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35691-65-7

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35691-65-7 Usage

Description

1,2-Dibromo-2,4-dicyanobutane is the main sensitizer of Euxyl K400, a widely used preservative agent in cosmetics, toiletries or metalwork fluids. Methyldibromo glutaronitrile (MDBGN), also known as dibromocyanobutane, is to be found in the preservative system Euxyl K 400 (also called Tektamer 38), which is a mix of MDBGN and phenoxyethanol in a ratio of 1:4. Euxyl K 400 is a broad‐spectrum preservative with activity against fungi and bacteria. MDBGN is nearly always the allergen when sensitization to Euxyl K 400 occurs.

Chemical Properties

Light yellow crystalline solid or powder. Commercial products may be soluble concentrate (liquid or solid); pellets/tablets. Mild, acrid, sweet odor.

Occurrence

MDBGN was historically widely used in cosmetics, sunscreens, shampoos, liquid soaps, and barrier and moisturizing creams used at work. Other sources include moistened toilet tissues, ultrasound gel, adhesives, soluble cutting oils, latex paints, vaginal examination gel and sanitary pads. The EU ban has reduced these exposures very signifi cantly. Nevertheless, its inclusion in products used in the workplace such as barrier creams and after‐work creams makes its inclusion in the European and BSCA baseline series still relevant at the current time.

Uses

1,2-Dibromo-2,4-dicyanobutane is a preservative for metalworking fluids, cosmetics, adhesives, latex emulsions and paints, dispersed pigments and detergents; active ingredient in Euxyl K 400 and Tektamer 38.

Definition

ChEBI: An organobromine compound that consists of pentanedinitrile bearing bromo and bromomethyl substituents at position 2.

General Description

Crystals with a pungent odor. Insoluble in water. Used as a preservative in latex paint, adhesives, etc.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

DBDCB may polymerize in the presence of metals and some metal compounds. Incompatible with acids; mixing nitriles with strong oxidizing acids can lead to extremely violent reactions. Nitriles are generally incompatible with other oxidizing agents such as peroxides and epoxides. The combination of bases and nitriles can produce hydrogen cyanide. Nitriles are hydrolyzed in both aqueous acid and base to give carboxylic acids (or salts of carboxylic acids). These reactions generate heat. Peroxides convert nitriles to amides. Nitriles can react vigorously with reducing agents.

Agricultural Uses

Microbiocide: Tolerances have been established by the U.S. Food and Drug Administration when this substances is used as a preservative in food-grade adhesives and as a slimicide in the manufacture of food-grade paper and paperboard. Used to control slime-forming bacteria and fungi in recirculating water cooling system; oil-recovery drilling mud systems; paper mill and pulp mill water systems and similar industrial processing and chemical systems.

Trade name

BIOCHEK?; BIOCLEAR?; MERCK? 48051; METACIDE? 38; METASOL; TEKTAMER

Contact allergens

Methyldibromo glutaronitrile is a biocide widely used as a preservative agent in cosmetics, toiletries, and metalworking fluids. It is a potent allergen, banned in all cosmetics in the EU since 2007.

Safety Profile

Experimental reproductive effects. When heated to decomposition it emits toxic fumes of NO, and Br-.

Potential Exposure

Nitrile microbiocide used as a preser- vative in food grade adhesives and as a slimicide in the manufacture of food grade paper and paperboard; used to control slime-forming bacteria and fungi in recirculating water cooling system; oil recovery drilling mud systems; paper mill and pulp mill water systems and similar indus- trial processing and chemical systems.

Shipping

UN3261 Corrosive solid, acidic, organic, n.o.s., Hazard class: 8; Labels: 8-Corrosive material, Technical Name Required. UN3439 Nitriles, solid, toxic, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required.

Incompatibilities

Corrosive. Strong oxidizers and reducing agents, strong acids and bases. Reacts with acids, steam, warm water producing toxic and flammable hydrogen cya- nide fumes. Hydrogen cyanide is produced when propioni- trile is heated to decomposition. Nitriles may polymerize in the presence of metals and some metal compounds. They are incompatible with acids; mixing nitriles with strong oxidizing acids can lead to extremely violent reactions. Nitriles are generally incompatible with other oxidizing agents such as peroxides and epoxides. The combination of bases and nitriles can produce hydrogen cyanide. Nitriles are hydrolyzed in both aqueous acid and base to give car- boxylic acids (or salts of carboxylic acids). These reactions generate heat. Peroxides convert nitriles to amides. Nitriles can react vigorously with reducing agents. Acetonitrile and propionitrile are soluble in water, but nitriles higher than propionitrile have low aqueous solubility. They are also insoluble in aqueous acids .

Check Digit Verification of cas no

The CAS Registry Mumber 35691-65-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,6,9 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 35691-65:
(7*3)+(6*5)+(5*6)+(4*9)+(3*1)+(2*6)+(1*5)=137
137 % 10 = 7
So 35691-65-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H6Br2N2/c7-4-6(8,5-10)2-1-3-9/h1-2,4H2

35691-65-7 Well-known Company Product Price

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  • Price
  • Detail
  • Alfa Aesar

  • (L18725)  1,2-Dibromo-2,4-dicyanobutane, 99%   

  • 35691-65-7

  • 25g

  • 487.0CNY

  • Detail
  • Alfa Aesar

  • (L18725)  1,2-Dibromo-2,4-dicyanobutane, 99%   

  • 35691-65-7

  • 100g

  • 1432.0CNY

  • Detail

35691-65-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-2-(bromomethyl)pentanedinitrile

1.2 Other means of identification

Product number -
Other names 1-Bromo-1-(bromomethyl)-1,3-propanedicarbonitrile

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:35691-65-7 SDS

35691-65-7Synthetic route

2,4-dicyano-1-butene
1572-52-7

2,4-dicyano-1-butene

1,2-Dibromo-2,4-dicyanobutane
35691-65-7

1,2-Dibromo-2,4-dicyanobutane

Conditions
ConditionsYield
With bromine Irradiation;
acrylonitrile
107-13-1

acrylonitrile

1,2-Dibromo-2,4-dicyanobutane
35691-65-7

1,2-Dibromo-2,4-dicyanobutane

Conditions
ConditionsYield
Stage #1: acrylonitrile With triethylamine; zinc(II) chloride for 1h; Autoclave; Green chemistry; Large scale;
Stage #2: With bromine In water at 50 - 100℃; for 2h; Green chemistry; Large scale;
510 kg
1,2-Dibromo-2,4-dicyanobutane
35691-65-7

1,2-Dibromo-2,4-dicyanobutane

2,4-dicyano-1-butene
1572-52-7

2,4-dicyano-1-butene

Conditions
ConditionsYield
In acetonitrile Product distribution; Mechanism; other solvents;

35691-65-7Downstream Products

35691-65-7Relevant articles and documents

Green production technology for bromothalonil

-

Paragraph 0018; 0019, (2017/01/26)

The invention provides a green production technology for bromothalonil. The technology has the advantages that operation is easy, the production process is green and free of pollutant discharge, used solvent can be recycled and reused, the product yield is high, the production cost is effectively reduced, energy is saved, consumption is reduced, and the obtained bromothalonil is high in content, good in crystal form and low in color number and can be combined with multiple bactericides to form a sterilization composition, and effectively inhibit and eradicate growth of bacteria, fungi and algae.

Microbicidal mixtures

-

, (2008/06/13)

The invention relates to synergistic mixtures of methyl-2H-isothiazol-3-one and 2-bromo-2-nitropropanediol for controlling microorganisms in industrial materials.

Aqueous isothiazolone formulation

-

, (2008/06/13)

An aqueous isothiazolone formulation useful for antiseptic or antifungal treatment of various synthetic polymeric emulsions, which comprises (a) a specific isothiazolone compound, (b) water or an aqueous solvent and (c) a specific nitrobromo or cyanobromo compound.

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