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DL-ALPHA-AMINOPIMELIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 627-76-9 Structure
  • Basic information

    1. Product Name: DL-ALPHA-AMINOPIMELIC ACID
    2. Synonyms: DL-Heptyline DL-2-aMinoheptanedioic acid;NSC 402480;DL-a-AMinopiMelic acid, H-DL-ApM-OH;DL-a-Aminopimelic acid≥ 99% (TLC);DL-2-AMINOHEPTANEDIOIC ACID;DL-2-AMINOPIMELIC ACID;DL-2-AMINO-1,7-HEPTANEDIOIC ACID;D,L-A-AMINOPIMELIC ACID
    3. CAS NO:627-76-9
    4. Molecular Formula: C7H13NO4
    5. Molecular Weight: 175.18
    6. EINECS: 211-011-7
    7. Product Categories: Amino Acids;Amino Acids 13C, 2H, 15N;Amino Acids & Derivatives
    8. Mol File: 627-76-9.mol
  • Chemical Properties

    1. Melting Point: 223 °C (dec.)(lit.)
    2. Boiling Point: 378.5 °C at 760 mmHg
    3. Flash Point: 182.7 °C
    4. Appearance: /
    5. Density: 1.275 g/cm3
    6. Vapor Pressure: 8.95E-07mmHg at 25°C
    7. Refractive Index: 1.51
    8. Storage Temp.: Store at RT.
    9. Solubility: Methanol (Slightly, Heated), Water (Slightly)
    10. PKA: 2.52±0.24(Predicted)
    11. CAS DataBase Reference: DL-ALPHA-AMINOPIMELIC ACID(CAS DataBase Reference)
    12. NIST Chemistry Reference: DL-ALPHA-AMINOPIMELIC ACID(627-76-9)
    13. EPA Substance Registry System: DL-ALPHA-AMINOPIMELIC ACID(627-76-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 627-76-9(Hazardous Substances Data)

627-76-9 Usage

Chemical Properties

White powder

Check Digit Verification of cas no

The CAS Registry Mumber 627-76-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 627-76:
(5*6)+(4*2)+(3*7)+(2*7)+(1*6)=79
79 % 10 = 9
So 627-76-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H13NO4/c8-5(7(11)12)3-1-2-4-6(9)10/h5H,1-4,8H2,(H,9,10)(H,11,12)

627-76-9 Well-known Company Product Price

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  • TCI America

  • (A0404)  DL-2-Aminopimelic Acid  >98.0%(T)

  • 627-76-9

  • 1g

  • 855.00CNY

  • Detail

627-76-9SDS

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 DL-2-Aminopimelic Acid

1.2 Other means of identification

Product number -
Other names DL-α-AMINOPIMELIC ACID

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:627-76-9 SDS

627-76-9Relevant articles and documents

GADD45BETA TARGETING AGENTS

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, (2012/11/08)

Compounds based around tetrapeptide, tripeptide and dipeptide moeties and corresponding peptiod moeties. Related methods and pharmaceutical compositions for use in treatment of cancer, inflammatory diseases, and other disorders.

Inhibitors selective for HDAC6 in enzymes and cells

Gupta, Praveer K.,Reid, Robert C.,Liu, Ligong,Lucke, Andrew J.,Broomfield, Steve A.,Andrews, Melanie R.,Sweet, Matthew J.,Fairlie, David P.

supporting information; experimental part, p. 7067 - 7070 (2011/01/03)

Histone deacetylase inhibitors with anticancer or anti-inflammatory activity bind to Class I or Class I and II HDAC enzymes. Here we compare selectivity of inhibitors of a Class II HDAC enzyme (HDAC6) and find one that retains high selectivity in macrophages.

PREPARATION OF 6-AMINOCAPROIC ACID FROM α-KETOPIMELIC ACID

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Page/Page column 45-46, (2009/10/22)

The invention relates to a method for preparing 6-aminocaproic acid (hereinafter also referred to as '6-ACA')usinga biocatalyst. The invention further relates to a method for preparing e-caprolactam (hereafter referred to as 'caprolactam') by cyclising such 6-ACA. The invention further relates to a host cell, a micro-organism, or a polynucleotidewhich may be used inthe preparation of 6-ACA or caprolactam.

INHIBITORS OF KYNURENINE AMINOTRANSFERASE AND USES THEREFOR

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Page/Page column 21, (2008/06/13)

Provided herein are methods of decreasing a level of kynurenic acid in a cell and of treating a pathophysiological condition in a subject associated with an increase in kynurenic acid in a subject. In these methods the inhibitory action of dicarboxylic acids or derivatives or analogs thereof are effective to inhibit activity of kynurenine aminotransferase II. Also provided is a method of screening for potential inhibitory compounds for kynurenine aminotransferase II. The dicarboxylic acids or derivatives or analogs thereof may have the structural formula, where R1 is H, NH2 or NHCH3, R2 is H or CH3, n is 0 to 14, and X is -COOH, CH2OH, -PO3H2, -SO2H, or -SO3H; or a pharmacologically acceptable salt.

Peptides with an insulin-like action

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, (2008/06/13)

Peptides with an insulin-like action, of formula I: STR1 in which G is a hydrogen atom, an amino add residue, or a monosubstituted or polysubstituted amino acid; D is an amino acid residue, a phosphoamino acid residue, a monosaccharide residue, or a covalent bond; E is --NH--(CH2)n --NR52, a glycerol residue, or --NH--(CH2)p --R6 --R7 ; R1 is (C1 -C4)-alkyl or =O; R2 is a sulfhydryl protecting group, (C1 -C3)-alkyl, or a hydrogen atom; R3 and R4, independently of one another, are a hydrogen atom or methyl; R5, each being identical or different, is a hydrogen atom, 1 to 6 monosaccharide residues, or 1 to 6 monosubstituted or polysubstituted monosaccharide residues; R6 is O PO4 H, PO2 H, NHCOO, S or OCOO; R7 is a hydrogen atom, 1 to 6 monosaccharide residues, or 1 to 6 monosubstituted or polysubstituted monosaccharide residues; w is an integer 1 or 2; their preparation and use for treatment of diabetes mellitus or insulin-independent diabetes.

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