Structure

N-(4-Aminobenzoyl)-L-glutamic acid

CAS
4271-30-1
Catalog Number
ACM4271301-1
Category
Amino Acids
Molecular Weight
266.25

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Specification

Synonyms
N-(p-Aminobenzoyl)glutamic acid
SMILES
Nc1ccc(cc1)C(=O)N[C@@H](CCC(O)=O)C(O)=O
InChI
1S/C12H14N2O5/c13-8-3-1-7(2-4-8)11(17)14-9(12(18)19)5-6-10(15)16/h1-4,9H,5-6,13H2,(H,14,17)(H,15,16)(H,18,19)/t9-/m0/s1
InChI Key
GADGMZDHLQLZRI-VIFPVBQESA-N
Melting Point
175 ℃(dec.)
Application
N-(4-Aminobenzoyl)-L-glutamic acid (ABG) is used as a strong UV absorbing tag for the derivitization of oligosaccharides to enhance their detection in analytical methods such as capillary zone electrophoresis (CZE).
Assay
≥98% (TLC)
Beilstein
2816320
Biochemical Physiological Action
N-p-Aminobenzoyl)-L-glutamic acid is a folate catabolite that can be metabolized by bacterial p-aminobenzoate auxotrophs possessing the enzyme p-aminobenzoyl-glutamate hydrolase.
Color
off-white to beige
EC Number
224-261-7
Form
powder
MDL Number
MFCD00042821
NACRES
NA.26
PubChem ID
24890463
Quality Level
200
Storage Temperature
-20℃

Upstream Synthesis Route 1

  • 6758-40-3
  • 4271-30-1

Reference: [1] Patent: CN105439895, 2016, A, . Location in patent: Paragraph 0029; 0030

Upstream Synthesis Route 2

  • 233600-78-7
  • 4271-30-1

Reference: [1] Journal of the Chemical Society - Perkin Transactions 1, 1999, # 10, p. 1311 - 1323

Upstream Synthesis Route 3

  • 56-86-0
  • 4271-30-1

Reference: [1] Journal of the Chemical Society - Perkin Transactions 1, 1999, # 10, p. 1311 - 1323
[2] Journal of the Chemical Society, 1949, p. 1401,1404

Downstream Synthesis Route 1

  • 64-18-6
  • 4271-30-1
  • 93528-16-6

Reference: [1]Patent: US2740784,1954,

Downstream Synthesis Route 2

  • 1073-99-0
  • 5221-17-0
  • 4271-30-1
  • 103207-69-8

Reference: [1]Patent: US2740784,1954,

Downstream Synthesis Route 3

  • 3240-72-0
  • 5221-17-0
  • 4271-30-1
  • 25663-25-6

Reference: [1]Patent: US2478873,1947,

* For details of the synthesis route, please refer to the original source to ensure accuracy.

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