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6440-58-0

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6440-58-0 Usage

Chemical Properties

Liquid

Uses

Different sources of media describe the Uses of 6440-58-0 differently. You can refer to the following data:
1. Dimethyloldimethyl hydantoin is used as preservative in a broad number of household and industrial cleaners to prevent spoilage from microorganisms
2. Dantogard(R) XL-1000 is a concentrated industrial preservative that can be used in a broad number of H,I&I formulations to prevent product spoilage.
3. Glydant(R) is used as antimicrobial and for the preservation of personal care formulations.
4. Glydant(R) XL-1000 is an effective cosmetic preservative.
5. Dantogard(R) 2000 one of the most advanced EPA Registered preservative on the market today.
6. Dantoserve(R) SG preservative is a cost-effective product engineered for a wide variety of household and industrial product applications to prevent product spoilage.
7. Glydant(R) 2000 is an effective cosmetic preservative. Product Data Sheet
8. Dimethyloldimethyl hydantoin is a popular preservative with moderate sensitizing potential, it is used to control against mold, mildew, and bacterial spoilage. This preservative is similar to imidazolidinyl urea, as both act by releasing formaldehyde into the formulation. Cosmetic expert panels have determined that Dimethyloldimethyl hydantoin has an excellent safety record for use in both leave-on and washoff cosmetic preparations. Maximum-use concentrations are set at 0.2 percent in the u.S. and 0.6 percent in the european union. Dimethyloldimethyl hydantoin stands for dimethylimidazolidine, though in a listing the acronym is rarely spelled out.
9. Durable and regenerable antibacterial fabrics were prepared by using an innovative chemical technology employing a precursor biocidal agent, dimethylol dimethylhydantoin (DMDMH)?, iin a chemical finishing process.

Flammability and Explosibility

Nonflammable

Check Digit Verification of cas no

The CAS Registry Mumber 6440-58-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,4 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6440-58:
(6*6)+(5*4)+(4*4)+(3*0)+(2*5)+(1*8)=90
90 % 10 = 0
So 6440-58-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H12N2O4/c1-7(2)5(12)8(3-10)6(13)9(7)4-11/h10-11H,3-4H2,1-2H3

6440-58-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Dimethyloldimethyl hydantoin

1.2 Other means of identification

Product number -
Other names 1,3-bis

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6440-58-0 SDS

6440-58-0Upstream product

6440-58-0Downstream Products

6440-58-0Relevant articles and documents

COMPOSITIONS COMPRISING BENZYL ALCOHOL DERIVATIVES AND FURTHER ANTIMICROBIAL ACTIVE COMPOUNDS

-

, (2011/07/06)

The present invention relates to a composition comprising or consisting of: (a) one, two or more compounds selected from the group consisting of benzyl alcohol derivatives of the formula (I) wherein each of the substituents R1, R2, and R3 has a position at the aromatic ring, and wherein the substituents R1, R2, and R3 independently of one another are selected from the group consisting of: H; OH; OCH3; COON; linear or branched, saturated aliphatic hydrocarbon radical having 1 to 8 carbon atoms; linear or branched, unsaturated aliphatic hydrocarbon radical having 2 to 8 carbon atoms; COOR4, wherein R4 is a linear or branched alkyl radical having 1 to 8 carbon atoms; wherein the total number of carbon atoms in substituents R1, R2 and R3 is 1 to 12, and (b) one, two or more compounds selected from the group consisting of: (i) branched or unbranched 1,2-alkanediols having 3 to 14 carbon atoms, (ii) benzoic acid (INCI: Benzoic Acid) and its esters and salts, (iii) 4-hydroxybenzoic acid and its esters (INCI: Parabens) and salts, (iv) 2,4-hexadienoic acid (INCI: Sorbic Acid) and its salts, (v) 2-phenoxyethanol (INCI: Phenoxyethanol) (vi) 3-iodo-2-propinyl-butylcarbamate (INCI: Iodopropynyl Butylcarbamate), (vii) 3-(4-chlorphenoxy)-1,2-propane-1,2-diol (INCI: Chlorphenesin), (viii) urea (INCI: Urea) and derivatives thereof, in particular 1,1′-methylen-bis(3-(1-hydroxymethyl-2,4-dioximidazolidin-5-yl))urea (INCI: Imidazolidinyl urea), N-hydroxymethyl-N-(1,3-di(hydroxymethyl)-2,5-dioxoimidazolidin-4-yl)-N′-hydroxy-methylurea (INCI: Diazolidinyl Urea) and N-(4-chlorophenyl)-N′-(3,4-dichlorophenyl)-urea (INCI: Triclocarban), (ix) 1,3-bis-(hydroxymethyl)-5,5-dimethyl-2,4-imidazolidindione (INCI: DMDM hydantoin), (x) 1,2-propanediol, 3-(2-ethylhexyloxy) (INCI: Octoxyglycerin), (xi) isothiazolinones and mixtures thereof (e.g. a mixture of 5-chloro-2-methyl-3(2H)-isothiazolinone and 2-methyl-3(2H)-isothiazolinone with magnesium chloride and magnesium nitrate; INCI: Methylchloroisothiazolinone and Methylisothiazolinone).

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