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Acid Red 73

Acid Red 73 structure

Acid Red 73 

structure
  • CAS No:

    5413-75-2

  • Formula:

    C22H16N4O7S2.2Na

  • Chemical Name:

    Acid Red 73

  • Synonyms:

    1,3-Naphthalenedisulfonic acid,7-hydroxy-8-[2-[4-(2-phenyldiazenyl)phenyl]diazenyl]-,sodium salt (1:2);C.I. Acid Red 73,disodium salt;C.I. Acid Red 73;1,3-Naphthalenedisulfonic acid,7-hydroxy-8-[[4-(phenylazo)phenyl]azo]-,disodium salt;Croceine Scarlet MOO;C.I. 27290;Acidal Bright Croceine;Acid Fast Red RN;Acid Leather Red PSNR;Acid Red 73;Acilan Croceine MOO;Airedale Scarlet MO;Amacid Brilliant Croceine 3BA;Atul Croceine Scarlet MOO;Brilliant Croceine;Brilliant Croceine 3BA-CF;Brilliant Croceine LBH;Brilliant Croceine MO;Brilliant Croceine MOO;Brilliant Croceine MOOL;Brilliant Croceine Scarlet M;Brilliant Croceine Scarlet N;Brilliant Croceine SWW;Brilliant Red 2EMBL;Brilliant Red EMBL;Brilliant Scarlet R;Brilliant Scarlet LC;Calcocid Scarlet MOON;Croceine Brilliant Scarlet 3BC;Croceine Brilliant Scarlet 3BS;Croceine Scarlet M;Croceine Scarlet 3B;Croceine Scarlet MOON;Croceine Scarlet SS;Crocein Scarlet N;Crocein Scarlet MOO;Curol Brilliant Red G;Eniacid Brilliant Scarlet;Erionyl Red E-GR;Eriosin Red GR;Fenazo Red XG;Hidacid Brilliant Crocein Scarlet;Hispacid Scarlet M;Java Brilliant Scarlet MOO;Kiton Fast Scarlet A;Kiton Scarlet MOO;Brilliant Croceine M;Brilliant Croceine P;Brilliant Croceine 3B;Brilliant Croceine 3BM;Oxanal Scarlet A;Paper Scarlet R;Paper Scarlet A extra;Paper Scarlet WEG;Ponceau PSNR;Scarlet MOO;Tertracid Brilliant Croceine MOO;Vondacid Light Scarlet MOO;61813-60-3;77466-28-5;84842-89-7;188763-03-3

  • Categories:

    Cosmetic Ingredient  >  Cosmetic Colorant

Description

ChEBI: An organic sodium salt that is the disodium salt of 7-hydroxy-8-{[4-(phenyldiazenyl)phenyl]diazenyl}naphthalene-1,3-disulfonic acid. Occasionally used for the demonstration of muscle fibres in conjunction with, or as a replacement for, acid fuchsin.


Woodstain scarlet is an organic sodium salt that is the disodium salt of 7-hydroxy-8-{[4-(phenyldiazenyl)phenyl]diazenyl}naphthalene-1,3-disulfonic acid. Occasionally used for the demonstration of muscle fibres in conjunction with, or as a replacement for, acid fuchsin. It has a role as a histological dye. It contains a 7-hydroxy-8-{[4-(phenyldiazenyl)phenyl]diazenyl}naphthalene-1,3-disulfonate.

Acid Red 73 Basic Attributes

556.48

556.009949

226-502-1

5PLA82FV3C

DTXSID1041712

3204120000

Characteristics

200.83000

7.34600

red powder

1.58g/cm3

soluble in water

Safety Information

NONH for all modes of transport

3

20/21/22-36/37/38

22-24/25-36-26

Xn

|Warning|H302 (37.5%): Harmful if swallowed [Warning Acute toxicity, oral]|P201, P202, P261, P264, P270, P271, P272, P273, P280, P281, P301+P312, P302+P352, P304+P340, P305+P351+P338, P308+P313, P312, P321, P330, P332+P313, P333+P313, P337+P313, P362, P363, P403+P233, P405, and P501|Aggregated GHS information provided by 56 companies from 7 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.|H351: Suspected of causing cancer [Warning Carcinogenicity]|P201, P202, P281, P308+P313, P405, and P501

Drug Information

acid red 73

Acid Red 73 Use and Manufacturing

Methods of Manufacturing

It is obtained by diazotizing p-aminoazobenzene, coupling with G salt, and salting out. 1. Diazotization: Add 240kg of p-aminoazobenzene hydrochloride to 1200L of water, and add 200kg of 30% hydrochloric acid. Stir for 4 hours, cool to 8°C, add 30% sodium nitrite solution (100% 80 kg) from below the liquid surface within 3 hours, the temperature does not exceed 15°C, with a slight excess of nitrous acid as the end point, keep it for 1 hour, add ice cooling to 5 Below ℃, filter, discard the filter residue, add salt to the filtrate by volume 28%, stir for 20min, filter, the filter cake is diluted with water and ice to 3000L, the temperature is 0-5℃. 2. Coupling Put 1500L of water and 160kg of soda ash in the barrel, stir, add 270kg of G salt to make it completely dissolved. Cool to 5°C, add the above-mentioned diazonium liquid within 3h, and the temperature should not exceed 12°C. After the addition, the pH should be 9 and the G salt is excessive. After stirring for 6 hours, the temperature was raised to 60°C, salt was added by 9% by volume, filtered, and dried to obtain 680 kg of the original dye. After standardization, the finished dye is 1000kg. G salt (100%) 280 sodium nitrite (98%) 82 p-aminoazobenzene (100%) 248 hydrochloric acid (31%) 196 sodium carbonate (98%) 157 yuan Ming powder 160

Uses

Mainly used for dyeing wool, silk fabrics, paper and leather, but also for coloring plastics, anodized aluminum and cement

1,3-Naphthalenedisulfonic acid, 7-hydroxy-8-[2-[4-(2-phenyldiazenyl)phenyl]diazenyl]-, sodium salt (1:2): ACTIVE

Cosmetics -> Hair dyeing

Computed Properties

Molecular Weight:556.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:11
Rotatable Bond Count:4
Exact Mass:556.00992971
Monoisotopic Mass:556.00992971
Topological Polar Surface Area:201
Heavy Atom Count:37
Complexity:952
Covalently-Bonded Unit Count:3
Compound Is Canonicalized:Yes

Material

SODIUM SULFATE

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