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1878-49-5,MFCD00014354
Catalog No.:AA002GFF

1878-49-5 | (2-Methylphenoxy)acetic acid

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Purity
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1g
98%
in stock  
$14.00   $10.00
- +
5g
98%(GC)
in stock  
$31.00   $22.00
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25g
98%
in stock  
$127.00   $89.00
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100g
98%(GC)
in stock  
$381.00   $267.00
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  • Technical Information
  • Properties
  • Literature
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA002GFF
Chemical Name:
(2-Methylphenoxy)acetic acid
CAS Number:
1878-49-5
Molecular Formula:
C9H10O3
Molecular Weight:
166.1739
MDL Number:
MFCD00014354
SMILES:
OC(=O)COc1ccccc1C
NSC Number:
5293
Properties
Properties
 
BP:
288.4°C at 760 mmHg  
Form:
Solid  
MP:
155-157 °C(lit.)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
156  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
3  
XLogP3:
2  

Literature

Title: Tris-2(hydroxyethyl)ammonium (2-methylphenoxy)acetate as an inhibitor of synthesis of acid phospholipase A2 of mononuclear cells.

Journal: Doklady. Biochemistry and biophysics 20120101

Title: The complex of zinc bis-(2-methylphenoxyacetate) with tris-2(hydroxyethyl) amine as an activator of synthesis of total tryptophanyl-tRNA synthetase.

Journal: Doklady. Biochemistry and biophysics 20120101

Title: Tris-2(hydroxyethyl)ammonium 2-methylphenoxyacetate activates the synthesis of mRNA aminoacyl-tRNA synthetase.

Journal: Doklady. Biochemistry and biophysics 20110101

Title: Tris-2(hydroxyethyl) ammonium 2-methylphenoxyacetate as an activator of aorta intima acid lipase.

Journal: Doklady. Biochemistry and biophysics 20110101

Title: Tris-2(hydroxyethyl) ammonium 2-methylphenoxyacetate as an inhibitor of synthesis of liver phospholipase A1.

Journal: Doklady. Biochemistry and biophysics 20110101

Title: Tris-2(hydroxyethyl)ammonium (2-methylphenoxy)acetate as an inhibitor of synthesis of acid cholesterol esterase of platelets and mononuclear cells.

Journal: Doklady. Biochemistry and biophysics 20110101

Title: Identification of auxins by a chemical genomics approach.

Journal: Journal of experimental botany 20080701

Title: Structural Development Studies of Subtype-Selective Ligands for Peroxisome Proliferator-Activated Receptors (PPARs) Based on the 3,4-Disubstituted Phenylpropanoic Acid Scaffold as a Versatile Template.

Journal: PPAR research 20080101

Title: Oxidation of MCPA and 2,4-D by UV radiation, ozone, and the combinations UV/H2O2 and O3/H2O2.

Journal: Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes 20040501

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Tags:1878-49-5 Molecular Formula|1878-49-5 MDL|1878-49-5 SMILES|1878-49-5 (2-Methylphenoxy)acetic acid