table, p. 691 - 698 (2009/05/07)

As treated by phosphorus trichloride, amino acids could oligomerize into polypeptides. Based on the results obtained by 31P-NMR and ESI-MS/MS, a possible reaction mechanism was proposed. The mechanism might undergo a penta-coordinated phosphorus intermediat. The activated amino acid was a five-membered cyclic penta-coordinated phosphorus intermediate. The nucleophilic attack of the amino group from an amino acid or peptide on the carbonyl group of intermediate led to the formation of peptide and released one equivalent dichloride phosphoric acid. The repetition of the reaction sequence generated a series of oligopeptides. Copyright Taylor & Francis Group, LLC.

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