ChemicalBook > Product Catalog >Organic Chemistry >Amides >Sulfonic acids amino compound >N,N-methylenebis N'-1-(hydroxymethyl)-2,5-dioxo-4-imidazolidinyl urea

N,N-methylenebis N'-1-(hydroxymethyl)-2,5-dioxo-4-imidazolidinyl urea

N,N-methylenebis N'-1-(hydroxymethyl)-2,5-dioxo-4-imidazolidinyl urea Structure
CAS No.
130-23-4
Chemical Name:
N,N-methylenebis N'-1-(hydroxymethyl)-2,5-dioxo-4-imidazolidinyl urea
Synonyms
K ACID;Euopean K Acid;EUROPEAN K-ACID;1-Amino-8-naphthol-4,6-disulfonicaci;1-amino-8-naphtho-4,6-Disulfonic acid;1 AMINO 8 HYDROXY 4:6 DISULFONIC ACID;1-AMINO-8-NAPHTHOL-4,6-DISULFONIC ACID;8-AMINO-1-NAPHTHOL-3,5-DISULFONIC ACID;4-Amino-5-naphthol-1,7-disulfonic acid;KACID(1-AMINO-8NAPHTHO-4,6-DISULFONICACID)
CBNumber:
CB0207416
Molecular Formula:
C10H9NO7S2
Molecular Weight:
319.31
MOL File:
130-23-4.mol
MSDS File:
SDS
Modify Date:
2023/11/7 17:05:35

N,N-methylenebis N'-1-(hydroxymethyl)-2,5-dioxo-4-imidazolidinyl urea Properties

Density 1.880±0.06 g/cm3(Predicted)
pka -0.83±0.40(Predicted)
Water Solubility 20g/L at 26.4℃
LogP -2.33
CAS DataBase Reference 130-23-4(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338

N,N-methylenebis N'-1-(hydroxymethyl)-2,5-dioxo-4-imidazolidinyl urea Chemical Properties,Uses,Production

Chemical Properties

1-Amino-8-hydroxynaphthalene-4,6-disulfonic acid [130-23-4]. (4-amino-5-hydroxynaphthalene-1,7-disulfonic acid), K acid, C10H9NO7S2, Mr 319.3: the acid sodium salt of 1-Amino-8-hydroxynaphthalene-4,6-disulfonic acid is very soluble in water, but the acid potassium salt is less soluble and is more easily salted out. K acid couples under acid and alkaline conditions in a similar manner to H acid.

Uses

Azo dye intermediate.

Uses

The N-substituted derivatives of K acid, such as N-acetyl, N-benzoyl, N-(2,5-dichlorobenzoyl), and N-benzyl, are used as monoazo coupling components in special cases where an improvement in dye properties over the H acid analogue is demonstrable.

Production Methods

1-Aminonaphthalene-4,6,8-trisulfonic acid paste is heated with sodium hydroxide liquor in an autoclave at 170℃ for 12 h, after which the mixture is added to excess dilute hydrochloric acid. After heating to remove sulfur dioxide, the product (including ca. 8 % of the isomeric 5-amino-2-hydroxynaphthalene-4,8-disulfonic acid) is completely precipitated by cooling and is isolated in 86 % yield. Purification of crude K acid may be effected by dissolving it in aqueous alkali and filtering off the less soluble 5,2,4,8-isomer before reprecipitating.

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K ACID EUROPEAN K-ACID 1 AMINO 8 HYDROXY 4:6 DISULFONIC ACID 1-AMINO-8-NAPHTHOL-4,6-DISULFONIC ACID 4-amino-5-hydroxynaphthalene-1,7-disulfonic acid 4-amino-5-hydroxynaphthalene-1,7-disulphonic acid 1-amino-8-naphtho-4,6-Disulfonic acid 1-Amino-8-Naphthol-4£6-disulfonic acid/European K Acid 8-AMINO-1-NAPHTHOL-3,5-DISULFONIC ACID 4-Amino-5-hydroxy-1,7-naphthalenedisulfonic acid 4-Amino-5-naphthol-1,7-disulfonic acid KACID(1-AMINO-8NAPHTHO-4,6-DISULFONICACID) 4-azanyl-5-hydroxy-naphthalene-1,7-disulfonic acid N,N-methylenebis N'-1-(hydroxymethyl)-2,5-dioxo-4-imidazolidinyl 1,7-Naphthalenedisulfonic acid, 4-amino-5-hydroxy- 1-Amino-8-naphthol-4,6-disulfonicaci N,N-methylenebis N'-1-(hydroxymethyl)-2,5-dioxo-4-imidazolidinyl urea ISO 9001:2015 REACH Euopean K Acid 130-23-4 Intermediates of Dyes and Pigments