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XANTHURENIC ACID

Product Name
XANTHURENIC ACID
CAS No.
59-00-7
Chemical Name
XANTHURENIC ACID
Synonyms
NSC 401570;JACS-59-00-7;xanthurenate;XANTHURIC ACID;XANTHURENIC ACID;XENTHURENIC ACID;TIMTEC-BB SBB003498;XANTHURENIC ACID(RG);Xanthurenic acid 96%;8-hydroxykynurenicacid
CBNumber
CB7180163
Molecular Formula
C10H7NO4
Formula Weight
205.17
MOL File
59-00-7.mol
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XANTHURENIC ACID Property

Melting point:
297-298 °C (dec.)(lit.)
Boiling point:
343.83°C (rough estimate)
Density 
1.3849 (rough estimate)
refractive index 
1.5600 (estimate)
storage temp. 
Sealed in dry,2-8°C
solubility 
DMSO (Slightly, Heated), Water (Slightly, Heated)
pka
1.20±0.30(Predicted)
form 
Powder
color 
Ochre
Merck 
14,10068
BRN 
185954
CAS DataBase Reference
59-00-7(CAS DataBase Reference)
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36-37/39
WGK Germany 
3
RTECS 
UZ9275000
HS Code 
29334900
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
D120804
Product name
Xanthurenic acid
Purity
96%
Packaging
1g
Price
$64.7
Updated
2023/06/20
Sigma-Aldrich
Product number
D120804
Product name
Xanthurenic acid
Purity
96%
Packaging
5g
Price
$206
Updated
2023/06/20
TCI Chemical
Product number
X0054
Product name
Xanthurenic Acid
Purity
>96.0%(HPLC)(T)
Packaging
1g
Price
$132
Updated
2024/03/01
Cayman Chemical
Product number
19191
Product name
Xanthurenic Acid
Purity
≥95%
Packaging
1g
Price
$50
Updated
2024/03/01
Cayman Chemical
Product number
19191
Product name
Xanthurenic Acid
Purity
≥95%
Packaging
5g
Price
$230
Updated
2024/03/01
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XANTHURENIC ACID Chemical Properties,Usage,Production

Chemical Properties

ochre powder

Uses

caspase activator, guanylyl cyclase stimulant

Uses

Xanthurenic acid can be used as a substrate for the synthesis of:

  • Silica-gel functionalized xanthurenic acid (4, 8-dihydroxyquinoline-2-carboxylic acid) as an adsorbent for metal ions.
  • N, N′-bis-((8-hydroxy-7-quinolinyl)methyl)-1,10-diaza-18-crown-6 ethers as fluorescent sensors of magnesium in living cells via one-pot Mannich reaction.
  • Poly-xanthurenic acid (poly-Xa) for biosensing applications.

Uses

Excreted by pyridoxine-deficient animals after the ingestion of tryptophan.

Definition

ChEBI: A quinolinemonocarboxylic acid that is quinoline-2-carboxylic acid substituted by hydroxy groups at C-4 and C-8.

storage

Room temperature

Purification Methods

It is precipitated by the addition of 2N formic acid to its solution in hot 2M ammonia (charcoal). The solid is filtered off, dried in a vacuum at ~80o in the dark. UV (H2O) has nm ( M-1cm-1): 243 (30,000) and 342 (6,500). The methyl ester has m 262o (from MeOH). It forms Cu2+, Zn2+, Fe2+ and Fe3+ salts. [Beilstein 22 III/IV 2513.]

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XANTHURENIC ACID Suppliers

J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006608290; 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40241
Advantage
62
3B Pharmachem (Wuhan) International Co.,Ltd.
Tel
821-50328103-801 18930552037
Fax
86-21-50328109
Email
3bsc@sina.com
Country
China
ProdList
15848
Advantage
69
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24539
Advantage
81
Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44751
Advantage
61
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696;
Email
info@hanhongsci.com
Country
China
ProdList
42982
Advantage
64
Chemsky(shanghai)International Co.,Ltd.
Tel
021-50135380
Email
shchemsky@sina.com
Country
China
ProdList
32344
Advantage
50
Syntechem Co.,Ltd
Tel
Fax
E-Mail Inquiry
Email
info@syntechem.com
Country
China
ProdList
12990
Advantage
57
BEST-REAGENT
Tel
400-1166-196 18981987031
Fax
028-84555506 800101999
Email
cdhxsj@163.com
Country
China
ProdList
11726
Advantage
57
China Langchem Inc.
Tel
0086-21-58956006
Fax
0086-21-58956100
Country
China
ProdList
7815
Advantage
57
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View Lastest Price from XANTHURENIC ACID manufacturers

Hebei Zhanyao Biotechnology Co. Ltd
Product
XANTHURENIC ACID 59-00-7
Price
US $10.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
20 tons
Release date
2021-10-14
Shaanxi Dideu Medichem Co. Ltd
Product
XANTHURENIC ACID 59-00-7
Price
US $0.10/KG
Min. Order
1KG
Purity
99.0%
Supply Ability
1000 tons
Release date
2020-04-28
Career Henan Chemical Co
Product
xanthurenic acid 59-00-7
Price
US $3.00/KG
Min. Order
1KG
Purity
98%
Supply Ability
200KG
Release date
2020-01-09

59-00-7, XANTHURENIC ACIDRelated Search:


  • XANTHURENIC ACID
  • XANTHURIC ACID
  • XENTHURENIC ACID
  • TIMTEC-BB SBB003498
  • 4,8-DIHYDROXYQUINOLINE-2
  • 4,8-DIHYDROXYQUINOLINE-2-CARBOXYLIC ACID
  • 4,8-dihydroxy-2-quinolinecarboxylicaci
  • 4,8-dihydroxy-quinaldicaci
  • 4,8-dihydroxyquinaldinicacid
  • 8-hydroxykynurenicacid
  • 4,8-DIHYDROXY-2-QUINOLINECARBOXYLIC ACID
  • 4,8-DIHYDROXYQUINALDIC ACID
  • 2-Quinolinecarboxylic acid, 4,8-dihydroxy-
  • XANTHURENIC ACID(RG)
  • XANTHURENIC ACID extrapure
  • 4,8-Dihydroxyquinaldic acid, 4,8-Dihydroxyquinoline-2-carboxylic acid
  • 4,8-Dihydroxyquinoline-2-carboxylic acid,96%
  • 4,8-Dihydroxyquinoline-2-carboxylic acid, 96% 1GR
  • 4,8-DIHYDROXYQUINOLINE-2-CARBOXYLIC ACID 96%
  • NSC 401570
  • Xanthurenic acid 96%
  • 4,8-Dihydroxy-2-quinolinecarboxylic acid for synthesis
  • JACS-59-00-7
  • xanthurenate
  • XANTHURENIC ACID ISO 9001:2015 REACH
  • 59-00-7
  • C10H7O4N
  • CARBOXYLIC ACID
  • Hydroxyquinolines
  • Quinolines
  • Heterocyclic Building Blocks
  • Building Blocks
  • Hydroxyquinolines
  • Quinolines
  • Building Blocks
  • C8 to C10
  • Chemical Synthesis
  • Heterocyclic Building Blocks
  • Inhibitors
  • Amines
  • Aromatics
  • Heterocycles
  • Quinolines, Quinazolines and derivatives