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FMOC-4-AMINOBENZOIC ACID

CAS No.
185116-43-2
Chemical Name:
FMOC-4-AMINOBENZOIC ACID
Synonyms
FMOC-PABA-OH;FMOC-P-ABZ-OH;FMOC-4-ABZ-OH;RARECHEM EM WB 0013;FMOC-4-AMINOBENZOIC ACID;Fmoc-PABA-OH Novabiochem;4-(FMOC-AMINO)BENZOIC ACID;N-FMOC-4-AMINOBENZOIC ACID;Fmoc-4-aminobenzoic acid98+%;4-(FMOC-AMINO)BENZOIC ACID 96+%
CBNumber:
CB9437320
Molecular Formula:
C22H17NO4
Molecular Weight:
359.37
MDL Number:
MFCD00144888
MOL File:
185116-43-2.mol
MSDS File:
SDS
Last updated:2025-07-24 18:13:46

FMOC-4-AMINOBENZOIC ACID Properties

Melting point ~277 °C (dec.)
Boiling point 544.9±33.0 °C(Predicted)
Density 1.352±0.06 g/cm3(Predicted)
storage temp. 2-8°C
pka 4.29±0.10(Predicted)
form powder
Appearance White to off-white Solid
BRN 7722986
CAS DataBase Reference 185116-43-2(CAS DataBase Reference)
UNSPSC Code 12352209
NACRES NA.26

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H335-H319-H315
Precautionary statements  P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362
Safety Statements  22-24/25
WGK Germany  3
10
HS Code  2924 29 70
HazardClass  IRRITANT
NFPA 704
0
0 0

FMOC-4-AMINOBENZOIC ACID price More Price(31)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 8.52219 Fmoc-PABA-OH Novabiochem? 185116-43-2 1g $28.6 2025-07-31 Buy
Sigma-Aldrich 8.52219 Fmoc-PABA-OH Novabiochem? 185116-43-2 5G $71.8 2025-07-31 Buy
Sigma-Aldrich 8.52219 Fmoc-PABA-OH Novabiochem? 185116-43-2 25g $295 2025-07-31 Buy
Sigma-Aldrich 47307 Fmoc-4-Abz-OH ≥96.0% (TLC) 185116-43-2 1g $83.1 2025-07-31 Buy
TRC F603565 Fmoc-4-aminobenzoicacid 185116-43-2 500mg $65 2021-12-16 Buy
Product number Packaging Price Buy
8.52219 1g $28.6 Buy
8.52219 5G $71.8 Buy
8.52219 25g $295 Buy
47307 1g $83.1 Buy
F603565 500mg $65 Buy

FMOC-4-AMINOBENZOIC ACID Chemical Properties,Uses,Production

Chemical Properties

White powder

Uses

Fmoc-4-aminobenzoic acid is used in the improved rapid synthesis of oligo(benzamide) block copolymers.

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

Synthesis

9-Fluorenylmethyl chloroformate

28920-43-6

4-Aminobenzoic acid

150-13-0

FMOC-4-AMINOBENZOIC ACID

185116-43-2

Under an inert atmosphere, p-aminobenzoic acid (10 g, 73 mmol) was dissolved in anhydrous N-methylpyrrolidone (NMP, 50 mL). Subsequently, a solution of anhydrous NMP (50 mL) of 9-fluorenylmethyl chloroformate (Fmoc-Cl, 18.9 g, 73 mmol) was slowly added dropwise. The reaction mixture was stirred at room temperature for 24 hours. Upon completion of the reaction, the mixture was slowly poured into 400 mL of water to precipitate the product. The colorless precipitate was collected by filtration and washed with plenty of water. Finally, the product was dried under vacuum at 120 °C to afford N-Fmoc-p-aminobenzoic acid (24.8 g, 94% yield). The melting point of the product was 215 °C (decomposition). Nuclear magnetic resonance hydrogen spectrum (1H-NMR, 300 MHz, DMSO-d6): δ 4.33 (t, J = 6.25 Hz, 1H), 4.54 (d, J = 6.25 Hz, 2H), 7.33-7.45 (m, 4H), 7.57 (d, J = 7.35 Hz, 2H), 7.76 (d, J = 7.35 Hz, 2H), and 7.89 (m, 4H), 10.08 (s, 1H), 12.69 (s, 1H). NMR carbon spectrum (13C-NMR and DEPT, 300 MHz, DMSO-d6): δ 46.61 (CH2), 65.83 (CH), 117.5 (CH), 120.22 (CH), 124.48 (C), 125.14 (CH), 127.17 (CH), 127.74 (CH), 130.48 ( CH), 140.86 (C), 143.31 (C), 143.74 (C), 153.31 (C), 167.03 (C). Infrared spectra (IR, ν, cm-1): 3344, 2970, 2887, 2660, 2544, 1709, 1673, 1610, 1592, 1526, 1511, 1411, 1311, 1282, 1221, 1052, 850, 736. reversed-phase high performance liquid chromatography (RP-HPLC) retention time: 26.6 Minutes. Mass spectrometry (FD-MS): m/z (%) = 359.1 (100), 360.1 (17.4); calculated value [C22H17NO4] = 359.1.

References

[1] Tetrahedron Letters, 2013, vol. 54, # 8, p. 753 - 756
[2] Chemical Communications, 2013, vol. 49, # 40, p. 4555 - 4557
[3] Journal of Chemical Research, Miniprint, 1998, # 10, p. 2736 - 2753
[4] Chemical Communications, 2014, vol. 50, # 14, p. 1691 - 1693

28920-43-6
150-13-0
185116-43-2
Synthesis of FMOC-4-AMINOBENZOIC ACID from 9-Fluorenylmethyl chloroformate and 4-Aminobenzoic acid

FMOC-4-AMINOBENZOIC ACID Preparation Products And Raw materials

FMOC-4-AMINOBENZOIC ACID Suppliers

Global( 134)Suppliers
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GenicBio Limited
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Dayang Chem (Hangzhou) Co.,Ltd.
+86-0571-88938639 +8617705817739 info@dycnchem.com China 52846 58

FMOC-4-AMINOBENZOIC ACID Spectrum

FMOC-PABA-OH FMOC-P-ABZ-OH FMOC-4-AMINOBENZOIC ACID FMOC-4-ABZ-OH 4-(FMOC-AMINO)BENZOIC ACID 4-(9-FLUORENYLMETHYLOXYCARBONYL)AMINO-BENZOIC ACID N-ALPHA-9-FLUORENYLMETHOXYCARBONYL-4-AMINOBENZOIC ACID N-ALPHA-9-FLUORENYLMETHOXYCARBONYL-P-AMINOBENZOIC ACID N-ALPHA-FMOC-P-AMINOBENZOIC ACID N-FMOC-4-AMINOBENZOIC ACID RARECHEM EM WB 0013 Benzoic acid, 4-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]- (9CI) 4-(FMOC-AMINO)BENZOIC ACID 96+% FMoc-4-Abz-OH(FMoc-4-aMinobenzoic Acid) Fmoc-4-aminobenzoic acid98+% Fmoc-PABA-OH Novabiochem (9H-Fluoren-9-yl)MethOxy]Carbonyl 4-Abz-OH 4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)benzoic acid 4-amino-2-[9H-fluoren-9-ylmethoxy(oxo)methyl]benzoic acid Benzoic acid, 4-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]- 4-(9H-fluoren-9-ylmethoxycarbonylamino)benzoicaci FMOC-4-AMINOBENZOIC ACID USP/EP/BP 185116-43-2 Aromatic Amino Acids Unnatural Amino Acid Derivatives Peptide Synthesis Specialty Synthesis Unusual Amino Acids Amino Acids FMOC