ChemicalBook--->CAS DataBase List--->4271-30-1

4271-30-1

4271-30-1 Structure

4271-30-1 Structure
IdentificationMore
[Name]

N-(4-Aminobenzoyl)-L-glutamic acid
[CAS]

4271-30-1
[Synonyms]

4-AMINOBENZOIC GLUTAMIC ACID
4-AMINOBENZOYLGLUTAMIC ACID
H-4-ABZ-GLU-OH
N-(4-AMINOBENZOYL)-L-GLUTAMIC ACID
N-(P-AMINOBENZOYL)-L-GLUTAMIC ACID
P-AMINO BENZAMIDE GLUTAMIC ACID
P-AMINOBENZOYL-L-GLUTAMIC ACID
4-aminobenzoyl-L-glutamic acid
N-(4-Aminobenzoyl)-L-Glutaminic Acid
N-(4-AMINOBENZOYL)GLUTAMIC ACID
L-Glutamic acid, N-(4-aminobenzoyl)-
N-(p-Aminobenzoyl)glutamic acid
[EINECS(EC#)]

224-261-7
[Molecular Formula]

C12H14N2O5
[MDL Number]

MFCD00042821
[Molecular Weight]

266.25
[MOL File]

4271-30-1.mol
Chemical PropertiesBack Directory
[Melting point ]

~175 °C (dec.)
[alpha ]

-15 º (c=2% in 0.1N HCl)
[Boiling point ]

409.45°C (rough estimate)
[density ]

1.2846 (rough estimate)
[refractive index ]

1.6660 (estimate)
[storage temp. ]

−20°C
[solubility ]

Aqueous Base (Sparingly), Aqueous Acid (Sparingly), DMSO (Sparingly)
[form ]

neat
[pka]

3.50±0.10(Predicted)
[color ]

White to Light Beige Waxy to
[Merck ]

426
[BRN ]

2816320
[Stability:]

Hygroscopic
[Major Application]

detection
peptide synthesis
[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
[InChIKey]

GADGMZDHLQLZRI-VIFPVBQESA-N
[SMILES]

Nc1ccc(cc1)C(=O)N[C@@H](CCC(O)=O)C(O)=O
[CAS DataBase Reference]

4271-30-1(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P271-P280
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
[WGK Germany ]

3
[HS Code ]

2924296000
[Storage Class]

11 - Combustible Solids
Raw materials And Preparation ProductsBack Directory
[Raw materials]

4-Nitrobenzoic acid-->4-Nitrobenzoyl chloride-->Ammonium sulfide-->P-NITROBENZOYL-L-GLUTAMIC ACID-->Activated carbon-->Ammonium formate-->Methanol-->Palladium
[Preparation Products]

Aminopterin-->Folic acid
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

N-(4-Aminobenzoyl)-L-glutamic acid(4271-30-1).msds
Hazard InformationBack Directory
[Chemical Properties]

Light Tan Waxy Solid
[Uses]

Major metabolite of 5-Methyltetrahydrofolic Acid
[Uses]

Marker in folate metabolism studies.
[Definition]

ChEBI: A dipeptide resulting from the formal condensation of the carboxylic acid group of 4-aminobenzoic acid with the amino group of L-glutamic acid.
[Biological Activity]

N-p-Aminobenzoyl)-L-glutamic acid is a folate catabolite th at can be metabolized by bacterial p-aminobenzoate auxotrophs possessing the enzyme p-aminobenzoyl-glutamate hydrolase.
[Synthesis]

P-NITROBENZOYL-L-GLUTAMIC ACID

6758-40-3

N-(p-Aminobenzoyl)glutamic acid

4271-30-1

General procedure for the synthesis of N-(4-aminobenzoyl)-L-glutamic acid from N-p-nitrobenzoylglutamic acid: 27.23 g (0.1 mol) of N-nitrobenzoyl-L-glutamic acid and 118 g of methanol were added to a reaction vessel, and stirred until complete dissolution. Subsequently, 0.59 g of 10% Pd/C catalyst was added and 18.92 g (0.3 mol) of ammonium formate was added slowly. The reaction mixture was stirred at room temperature and kept for 30 minutes. After completion of the reaction, the Pd/C catalyst was recovered by filtration. The filtrate was adjusted to pH=3 with hydrochloric acid in methanol and left to stand for 30 min before filtering the precipitated crystals. The crystals were washed with a small amount of methanol and dried to give 25.75 g of N-(4-aminobenzoyl)-L-glutamic acid, with 99.88% purity by HPLC, 96.58% yield, and 95.64% total yield as nitrobenzoic acid.

[Purification Methods]

Crystallise the acid from H2O. Also purify it by dissolving 2.7g in H2O (130mL), adding aqueous NaOH to pH 5.5 and adding portionwise a solution of 0.5M CuSO4 to complete precipitation of the Cu salt. This salt is filtered off, suspended in H2O and H2S is bubbled through to precipitate CuS, filter, evaporate and recrystallise the residue from H2O. It has max (H2O) at 273nm. [Backer & Houtman Recl Trav Chim Pays-Bas 70 738, 743 1951, Beilstein 14 IV 1153.]
[References]

[1] Patent: CN105439895, 2016, A. Location in patent: Paragraph 0029; 0030
[2] Chirality, 2010, vol. 22, # 2, p. 252 - 257
[3] Journal of the Chemical Society, 1949, p. 1401,1404
[4] Yakugaku Zasshi, 1949, vol. 69, p. 457
[5] Chem.Abstr., 1950, p. 3442
Spectrum DetailBack Directory
[Spectrum Detail]

N-(p-Aminobenzoyl)glutamic acid(4271-30-1)1HNMR
N-(p-Aminobenzoyl)glutamic acid(4271-30-1)IR1
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

4271-30-1(sigmaaldrich)
[TCI AMERICA]

N-(4-Aminobenzoyl)-L-glutamic Acid,>97.0%(T)(4271-30-1)
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