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DL-ALANINE (3-13C) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 131157-42-1 Structure
  • Basic information

    1. Product Name: DL-ALANINE (3-13C)
    2. Synonyms: DL-ALANINE (3-13C);DL-ALANINE-3-13C, 99 ATOM % 13C;2-D, 96%)
    3. CAS NO:131157-42-1
    4. Molecular Formula: C3H7NO2
    5. Molecular Weight: 90.1
    6. EINECS: N/A
    7. Product Categories: Amino Acids 13C, 2H, 15N;A;Alphabetical Listings;Stable Isotopes
    8. Mol File: 131157-42-1.mol
  • Chemical Properties

    1. Melting Point: 289 °C (dec.)(lit.)
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: DL-ALANINE (3-13C)(CAS DataBase Reference)
    10. NIST Chemistry Reference: DL-ALANINE (3-13C)(131157-42-1)
    11. EPA Substance Registry System: DL-ALANINE (3-13C)(131157-42-1)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 131157-42-1(Hazardous Substances Data)

131157-42-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 131157-42-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,1,5 and 7 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 131157-42:
(8*1)+(7*3)+(6*1)+(5*1)+(4*5)+(3*7)+(2*4)+(1*2)=91
91 % 10 = 1
So 131157-42-1 is a valid CAS Registry Number.

131157-42-1SDS

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 3-13C alanine

1.2 Other means of identification

Product number -
Other names L-<3-13C>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:131157-42-1 SDS

131157-42-1Relevant articles and documents

An asymmetric synthesis of L-[3-13C]alanine

Takatori, Kazuhiko,Toyama, Sanae,Narumi, Shoko,Fujii, Seishiro,Kajiwara, Masahiro

, p. 91 - 94 (2004)

L-[3-13C]Alanine was synthesized from [13C]methyl iodide by using Dellaria's oxazinone, prepared from phenyl[2- 13C]bromoacetate and (S)-2-phenylglycinol, as a chiral glycine equivalent. Alkylation of the oxazinone with [13C]methyl iodide was achieved with high diastereoselectivity. Hydrolysis and removal of the chiral auxiliary of the alkylated oxazinone gave L-[3-13C]alanine. Copyright

The metabolic and biochemical impact of glucose 6-sulfonate (sulfoquinovose), a dietary sugar, on carbohydrate metabolism

Sacoman, Juliana L.,Badish, Lauren N.,Sharkey, Thomas D.,Hollingsworth, Rawle I.

, p. 21 - 29,9 (2012/12/12)

Increased activity of the main carbohydrate pathways (glycolysis, pentose phosphate, and hexosamine biosynthetic pathways) is one of the hallmarks of metabolic diseases such as cancer. Sulfoquinovosyl diacylglycerol is a sulfoglycolipid found in the human

The metabolic and biochemical impact of glucose 6-sulfonate (sulfoquinovose), a dietary sugar, on carbohydrate metabolism

Sacoman, Juliana L.,Badish, Lauren N.,Sharkey, Thomas D.,Hollingsworth, Rawle I.

, p. 21 - 29 (2013/01/15)

Increased activity of the main carbohydrate pathways (glycolysis, pentose phosphate, and hexosamine biosynthetic pathways) is one of the hallmarks of metabolic diseases such as cancer. Sulfoquinovosyl diacylglycerol is a sulfoglycolipid found in the human

Multi-enzymatic Synthesis of β-11C-Labelled L-Tyrosine and L-DOPA

Bjurling, Peter,Watanabe, Yasuyoshi,Oka, Shogo,Nagasawa, Toru,Yamada, Hideaki,Langstroem, Bengt

, p. 183 - 188 (2007/10/02)

The synthesis of L-tyrosine (3) and L-DOPA (4) from carbon dioxide via DL-alanine (1) using a combination of organic synthetic methods and a multi-enzymatic procedure are presented.The 11C-labelled alanine was prepared by a methy

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