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Urocanic acid

CAS No.
104-98-3
Chemical Name:
Urocanic acid
Synonyms
4-IMIDAZOLEACRYLIC ACID;(E)-3-(1H-imidazol-5-yl)acrylic acid;3-(1H-IMIDAZOL-4-YL)ACRYLIC ACID;SKL080;UROCANIC ACID;Urocanic caid;Urocalic acid;urocanoic acid;UROCANINIC ACID;Urocanic acid,99%
CBNumber:
CB8750635
Molecular Formula:
C6H6N2O2
Molecular Weight:
138.12
MDL Number:
MFCD00005203
MOL File:
104-98-3.mol
MSDS File:
SDS
Last updated:2023-11-13 19:05:53

Urocanic acid Properties

Melting point 226-228 °C(lit.)
Boiling point 253.51°C (rough estimate)
Density 1.3471 (rough estimate)
refractive index 1.5100 (estimate)
storage temp. Keep in dark place,Sealed in dry,2-8°C
solubility 1.5g/l
pka 2.94±0.10(Predicted)
form Powder
color White to beige
Water Solubility SLIGHTLY SOLUBLE
BRN 81405
InChI InChI=1S/C6H6N2O2/c9-6(10)2-1-5-3-7-4-8-5/h1-4H,(H,7,8)(H,9,10)
InChIKey LOIYMIARKYCTBW-UHFFFAOYSA-N
SMILES C(O)(=O)C=CC1NC=NC=1
CAS DataBase Reference 104-98-3(CAS DataBase Reference)
EWG's Food Scores 1-3
FDA UNII G8D26XJJ3B
EPA Substance Registry System 2-Propenoic acid, 3-(1H-imidazol-4-yl)- (104-98-3)

SAFETY

Risk and Safety Statements

Safety Statements  22-24/25
WGK Germany  3
RTECS  NI3425200
HazardClass  IRRITANT
HS Code  29332990

Urocanic acid price More Price(17)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 859796 4-Imidazoleacrylic acid 99% 104-98-3 5g $54.3 2024-03-01 Buy
Sigma-Aldrich 859796 4-Imidazoleacrylic acid 99% 104-98-3 25g $258 2024-03-01 Buy
Sigma-Aldrich 859796 4-Imidazoleacrylic acid 99% 104-98-3 100g $813 2024-03-01 Buy
TRC U847063 UrocanicAcid 104-98-3 250mg $50 2021-12-16 Buy
Biosynth Carbosynth FU29984 Urocanic acid 104-98-3 5G $50 2021-12-16 Buy
Product number Packaging Price Buy
859796 5g $54.3 Buy
859796 25g $258 Buy
859796 100g $813 Buy
U847063 250mg $50 Buy
FU29984 5G $50 Buy

Urocanic acid Chemical Properties,Uses,Production

Chemical Properties

White to beige fine powder. 

Uses

Urocanic Acid is a biomarker in the fecal metabolic profiling of breast cancer patients.

Definition

ChEBI: Urocanic acid is an alpha,beta-unsaturated monocarboxylic acid that is prop-2-enoic acid substituted by a 1H-imidazol-4-yl group at position 3. It is a metabolite of hidtidine. It has a role as a chromophore and a human metabolite. It is an alpha,beta-unsaturated monocarboxylic acid and a member of imidazoles. It is a conjugate acid of a urocanate.

Biological Functions

Urocanic acid, produced in the upper layers of mammalian skin, is a major absorber of ultraviolet radiation (UVR). Urocanic acid (UCA) is formed in the upper layers of the epidermis where filaggrin, a histidine-rich filamentous protein produced after caspase-14 cleavage of profilaggrin, is broken down by proteinases into component amino acids.

General Description

4-Imidazoleacrylic acid also known as urocanic acid is a natural metabolite derived from histidine. It is majorly used as a UV chromophore with a strong absorption spectrum in the UV-B region in the range of 300-280 nm.

Synthesis

A method of producing trans-urocanic acid, which involves treating D-glucose with aqueous ammonia and formalin in molar ratio D-glucose: aqueous ammonia: formalin equal to 1:24:2.7, in water in the presence of basic copper carbonate at temperature 85-90°C for 3 hours to form (1S,2S,3S)-1-(1H-imidazol-4-yl)-butane-1,2,3,4-tetrazole, which is extracted in form of a hydrochloride. Through periodate splitting in water, the obtained (1S,2S,3S)-1-(1H-imidazol-4-yl)-butane-1,2,3,4-tetrazole is converted at room temperature to 1H-imidazole-4-carbaldehyde, condensation of which, in acetic anhydride in the presence of anhydrous potassium acetate at temperature 120°C for 2 hours, leads to formation of trans-urocanic acid with subsequent extraction thereof from the reaction mass.

Purification Methods

Crystallise the acid from water and dry it at 100o. The trans-isomer [3465-72-3] has m 225o (229-230o, 230-231o or 231o(dec, from H2O) and pK1 3.5 and pK2 5.6, and the picrate has m 225o(dec, from H2O). The cis-isomer [7699-35-6] has m 175-176o (178-179o or 180-184o dec, from H2O) and pK1 3.0 and pK2 6.7, and the picrate has m 204o (from H2O). [Beilstein 25 H 124, 25 I 536, 25 II 121, 25 III/IV 786.]

71-00-1
104-98-3
Synthesis of Urocanic acid from L-Histidine
Global( 170)Suppliers
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View Lastest Price from Urocanic acid manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Urocanic acid pictures 2023-11-13 Urocanic acid
104-98-3
US $0.00 / KG 1KG 99% 50000KG/month Hebei Mojin Biotechnology Co., Ltd
Urocanic acid pictures 2023-09-06 Urocanic acid
104-98-3
US $0.00-0.00 / KG 50KG 99% 500000kg Hebei Guanlang Biotechnology Co., Ltd.
  • Urocanic acid pictures
  • Urocanic acid
    104-98-3
  • US $0.00 / KG
  • 99%
  • Hebei Mojin Biotechnology Co., Ltd
  • Urocanic acid pictures
  • Urocanic acid
    104-98-3
  • US $0.00-0.00 / KG
  • 99%
  • Hebei Guanlang Biotechnology Co., Ltd.
(E)-3-(3H-imidazol-4-yl)acrylic acid 3-(1H-imidazol-4-yl)prop-2-enoic acid 3-(3H-imidazol-4-yl)acrylic acid 1H-Imidazole-4-acrylic acid 1H-Imidazole-5-acrylic acid Urocanic acid,99% 4-Imidazoleacrylic acid,3-(4-Imidazolyl)acrylic acid, Urocanic acid (E)-3-(1H-Imidazol-5-yl)-2-propenoic acid Urocanic acid, 99% 25GR 2-Propenoic acid,3-(1H-iMidazol-5-yl)- 4-IMidazoleacrylic acid 99% trans-Urocanic Acid , 98.0%(LC&T 3-(4-IMIDAZOLY)ACRYLIC ACID 3,4-IMIDAZOLYLACRYLIC ACID (E)-3-(1H-IMIDAZOL-4-YL)-ACRYLIC ACID IMIDAZOLE-4-ACRYLIC ACID B 4(5)-GLYOXALINYLACRYLIC ACID RARECHEM AL BK 0762 TIMTEC-BB SBB006702 UROCANIC ACID UROCANINIC ACID 2-Propenoic acid, 3-(1H-imidazol-4-yl)- 3-(3H-imidazol-4-yl)prop-2-enoic acid UROCANIC ACID 99% Urocanic caid urocanoic acid 3-(4-Imidazolyl)acrylic acid, Urocanic acid 4-IMIDAZOLEacrylic acid: 3-(4-imidazolyl)acrylic acid 3-(1H-Imidazol-4-yl) Imidazole-4-acrylic acid for synthesis 3-(1h-imidazol-4-yl)-2-propenoicaci 3-(1h-imidazol-4-yl)-2-propenoicacid 3-imidazol-4-ylacrylic 3-imidazol-4-ylacrylicacid 5-imidazoleacrylicacid imidazoleacrylicacid 1H-Imidazole-4-acrylic acid (Urocanic acid) Urocalic acid Histidine metabolism 3-imi dazo1-4-ylaery1i c acid 4-Imidazolylacrylic acid 4-lmidazdeacrylic acid SKL080 (Z)-3-(1H-imidazol-5-yl)prop-2-enoic acid 3-(1H-IMIDAZOL-4-YL)ACRYLIC ACID (E)-3-(1H-imidazol-5-yl)acrylic acid 4-IMIDAZOLEACRYLIC ACID 3-(1H-imidazol-5-yl)acrylic acid Urinary acid Reference Standards 104-98-3 104-93-3 104-98-03 C6H6N2O22H2O CARBOXYLIC ACID Heterocyclic Building Blocks Imidazoles Building Blocks Imidazoles, Pyrroles, Pyrazoles, Pyrrolidines