ChemicalBook > CAS DataBase List > 5,8-Dihydroxy-1,4-naphthoquinone

5,8-Dihydroxy-1,4-naphthoquinone

Product Name
5,8-Dihydroxy-1,4-naphthoquinone
CAS No.
475-38-7
Chemical Name
5,8-Dihydroxy-1,4-naphthoquinone
Synonyms
NAPHTHAZARIN;5,8-Dihydroxynaphthoquinone;5,8-Dihydroxynaphthalene-1,4-dione;Naphthazarone;Naphthazarine;NAPHTHAZALINE;Mordant Black 37;Naphthazarin (6CI);5,8-Dihydroxy-1,4-n;5,8-dihydroxy-4-naphthoquinone
CBNumber
CB8194974
Molecular Formula
C10H6O4
Formula Weight
190.15
MOL File
475-38-7.mol
More
Less

5,8-Dihydroxy-1,4-naphthoquinone Property

Melting point:
220-230 °C(lit.)
Boiling point:
285.64°C (rough estimate)
Density 
1.3366 (rough estimate)
refractive index 
1.5280 (estimate)
storage temp. 
Sealed in dry,Room Temperature
form 
powder to crystaline
pka
6.98±0.20(Predicted)
color 
Dark red to Brown
Water Solubility 
Soluble in water (5520 mg/L 25.).
BRN 
880561
CAS DataBase Reference
475-38-7(CAS DataBase Reference)
NIST Chemistry Reference
1,4-Naphthalenedione, 5,8-dihydroxy-(475-38-7)
More
Less

Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
22-24/25-37/39-26
WGK Germany 
3
RTECS 
QL7970000
HS Code 
2914409000
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P271Use only outdoors or in a well-ventilated area.

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

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P405Store locked up.

P501Dispose of contents/container to..…

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
388513
Product name
5,8-Dihydroxy-1,4-naphthoquinone
Purity
technical grade
Packaging
1g
Price
$293
Updated
2024/03/01
TCI Chemical
Product number
D2070
Product name
5,8-Dihydroxy-1,4-naphthoquinone
Purity
>75.0%(HPLC)
Packaging
1g
Price
$401
Updated
2024/03/01
TCI Chemical
Product number
D2070
Product name
5,8-Dihydroxy-1,4-naphthoquinone
Purity
>75.0%(HPLC)
Packaging
5g
Price
$406
Updated
2021/12/16
Alfa Aesar
Product number
A18930
Product name
5,8-Dihydroxy-1,4-naphthoquinone, 97%
Packaging
1g
Price
$98.2
Updated
2021/12/16
Alfa Aesar
Product number
A18930
Product name
5,8-Dihydroxy-1,4-naphthoquinone, 97%
Packaging
5g
Price
$415
Updated
2021/12/16
More
Less

5,8-Dihydroxy-1,4-naphthoquinone Chemical Properties,Usage,Production

Chemical Properties

dark purple to brown-black powder

Definition

ChEBI: A naphthoquinone that is 1,4-naphthoquinone in which the hydrogens at positions 5 and 8 are replaced by hydroxy groups.

Preparation

1,8-Dinitronaphthalene and 1,5-Dinitronaphthalene mixture or both alone and one of sulfur 40% fuming sulfuric ACID reaction, the product (5, 8 – dihydroxy – naphthoquinone) into Sulfurous acid?hydrogen salt.

Properties and Applications

ash red to black. Soluble in water for red light brown, soluble in ethanol for yellow brown, with green fluorescence. In concentrated sulfuric acid to dark yellow green, heating to rouge red, dilution after brown black precipitation. Dye aqueous solution to join sodium hydroxide to red, the air oxidation into blue.

Standard Ironing Fastness Light Fastness Fulling Persperation Fastness Soaping Water
Alkali Acid
ISO 5 6 5 4 5 5 5

Purification Methods

It crystallises in red-brown needles with a green shine from EtOH. It also crystallises from hexane and is further purified by sublimation at 2-10mm. [Huppert et al. J Phys Chem 89 5811 1985.] It is sparingly soluble in H2O but soluble in alkalis. The diacetate forms golden yellow prisms from CHCl3, m 192-193o and the 5,8-dimethoxy derivative has m 157o (155o) (from pet ether) [Bruce & Thompson J Chem Soc 1089 1955, IR: Schmand & Boldt J Am Chem Soc 97 447 1975, NMR: Brockmann & Zeeck Chem Ber 101 4221 1968]. The monothiosemicarbazone has m 168o(dec) from EtOH [Gardner et al. J Am Chem Soc 74 2106 1952]. [Beilstein 8 H 412, 8 III 3600.]

5,8-Dihydroxy-1,4-naphthoquinone Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

5,8-Dihydroxy-1,4-naphthoquinone Suppliers

Henan Lavoisier Chemical Products Co. Ltd
Tel
0371-63682289 18625781376
Fax
18625781376
Email
jacschem@163.com
Country
China
ProdList
5008
Advantage
58
Nanjing Chemlin Chemical Co., Ltd
Tel
025-83697070
Fax
+86-25-83453306
Email
info@chemlin.com.cn
Country
China
ProdList
19172
Advantage
64
https://www.shachemlin.cn/
Tel
15021879576
Email
ming-jiao.wu@chemlin.com.cn
Country
China
ProdList
9959
Advantage
58
Henan Evonik Biotechnology Co. LTD
Tel
16650615803
Email
hnyingchuang@163.com
Country
China
ProdList
3926
Advantage
58
J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
94657
Advantage
76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
021-61259108 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40228
Advantage
62
Alfa Aesar
Tel
400-6106006
Fax
021-67582001/03/05
Email
saleschina@alfa-asia.com
Country
China
ProdList
30123
Advantage
84
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24529
Advantage
81
Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44689
Advantage
61
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696
Email
info@hanhongsci.com
Country
China
ProdList
42958
Advantage
64
Syntechem Co.,Ltd
Tel
Fax
E-Mail Inquiry
Email
info@syntechem.com
Country
China
ProdList
12984
Advantage
57
Hangzhou Yuhao Chemical Technology Co., Ltd
Tel
0571-82693216
Fax
+86-571-82880190
Email
info@yuhaochemical.com
Country
China
ProdList
9387
Advantage
52
Shanghai T&W Pharmaceutical Co., Ltd.
Tel
+86 21 61551611
Fax
+86 21 50676805
Country
China
ProdList
9891
Advantage
58
9ding chemical ( Shanghai) Limited
Tel
4009209199
Fax
86-021-52271987
Email
sales@9dingchem.com
Country
China
ProdList
22514
Advantage
55
Shanghai Aladdin Bio-Chem Technology Co.,LTD
Tel
400-400-6206333 18521732826
Fax
021-50323701
Email
market@aladdin-e.com
Country
China
ProdList
25003
Advantage
65
Hefei NaNo Biological Technology Co., Ltd.
Tel
0551-65629887 18010855303
Fax
0551-65629887
Email
sales@hfnhsw.com
Country
China
ProdList
261
Advantage
58
Sigma-Aldrich
Tel
021-61415566 800-8193336
Email
orderCN@merckgroup.com
Country
China
ProdList
51456
Advantage
80
Tcichem, Inc.
Tel
13918644899
Fax
-
Email
tianchong009@hotmail.com
Country
China
ProdList
1784
Advantage
55
Henan CoreyChem Co., Ltd
Tel
0371-86658258
Fax
0371-60996044
Email
info@coreychem.com
Country
China
ProdList
10453
Advantage
58
Chengdu Dianchun Technology Co., Ltd
Tel
400-1166-196 18502815961
Fax
QQ:800101999
Email
cdhxsj@163.com
Country
China
ProdList
14603
Advantage
60
Amadis Chemical Company Limited
Tel
571-89925085
Fax
0086-571-89925065
Email
sales@amadischem.com
Country
China
ProdList
131957
Advantage
58
Beijing Jin Ming Biotechnology Co., Ltd.
Tel
010-60605840 18892239720
Fax
010-60605840
Email
psaitong@jm-bio.com
Country
China
ProdList
12306
Advantage
58
Wuhan EEChem Technologies Co., Ltd
Tel
0711-3617768 13308685235
Fax
0711-3616558
Email
lihongcai4360@sina.com
Country
China
ProdList
1378
Advantage
55
9ding chemical ( Shanghai) Limited
Tel
021-021-52271985 17721149837
Fax
+86 (21) 52271987
Email
sales@9dingchem.com
Country
China
ProdList
19800
Advantage
60
Jiaxing Deyi Chemical Co., Ltd.
Tel
0573-86-0573-85866609 13325730825
Fax
0573-85866609
Email
945717149@qq.com
Country
China
ProdList
8025
Advantage
58
Shanghai Standard Technology Co.,Ltd.
Tel
021-021-57127007-6622-6622 15618937986
Fax
+86 (21) 5132-0077
Email
zhaok@nature-standard.com
Country
China
ProdList
3016
Advantage
58
Aikon International Limited
Tel
025-66113011 18112977050
Fax
(5)02557626880
Email
cb6@aikonchem.com
Country
China
ProdList
15494
Advantage
58
Rhawn Reagent
Tel
400-400-1332688 18019345275
Fax
400-133-2688
Email
amy@rhawn.cn
Country
China
ProdList
15497
Advantage
58
Zhengzhou Ruke Biological Co., Ltd.
Tel
15981811963
Fax
QQ:1410472904
Email
1410472904@qq.com
Country
China
ProdList
5825
Advantage
58
Tianjin heowns Biochemical Technology Co., Ltd.
Tel
400-6387771-6038 18902104717
Email
sales@heowns.com
Country
China
ProdList
21085
Advantage
60
Shanghai Jizhi Biochemical Technology Co. Ltd.
Tel
4009004166/18616739031 18616739031
Email
3007523370@qq.com
Country
China
ProdList
52693
Advantage
58
Shanghai Hongye Biotechnology Co. Ltd
Tel
400-9205774
Email
sales@glpbio.cn
Country
China
ProdList
6777
Advantage
58
Shanghai Meiquan Chemical Technology Co., Ltd.
Tel
021-18130556 18130556558
Email
zkq1984@163.com
Country
China
ProdList
382
Advantage
58
Nanjing Asfam Pharmaceutical Technology Co., Ltd.
Tel
025-58867862 18751812725
Fax
02558867862
Email
sales@ace-pharm.com
Country
China
ProdList
1994
Advantage
58
Henan Alfa Chemical Co., Ltd
Tel
+86-18339805032; +8618339805032
Email
alfa4@alfachem.cn
Country
China
ProdList
13227
Advantage
58
Dayang Chem (Hangzhou) Co.,Ltd.
Tel
571-88938639 +8617705817739
Fax
+86-571-88938652,+86-571- 88492614
Email
info@dycnchem.com
Country
China
ProdList
52849
Advantage
58
SIMAGCHEM CORP
Tel
+86-13806087780
Email
sale@simagchem.com
Country
China
ProdList
17365
Advantage
58
Henan Weituxi Chemical Technology Co., Ltd.
Tel
0371-63284658 18135795563
Fax
QQ:2885349392
Email
2885349392@qq.com
Country
China
ProdList
10058
Advantage
58
Zhengzhou Edward Biology Co.,Ltd
Tel
0371-63682289 15538176268
Fax
QQ:1875164801
Email
jacschem@163.com
Country
China
ProdList
9998
Advantage
58
career henan chemical co
Tel
+86-0371-86658258 +8613203830695
Fax
0086-371-86658258
Email
factory@coreychem.com
Country
China
ProdList
29811
Advantage
58
Shaanxi Dideu Medichem Co. Ltd
Tel
18192627656
Fax
+86-29-88380327
Email
1012@dideu.com
Country
China
ProdList
3002
Advantage
58
Beijing Aomi Jiade Pharmaceutical Technology Co., Ltd
Tel
+86-13522808617 +86-13522808617
Email
omichem@126.com
Country
China
ProdList
9211
Advantage
58
CHG Opto-Electronic Corporation Limited
Tel
2537653158 16621191650
Fax
QQ 2537653158
Email
2537653158@qq.com
Country
China
ProdList
6884
Advantage
58
cjbscvictory
Tel
13348960310 13348960310
Email
3003867561@qq.com
Country
China
ProdList
10002
Advantage
58
Beijing Jin Ming Biotechnology Co., Ltd.
Tel
010-60605840 15801484223;
Email
psaitong@jm-bio.com
Country
China
ProdList
29774
Advantage
58
Hebei Zhenjia new material Co., LTD
Tel
0319-5925599 13315915972
Email
13313090628@163.com
Country
China
ProdList
2918
Advantage
58
Bide Pharmatech Ltd.
Tel
400-1647117 13681763483
Email
product02@bidepharm.com
Country
China
ProdList
62163
Advantage
58
Suzhou Victorypharm Co.,Ltd.
Tel
512-68242903 13916956214
Email
sales@victory-pharm.com
Country
China
ProdList
1394
Advantage
58
Shaanxi DIDU pharmaceutical and Chemical Co., Ltd
Tel
17691182729 18161915376
Email
1046@dideu.com
Country
China
ProdList
10007
Advantage
58
Shanghai Huici Pharmaceutical Technology Co., LTD
Tel
19372841038 19372841038
Email
lixing@pharmahuici.com
Country
China
ProdList
248
Advantage
58
More
Less

View Lastest Price from 5,8-Dihydroxy-1,4-naphthoquinone manufacturers

Zibo Hangyu Biotechnology Development Co., Ltd
Product
5,8-Dihydroxy-1,4-naphthoquinone 475-38-7
Price
US $150.00-430.00/g
Min. Order
1g
Purity
99%
Supply Ability
30
Release date
2024-07-10
Shaanxi Dideu Medichem Co. Ltd
Product
5,8-Dihydroxy-1,4-naphthoquinone 475-38-7
Price
US $1.00-22.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
100000KG
Release date
2024-08-02
Henan Aochuang Chemical Co.,Ltd.
Product
5,8-Dihydroxy-1,4-naphthoquinone 475-38-7
Price
US $0.00-0.00/KG
Min. Order
1KG
Purity
98%
Supply Ability
1ton
Release date
2022-10-09

475-38-7, 5,8-Dihydroxy-1,4-naphthoquinoneRelated Search:


  • ,8-Dihydroxy-[1,4]naphthoquinone
  • ,8-Dihydroxy-1,4-naphthalenedione
  • 1,4-Naphthoquinone, 5,8-dihydroxy-
  • 2,3-Dihydro-1,4,5,8-naphthalenetetrone
  • 5,8-dihydroxy-4-naphthalenedione
  • 5,8-dihydroxy-4-naphthoquinone
  • 5,8-Dihydroxynaphthoquinone
  • Naphthazarine
  • Naphthazarone
  • 5,8-DIHYDROXY-1,4-NAPHTHALENEDIONE
  • 5,8-DIHYDROXY-1,4-NAPHTHOQUINONE
  • DIHYDROXY-1,4-NAPHTHOQUINONE,5,8-
  • NAPHTHAZARIN
  • 5,8-HYDROXY-1,4-NAPHTHOQUINONE
  • NAPHTHAZALINE
  • 5,8-DIHYDROXY-1,4-NAPHTHOQUINONE, TECH.
  • 5,8-Dihydroxy-1,4-naphthoquinone,tech.90%
  • 5,8-Dihydroxy-1,4-n
  • 5,8-Dihydroxynaphthalene-1,4-dione
  • 5,8-Dihydroxy-1,4-naphthoquinone,98%
  • 5,8-Dihydroxy-1,4-naphthalenedione Naphthazarin
  • 5,8-dihydroxy-2,3-dihydronaphthalene-1,4-dione
  • 5,8-Dihydroxy-1,4-naphthoquinone&gt
  • 1,4-Naphthalenedione, 5,8-dihydroxy-
  • C.I.Mordant Black 37:C.I.57010
  • Mordant Black 37
  • Naphthazarin (6CI)
  • Naturally,Apoptosis,Naphthazarin,stress,microtubules,mitochondrial,AIF,Inhibitor,p21,lysosomal,inhibit,oxidative,p53-dependent,anti-tumor
  • 475-38-7
  • HO2C10H4O2
  • Carbonyl Compounds
  • C10
  • Building Blocks
  • Organic Building Blocks
  • Ketones
  • API intermediates