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Naphtalene-1,3,6-trisulfonic Acid

Product Name
Naphtalene-1,3,6-trisulfonic Acid
CAS No.
86-66-8
Chemical Name
Naphtalene-1,3,6-trisulfonic Acid
Synonyms
2,5,7-Naphthalenetrisulfonic acid;naphthalene-1,3,6-trisulphonic acid
CBNumber
CB8875761
Molecular Formula
C10H8O9S3
Formula Weight
368.36
MOL File
86-66-8.mol
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Naphtalene-1,3,6-trisulfonic Acid Property

Density 
1.919±0.06 g/cm3(Predicted)
pka
-0.76±0.40(Predicted)
EPA Substance Registry System
1,3,6-Naphthalenetrisulfonic acid (86-66-8)
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Safety

HS Code 
2904100090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H314Causes severe skin burns and eye damage

Precautionary statements

P260Do not breathe dust/fume/gas/mist/vapours/spray.

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

P310Immediately call a POISON CENTER or doctor/physician.

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N-Bromosuccinimide Price

AK Scientific
Product number
3611AC
Product name
Naphthalene-1,3,6-trisulfonicacid
Packaging
250mg
Price
$1051
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
CHM0117473
Product name
1,3,6-NAPHTHALENE TRISULFONIC ACID
Purity
95.00%
Packaging
5G
Price
$1334.03
Updated
2021/12/16
Alichem
Product number
86668
Product name
Naphthalene-1,3,6-trisulfonicacid
Packaging
1g
Price
$615.44
Updated
2021/12/16
Chemenu
Product number
CM140026
Product name
Naphthalene-1,3,6-trisulfonicacid
Purity
95%
Packaging
1g
Price
$729
Updated
2021/12/16
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Naphtalene-1,3,6-trisulfonic Acid Chemical Properties,Usage,Production

Uses

The total reaction mixture is nitrated, and the resulting 8-nitro derivative is reduced to give 1-aminonaphthalene-3,6,8-trisulfonic acid (Koch acid), the key intermediate in the production of the important H acid. The crude trisodium salt may be precipitated from the quenched mixture after dilution to 75 % acid strength to give a product (Azoguard) used as a diazo stabilizer.

Definition

ChEBI: Naphthalene-1,3,6-trisulfonic acid is a naphthalenesulfonic acid.

Production Methods

Naphthalene is initially sulfonated with sulfuric acid monohydrate under programmed temperature control between 80 and 145℃. Then, 65 % oleum is added gradually at 40℃ and heating is continued for 2.5 h at 145℃. Trisulfonation is complete after the further addition of 65 % oleum and heating for 3 h at 150℃. This complex procedure maximizes the formation of Naphtalene-1,3,6-trisulfonic Acid with a conversion of up to 75 %.

Naphtalene-1,3,6-trisulfonic Acid Preparation Products And Raw materials

Raw materials

Preparation Products

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Naphtalene-1,3,6-trisulfonic Acid Suppliers

Matrix Scientific
Tel
--
Fax
--
Email
sales@matrixscientific.com
Country
United States
ProdList
6632
Advantage
80
APAC Pharmaceutical, LLC
Tel
--
Fax
--
Email
sales@apacpharma.com
Country
United States
ProdList
6322
Advantage
38

86-66-8, Naphtalene-1,3,6-trisulfonic AcidRelated Search:


  • naphthalene-1,3,6-trisulphonic acid
  • 2,5,7-Naphthalenetrisulfonic acid
  • 86-66-8