Azelaic Acid
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Azelaic acid, 98%
CAS: 123-99-9 Molecular Formula: C9H16O4 Molecular Weight (g/mol): 188.223 MDL Number: MFCD00004432 InChI Key: BDJRBEYXGGNYIS-UHFFFAOYSA-N Synonym: azelaic acid,finacea,anchoic acid,azelex,lepargylic acid,skinoren,1,7-heptanedicarboxylic acid,heptanedicarboxylic acid,1,9-nonanedioic acid,emerox 1110 PubChem CID: 2266 ChEBI: CHEBI:48131 IUPAC Name: nonanedioic acid SMILES: C(CCCC(=O)O)CCCC(=O)O
| PubChem CID | 2266 |
|---|---|
| CAS | 123-99-9 |
| Molecular Weight (g/mol) | 188.223 |
| ChEBI | CHEBI:48131 |
| MDL Number | MFCD00004432 |
| SMILES | C(CCCC(=O)O)CCCC(=O)O |
| Synonym | azelaic acid,finacea,anchoic acid,azelex,lepargylic acid,skinoren,1,7-heptanedicarboxylic acid,heptanedicarboxylic acid,1,9-nonanedioic acid,emerox 1110 |
| IUPAC Name | nonanedioic acid |
| InChI Key | BDJRBEYXGGNYIS-UHFFFAOYSA-N |
| Molecular Formula | C9H16O4 |
Azelaic acid, 96%
CAS: 123-99-9 Molecular Formula: C9H16O4 Molecular Weight (g/mol): 188.223 MDL Number: MFCD00004432 InChI Key: BDJRBEYXGGNYIS-UHFFFAOYSA-N Synonym: azelaic acid,finacea,anchoic acid,azelex,lepargylic acid,skinoren,1,7-heptanedicarboxylic acid,heptanedicarboxylic acid,1,9-nonanedioic acid,emerox 1110 PubChem CID: 2266 ChEBI: CHEBI:48131 IUPAC Name: nonanedioic acid SMILES: C(CCCC(=O)O)CCCC(=O)O
| PubChem CID | 2266 |
|---|---|
| CAS | 123-99-9 |
| Molecular Weight (g/mol) | 188.223 |
| ChEBI | CHEBI:48131 |
| MDL Number | MFCD00004432 |
| SMILES | C(CCCC(=O)O)CCCC(=O)O |
| Synonym | azelaic acid,finacea,anchoic acid,azelex,lepargylic acid,skinoren,1,7-heptanedicarboxylic acid,heptanedicarboxylic acid,1,9-nonanedioic acid,emerox 1110 |
| IUPAC Name | nonanedioic acid |
| InChI Key | BDJRBEYXGGNYIS-UHFFFAOYSA-N |
| Molecular Formula | C9H16O4 |
Azelaic acid, tech. 80%
CAS: 123-99-9 Molecular Formula: C9H16O4 Molecular Weight (g/mol): 188.223 MDL Number: MFCD00004432 InChI Key: BDJRBEYXGGNYIS-UHFFFAOYSA-N Synonym: azelaic acid,finacea,anchoic acid,azelex,lepargylic acid,skinoren,1,7-heptanedicarboxylic acid,heptanedicarboxylic acid,1,9-nonanedioic acid,emerox 1110 PubChem CID: 2266 ChEBI: CHEBI:48131 IUPAC Name: nonanedioic acid SMILES: C(CCCC(=O)O)CCCC(=O)O
| PubChem CID | 2266 |
|---|---|
| CAS | 123-99-9 |
| Molecular Weight (g/mol) | 188.223 |
| ChEBI | CHEBI:48131 |
| MDL Number | MFCD00004432 |
| SMILES | C(CCCC(=O)O)CCCC(=O)O |
| Synonym | azelaic acid,finacea,anchoic acid,azelex,lepargylic acid,skinoren,1,7-heptanedicarboxylic acid,heptanedicarboxylic acid,1,9-nonanedioic acid,emerox 1110 |
| IUPAC Name | nonanedioic acid |
| InChI Key | BDJRBEYXGGNYIS-UHFFFAOYSA-N |
| Molecular Formula | C9H16O4 |
Azelaic acid, 98%
CAS: 123-99-9 Molecular Formula: C9H16O4 Molecular Weight (g/mol): 188.223 MDL Number: MFCD00004432 InChI Key: BDJRBEYXGGNYIS-UHFFFAOYSA-N Synonym: azelaic acid,finacea,anchoic acid,azelex,lepargylic acid,skinoren,1,7-heptanedicarboxylic acid,heptanedicarboxylic acid,1,9-nonanedioic acid,emerox 1110 PubChem CID: 2266 ChEBI: CHEBI:48131 IUPAC Name: nonanedioic acid SMILES: C(CCCC(=O)O)CCCC(=O)O
| PubChem CID | 2266 |
|---|---|
| CAS | 123-99-9 |
| Molecular Weight (g/mol) | 188.223 |
| ChEBI | CHEBI:48131 |
| MDL Number | MFCD00004432 |
| SMILES | C(CCCC(=O)O)CCCC(=O)O |
| Synonym | azelaic acid,finacea,anchoic acid,azelex,lepargylic acid,skinoren,1,7-heptanedicarboxylic acid,heptanedicarboxylic acid,1,9-nonanedioic acid,emerox 1110 |
| IUPAC Name | nonanedioic acid |
| InChI Key | BDJRBEYXGGNYIS-UHFFFAOYSA-N |
| Molecular Formula | C9H16O4 |
Cayman Chemical Azelaic Acid, Purity: ≥95%, CAS: 123-99-9, 250 g
A dicarboxylic acid with diverse biological activities; a competitive inhibitor of tyrosinase, NADH dehydrogenase, succinic dehydrogenase, and reduced ubiquitinone:cytochrome C oxidoreductase in vitro; inhibits the growth and colony formation of B16 murine as well as HMB2 and SK32 human melanoma cells; decreases DNA synthesis, induces mitochondrial damage and dilation of the RER, and reduces growth of mouse keratinocytes; bacteriostatic against various microorganisms (MICs = 0.03-0.25 M)
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Cayman Chemical Azelaic Acid, Purity: ≥95%, CAS: 123-99-9, 50 g
A dicarboxylic acid with diverse biological activities; a competitive inhibitor of tyrosinase, NADH dehydrogenase, succinic dehydrogenase, and reduced ubiquitinone:cytochrome C oxidoreductase in vitro; inhibits the growth and colony formation of B16 murine as well as HMB2 and SK32 human melanoma cells; decreases DNA synthesis, induces mitochondrial damage and dilation of the RER, and reduces growth of mouse keratinocytes; bacteriostatic against various microorganisms (MICs = 0.03-0.25 M)
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Cayman Chemical Azelaic Acid, Purity: ≥95%, CAS: 123-99-9, 100 g
A dicarboxylic acid with diverse biological activities; a competitive inhibitor of tyrosinase, NADH dehydrogenase, succinic dehydrogenase, and reduced ubiquitinone:cytochrome C oxidoreductase in vitro; inhibits the growth and colony formation of B16 murine as well as HMB2 and SK32 human melanoma cells; decreases DNA synthesis, induces mitochondrial damage and dilation of the RER, and reduces growth of mouse keratinocytes; bacteriostatic against various microorganisms (MICs = 0.03-0.25 M)
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Cayman Chemical Azelaic Acid, Purity: ≥95%, CAS: 123-99-9, 25 g
A dicarboxylic acid with diverse biological activities; a competitive inhibitor of tyrosinase, NADH dehydrogenase, succinic dehydrogenase, and reduced ubiquitinone:cytochrome C oxidoreductase in vitro; inhibits the growth and colony formation of B16 murine as well as HMB2 and SK32 human melanoma cells; decreases DNA synthesis, induces mitochondrial damage and dilation of the RER, and reduces growth of mouse keratinocytes; bacteriostatic against various microorganisms (MICs = 0.03-0.25 M)
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AdipoGen Azelaic acid dichloride
Chemical. CAS 123-98-8. Formula C9H14Cl2O2. MW 225.11. Azelaic acid dichloride is a bulding block for synthesis e.g. copolymers. It is the diacid chloride derivative of azelaic acid.
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Selleck Chemical LLC Azelaic acid S4550-100mg
Azelaic acid (Nonanedioic acid Finacea Azelex Anchoic acid) is an organic compound produced by the ozonolysis of oleic acid and possesses antibacterial keratolytic comedolytic and anti-oxidant activity
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