1198-84-1,MFCD00004234
Catalog No.:AA000PLU

1198-84-1 | 2-Hydroxy-2-(4-hydroxyphenyl)acetic acid

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
98% +(Loss on drying≤10%)
in stock  
$6.00   $4.00
- +
1g
98% +(Loss on drying≤10%)
in stock  
$7.00   $5.00
- +
5g
98% +(Loss on drying≤10%)
in stock  
$11.00   $8.00
- +
25g
98%
in stock  
$49.00   $34.00
- +
100g
98%
in stock  
$137.00   $96.00
- +
500g
98%
in stock  
$502.00 $352.00
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA000PLU
Chemical Name:
2-Hydroxy-2-(4-hydroxyphenyl)acetic acid
CAS Number:
1198-84-1
Molecular Formula:
C8H8O4
Molecular Weight:
168.1467
MDL Number:
MFCD00004234
SMILES:
OC(=O)C(c1ccc(cc1)O)O
Properties
Computed Properties
 
Complexity:
160  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
3  
Rotatable Bond Count:
2  
Undefined Atom Stereocenter Count:
1  
XLogP3:
0.3  

Literature

Title: Halicloic acids A and B isolated from the marine sponge Haliclona sp. collected in the Philippines inhibit indoleamine 2,3-dioxygenase.

Journal: Journal of natural products 20120824

Title: A public resource for metabolic pathway mapping of Aspergillus fumigatus Af293.

Journal: Medical mycology 20110401

Title: Metabolic engineering of the L-phenylalanine pathway in Escherichia coli for the production of S- or R-mandelic acid.

Journal: Microbial cell factories 20110101

Title: The metabolic fate of red wine and grape juice polyphenols in humans assessed by metabolomics.

Journal: Molecular nutrition & food research 20100701

Title: The rate-limiting catalytic steps of hydroxymandelate synthase from Amycolatopsis orientalis.

Journal: Biochemistry 20100309

Title: Investigation into the mechanism of phenolic couplings during the biosynthesis of glycopeptide antibiotics.

Journal: Chembiochem : a European journal of chemical biology 20080922

Title: Two roads diverged: the structure of hydroxymandelate synthase from Amycolatopsis orientalis in complex with 4-hydroxymandelate.

Journal: Biochemistry 20080219

Title: The genome of the versatile nitrogen fixer Azorhizobium caulinodans ORS571.

Journal: BMC genomics 20080101

Title: Adaptogenic and nootropic activities of aqueous extract of Vitis vinifera (grape seed): an experimental study in rat model.

Journal: BMC complementary and alternative medicine 20050101

Title: Engineering p-hydroxyphenylpyruvate dioxygenase to a p-hydroxymandelate synthase and evidence for the proposed benzene oxide intermediate in homogentisate formation.

Journal: Biochemistry 20040127

Title: Improved chemical strategies for the targeted therapy of cancer.

Journal: Angewandte Chemie (International ed. in English) 20031013

Title: Structure, biosynthetic origin, and engineered biosynthesis of calcium-dependent antibiotics from Streptomyces coelicolor.

Journal: Chemistry & biology 20021101

Title: Li FF, et al. Engineering Escherichia coli for production of 4-hydroxymandelic acid using glucose-xylosemixture. Microb Cell Fact. 2016 May 27;15:90.

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SDS
Tags:1198-84-1 Molecular Formula|1198-84-1 MDL|1198-84-1 SMILES|1198-84-1 2-Hydroxy-2-(4-hydroxyphenyl)acetic acid
Catalog No.: AA000PLU
1198-84-1,MFCD00004234
1198-84-1 | 2-Hydroxy-2-(4-hydroxyphenyl)acetic acid
Pack Size: 250mg
Purity: 98% +(Loss on drying≤10%)
in stock
$6.00 $4.00
Pack Size: 1g
Purity: 98% +(Loss on drying≤10%)
in stock
$7.00 $5.00
Pack Size: 5g
Purity: 98% +(Loss on drying≤10%)
in stock
$11.00 $8.00
Pack Size: 25g
Purity: 98%
in stock
$49.00 $34.00
Pack Size: 100g
Purity: 98%
in stock
$137.00 $96.00
Pack Size: 500g
Purity: 98%
in stock
$502.00 $352.00
Quantity
- +
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bulk Quotation Request
Technical Information
Catalog Number: AA000PLU
Chemical Name: 2-Hydroxy-2-(4-hydroxyphenyl)acetic acid
CAS Number: 1198-84-1
Molecular Formula: C8H8O4
Molecular Weight: 168.1467
MDL Number: MFCD00004234
SMILES: OC(=O)C(c1ccc(cc1)O)O
Properties
Complexity: 160  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 12  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 3  
Rotatable Bond Count: 2  
Undefined Atom Stereocenter Count: 1  
XLogP3: 0.3  
Literature fold

Title: Halicloic acids A and B isolated from the marine sponge Haliclona sp. collected in the Philippines inhibit indoleamine 2,3-dioxygenase.

Journal: Journal of natural products20120824

Title: A public resource for metabolic pathway mapping of Aspergillus fumigatus Af293.

Journal: Medical mycology20110401

Title: Metabolic engineering of the L-phenylalanine pathway in Escherichia coli for the production of S- or R-mandelic acid.

Journal: Microbial cell factories20110101

Title: The metabolic fate of red wine and grape juice polyphenols in humans assessed by metabolomics.

Journal: Molecular nutrition & food research20100701

Title: The rate-limiting catalytic steps of hydroxymandelate synthase from Amycolatopsis orientalis.

Journal: Biochemistry20100309

Title: Investigation into the mechanism of phenolic couplings during the biosynthesis of glycopeptide antibiotics.

Journal: Chembiochem : a European journal of chemical biology20080922

Title: Two roads diverged: the structure of hydroxymandelate synthase from Amycolatopsis orientalis in complex with 4-hydroxymandelate.

Journal: Biochemistry20080219

Title: The genome of the versatile nitrogen fixer Azorhizobium caulinodans ORS571.

Journal: BMC genomics20080101

Title: Adaptogenic and nootropic activities of aqueous extract of Vitis vinifera (grape seed): an experimental study in rat model.

Journal: BMC complementary and alternative medicine20050101

Title: Engineering p-hydroxyphenylpyruvate dioxygenase to a p-hydroxymandelate synthase and evidence for the proposed benzene oxide intermediate in homogentisate formation.

Journal: Biochemistry20040127

Title: Improved chemical strategies for the targeted therapy of cancer.

Journal: Angewandte Chemie (International ed. in English)20031013

Title: Structure, biosynthetic origin, and engineered biosynthesis of calcium-dependent antibiotics from Streptomyces coelicolor.

Journal: Chemistry & biology20021101

Title: Li FF, et al. Engineering Escherichia coli for production of 4-hydroxymandelic acid using glucose-xylosemixture. Microb Cell Fact. 2016 May 27;15:90.

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