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609-36-9

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609-36-9 Usage

Chemical Properties

white to off-white crystalline powder

Uses

DL-Proline is the racemic mixture of both L-Proline (P755995) and D-Proline (P755990).

Definition

ChEBI: An alpha-amino acid that is pyrrolidine bearing a carboxy substituent at position 2.

Check Digit Verification of cas no

The CAS Registry Mumber 609-36-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,0 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 609-36:
(5*6)+(4*0)+(3*9)+(2*3)+(1*6)=69
69 % 10 = 9
So 609-36-9 is a valid CAS Registry Number.
InChI:InChI=1/C5H9NO2/c7-5(8)4-2-1-3-6-4/h4,6H,1-3H2,(H,7,8)

609-36-9 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (P0480)  DL-Proline  >99.0%(T)

  • 609-36-9

  • 1g

  • 150.00CNY

  • Detail
  • TCI America

  • (P0480)  DL-Proline  >99.0%(T)

  • 609-36-9

  • 5g

  • 360.00CNY

  • Detail
  • TCI America

  • (P0480)  DL-Proline  >99.0%(T)

  • 609-36-9

  • 25g

  • 890.00CNY

  • Detail
  • Alfa Aesar

  • (A13137)  DL-Proline, 99%   

  • 609-36-9

  • 5g

  • 375.0CNY

  • Detail
  • Alfa Aesar

  • (A13137)  DL-Proline, 99%   

  • 609-36-9

  • 25g

  • 1684.0CNY

  • Detail
  • Alfa Aesar

  • (A13137)  DL-Proline, 99%   

  • 609-36-9

  • 100g

  • 5877.0CNY

  • Detail
  • Vetec

  • (V900712)  DL-Proline  Vetec reagent grade, 98%

  • 609-36-9

  • V900712-5G

  • 59.67CNY

  • Detail
  • Vetec

  • (V900712)  DL-Proline  Vetec reagent grade, 98%

  • 609-36-9

  • V900712-25G

  • 92.43CNY

  • Detail
  • Aldrich

  • (171824)  DL-Proline  ReagentPlus®, 99%

  • 609-36-9

  • 171824-1G

  • 205.92CNY

  • Detail
  • Aldrich

  • (171824)  DL-Proline  ReagentPlus®, 99%

  • 609-36-9

  • 171824-5G

  • 476.19CNY

  • Detail
  • Aldrich

  • (171824)  DL-Proline  ReagentPlus®, 99%

  • 609-36-9

  • 171824-25G

  • 1,751.49CNY

  • Detail

609-36-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name proline

1.2 Other means of identification

Product number -
Other names (RS)-Proline

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:609-36-9 SDS

609-36-9Relevant articles and documents

MODIFIED INTERLEUKIN-7 PROTEINS AND USES THEREOF

-

, (2021/10/22)

Provided are a modified IL-7 polypeptide and a fusion protein containing the modified IL-7 polypeptide. The fusion protein of the modified IL-7 includes: a first domain containing an interleukin-7 polypeptide; a second domain containing an oligopeptide having 1 to 10 amino acid residues (with proviso that the second domain excludes the oligopeptide consisting of methionine and/or glycine); and (c) a third domain which prolongs the half-life of the IL-7 fusion protein. The modified IL-7 polypeptide is composed of the (a) first domain and the (b) second domain. The modified IL-7 polypeptide and the fusion protein are expressed in a higher yield than the wild-type IL-7 and shows increased stability.

Dudawalamides A-D, Antiparasitic Cyclic Depsipeptides from the Marine Cyanobacterium Moorea producens

Almaliti, Jehad,Malloy, Karla L.,Glukhov, Evgenia,Spadafora, Carmenza,Gutiérrez, Marcelino,Gerwick, William H.

, p. 1827 - 1836 (2017/06/28)

A family of 2,2-dimethyl-3-hydroxy-7-octynoic acid (Dhoya)-containing cyclic depsipeptides, named dudawalamides A-D (1-4), was isolated from a Papua New Guinean field collection of the cyanobacterium Moorea producens using bioassay-guided and spectroscopic approaches. The planar structures of dudawalamides A-D were determined by a combination of 1D and 2D NMR experiments and MS analysis, whereas the absolute configurations were determined by X-ray crystallography, modified Marfey's analysis, chiral-phase GCMS, and chiral-phase HPLC. Dudawalamides A-D possess a broad spectrum of antiparasitic activity with minimal mammalian cell cytotoxicity. Comparative analysis of the Dhoya-containing class of lipopeptides reveals intriguing structure-activity relationship features of these NRPS-PKS-derived metabolites and their derivatives.

METHODS FOR TREATING MUSCLE SPECIFIC RECEPTOR KINASE MYASTHENIA GRAVIS

-

, (2015/05/13)

Agents, compositions, and medicaments that reduce interactions between muscle specific kinase receptor (MuSK) and pathogenic immunoglobulin G4 (IgG4) antibodies specific for the first Ig-like domain of MuSK and methods and uses thereof to reduce such interactions are encompassed herein. Also encompassed are screening assays to identify inhibitors of these pathogenic antibodies, particularly those that reduce binding to MuSK. Agents identified using the screening assays described herein are envisioned for use as therapeutics, alone or in compositions or in medicaments, to improve motor function in subjects afflicted MuSK-MG.

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