6-HYDROXY-2-NAPHTHYL DISULFIDE

6-HYDROXY-2-NAPHTHYL DISULFIDE Structure
CAS No.
6088-51-3
Chemical Name:
6-HYDROXY-2-NAPHTHYL DISULFIDE
Synonyms
DDD;DDD0;PIR 3.5;6,6'DDD (Analytical);AKOS BBS-00001974;TIMTEC-BB SBB005947;6′-Dithiodi(2-naphthol);6,6'-Dithiodi-2-naphthtol;6,6'-DITHIODI(2-NAPHTHOL)
CBNumber:
CB8198578
Molecular Formula:
C20H14O2S2
Molecular Weight:
350.45
MOL File:
6088-51-3.mol
MSDS File:
SDS
Modify Date:
2023/6/8 17:06:38

6-HYDROXY-2-NAPHTHYL DISULFIDE Properties

Melting point 226 °C
Boiling point 597.5±25.0 °C(Predicted)
Density 1.46±0.1 g/cm3(Predicted)
storage temp. −20°C
solubility <26.28mg/ml in DMSO
form powder to crystal
pka 8.93±0.40(Predicted)
color White to Brown
Merck 14,2840
CAS DataBase Reference 6088-51-3(CAS DataBase Reference)
EPA Substance Registry System 2-Naphthalenol, 6,6'-dithiobis- (6088-51-3)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319
Precautionary statements  P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
WGK Germany  3
HS Code  2908990090
NFPA 704
0
1 0

6-HYDROXY-2-NAPHTHYL DISULFIDE price More Price(1)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemicals (India) D0244 Bis(6-hydroxy-2-naphthyl) Disulfide 6088-51-3 1G ₹6700 2022-05-26 Buy
Product number Packaging Price Buy
D0244 1G ₹6700 Buy

6-HYDROXY-2-NAPHTHYL DISULFIDE Chemical Properties,Uses,Production

Description

DDD, 1,1-dichloro-2,2-bis-(4-chlorophenyl) ethane, also known as TDE, is a metabolite of DDT, which found use in agriculture. As with DDT, the p,p -isomer is insecticidal and the o,p -isomer is an impurity.

Uses

For determination of protein-bound sulfhydryl groups.

Purification Methods

It crystallises as leaflets from AcOH and is slightly soluble in EtOH, and AcOH, but is soluble in *C6H6 and in alkalis to give a yellow solution. [Zincke & Dereser Chem Ber 51 352 1918.] The acetoxy derivative has m 198-200o (from AcOH or dioxane/MeOH), and the diacetyl derivative has m 167-168o (from AcOH). A small amount of impure disulfide can be purified by dissolving it in a small volume of Me2CO and adding a large volume of toluene, filter rapidly and concentrate to one-third of its volume. The hot toluene solution is filtered rapidly from any tarry residue, and crystals separate on cooling. Recrystallisation from hot acetic acid gives crystals with m 220-223o [Barrett & Seligman Science 116 323 1952]. [Beilstein 6 I 481.]

6-HYDROXY-2-NAPHTHYL DISULFIDE Preparation Products And Raw materials

Raw materials

Preparation Products

6-HYDROXY-2-NAPHTHYL DISULFIDE Suppliers

Global( 92)Suppliers
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A.J Chemicals 91-9810153283 New Delhi, India 6124 58 Inquiry
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6,6'-Dithiodi-2-naphthtol PIR 3.5 DDD (Analytical) DDD 6,6'-Dihydroxy-2,2'-dinaphthyl Disulfide 6-Hydroxy-2-naphthyl Disulfide 2-Naphthalenol,6,6'-dithiobis- 6,6&apos Bis(2-hydroxy-6-naphthyl) disulfide TIMTEC-BB SBB005947 6,6’-dithiobis-2-naphthaleno BIS(6-HYDROXY-2-NAPHTHYL) DISULFIDE DDD 2,2'-DIHYDROXY-6,6'-DINAPHTHYL DISULFIDE 2,2'-DIHYDROXY-6,6'-DINAPHTHYLDISULPHIDE 6,6'-DITHIODI(2-NAPHTHOL) 6,6'-DIHYDROXY-2,2'-DINAPHTHYL DISULFIDE 6-HYDROXY-2-NAPHTHYL DISULFIDE AKOS BBS-00001974 6-HYDROXY-2-NAPHTHYL DISULFIDE 98% 6-HYDROXY-2-NAPHTHYLDISULPHIDE 6-HYDROXY-2-NAPHTHYL DISULFIDE 98+% 6,6μ-Dihydroxy-2,2μ-dinaphthyl disulfide, 6-Hydroxy-2-naphthyl disulfide, Bis(6-hydroxy-2-naphthyl) disulfide 2,2μ-Dihydroxy-6,6μ-dinaphthyl disulfide, 6,6μ-Dihydroxy-2,2μ-dinaphthyl disulfide, 6,6μ-Dithiodi(2-naphthol), 6,6μ-Dithiodi-2-naphthol, Bis(2-hydroxy-6-naphthyl) disulfide, Bis(6-hydroxy-2-naphthyl) disulfide, DDD [6,6'-Dithiodinaphthalene]-2,2'-diol 6,6'-Dithiobis(2-naphthol) Bis(6-hydroxy-2-naphtyl) persulfide DDD0 6′-Dithiodi(2-naphthol) Bis(6-hydroxy-2-naphthyl) Disulfide > 6,6'-Disulfanediylbis(naphthalen-2-ol) 6-[(6-hydroxy-2-naphthalenyl)disulfanyl]-2-naphthalenol 6088-51-3 HOC10H6S2 C20H14O2S2 BioChemical Biochemicals and Reagents Sulfur Compounds (for Synthesis) Detection Fluorescent Probes, Labels, Particles and Stains Sulfur Compounds (for Synthesis) Synthetic Organic Chemistry