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ADH (ADIPIC ACID DIHYDRAZIDE)

ADH (Adipic acid dihydrazide) is a symmetrical molecule with a C4 backbone, and the reactive group is C=ONHNH2. 
ADH (Adipic acid dihydrazide) finds major applications as a latent curing agent for B-stageable epoxy resins and as an ambient temperature crosslinking agent for high-performance acrylic emulsion architectural coatings. 
ADH (Adipic acid dihydrazide) is also employed as a paint additive and coating additive.

CAS Number: 1071-93-8
EC Number: 213-999-5
IUPAC Name: Hexanedihydrazide
Chemical Formula: C6H14N4O2

Other names: Adipic dihydrazide, 1071-93-8, Adipohydrazide, Adipic acid dihydrazide, Hexanedihydrazide, Hexanedioic acid, dihydrazide, Adipic acid, dihydrazide, Adipoyldihydrazine, adipoyl dihydrazide, MFCD00007614, VK98I9YW5M, DTXSID0044361, Hexanedioic acid, 1,6-dihydrazide, NSC-3378, NSC-29542, WLN: ZMV4VMZ, Adipyl hydrazide, Adipodihydrazide, Adip dihydr, adipic hydrazide, Adipoyl hydrazide, adipic dihydrazone, Hexanedihydrazide #, NSC 3378, EINECS 213-999-5, NSC 29542, Adipic acid dihyrazide, Hexanedioic dihydrazide, AJICURE ADH, QUALIMER ADH, AI3-22640, ULTRALINK HYDRAZIDE, UNII-VK98I9YW5M, EC 213-999-5, Hexanedioic acid dihydrazide, SCHEMBL49856, CHEMBL3185968, DTXCID8024361, SCHEMBL11037942, NSC3378, 1,4-Butanedicarboxylic dihydrazide, ALBB-011767, BK 1000Z, BT 1000Z, NSC29542, STR02658, Tox21_301067, BBL022965, STK709135, AKOS000267183, NCGC00248276-01, NCGC00257525-01, CAS-1071-93-8, DB-022418, A0170, Adipic acid dihydrazide, >=98% (titration), CS-0010116, NS00003709, EN300-03706, D72486, T 2210, Adipic acid dihydrazide, purum, >=97.0% (NT), Q4682936, Z56812730, F1943-0024, InChI=1/C6H14N4O2/c7-9-5(11)3-1-2-4-6(12)10-8/h1-4,7-8H2,(H,9,11)(H,10,12), ADH, ADIPINIC DIHYDRAZIDE, ADIPIC DIHYDRAZIDE, ADIPIC ACID DIHYDRAZIDE, ADIPIC ACID DIHYDRIZIDE, adipoyl hydrazide, ADIPODIHYDRAZIDE;Adipohydrazide

ADH (Adipic acid dihydrazide) serves as a difunctional crosslinking agent in paints and coatings applied to specific water-based acrylic emulsions. 
ADH (Adipic acid dihydrazide) acts as a hardener for epoxy resins and a chain extender for polyurethanes. 
Moreover, it finds a minor application as a formaldehyde scavenger, preventing the release of formaldehyde.

ADH (Adipic acid dihydrazide) is used as a formaldehyde scavenger and reacts with formaldehyde, thereby preventing the volatilizing of formaldehyde in the air.
ADH (Adipic acid dihydrazide) is also used as an intermediate.
Materials crosslinked or cured with ADH demonstrate excellent colour stability, weathering resistance, adhesion, durability, hardness, and toughness.

ADH (Adipic acid dihydrazide) is a chemical used for cross-linking water-based emulsions.
ADH (Adipic acid dihydrazide) can also be used as a hardener for certain epoxy resins.
ADH (Adipic acid dihydrazide) is used in the linking of glycoproteins, such as antibodies, in a site specic fashion following periodate oxidation.

ADH (Adipic acid dihydrazide) is a chemical used for cross-linking water-based emulsions.
ADH (Adipic acid dihydrazide) can also be used as a hardener for certain epoxy resins.
ADH (Adipic acid dihydrazide) is a symmetrical molecule with a C4 backbone and the reactive group is C=ONHNH2.

ADH (Adipic acid dihydrazide) are made by the reaction of an organic acid with hydrazine.
ADH (Adipic acid dihydrazide) with dierent backbones are also common, including isophthalic dihydrazide (IDH) and sebacic dihydrazide (SDH).
A notable fact with regard to ADH (Adipic acid dihydrazide) in epoxy formulations is that each of the primary amine end groups has a functionality of two, so the ADH molecule has an equivalency of four per epoxy moiety.

Accordingly, the active hydrogen equivalent weight of ADH (Adipic acid dihydrazide) is 43.5.
When formulated with epoxy resins, the ADH (Adipic acid dihydrazide) index can range between 0.85-1.15 of stoichiometric proportions, without a signicant eect on mechanical properties.
The cure temperature for epoxy resins (glycidyl types) formulated with ADH (Adipic acid dihydrazide) is inuenced by the melt-out temperature of the ADH, which allows an extended pot life at low temperatures.

Storage stability can be up to six-months at room temperature, with cure times of about one-hour at 130 °C.
Cure rates can be accelerated using tin or titanate catalysts, or imidazoles.
One-component ADH (Adipic acid dihydrazide) epoxy systems can be partially cured or “B-staged”, and later fully cured.

ADH (Adipic acid dihydrazide) is an eective room temperature curative for solution polyurethanes.
ADH (Adipic acid dihydrazide) provides polyurea coatings with higher hardness, toughness and adhesion properties, excellent mechanical properties, abrasion and chemical resistance.
ADH (Adipic acid dihydrazide) cured polyurethane coatings exhibit good color stability and weathering properties, which is not observed with standard amine curatives.

ADH (Adipic acid dihydrazide), white crystalline solid, with symmetrical molecular structure, is double-functional group compound.
ADH (Adipic acid dihydrazide) is a kind of good crosslinking agent, can be crosslinked with carbonyl, more typically has and is applied to medicine and pharmacology with cross-linking hyaluronic acid.

ADH (Adipic acid dihydrazide) is a homobifunctional cross-linking reagent specic for aldehydes resulting in relatively stable hydrazone linkages.
ADH (Adipic acid dihydrazide) is typically, used in the linking of glycoproteins, such as antibodies, in a site specic fashion following periodate oxidation.
ADH (Adipic acid dihydrazide) is used for cross-linking water-based emulsions and as a hardener for certain epoxy resins, which nds application in powder coating.

Adipic dihydrazides (C6H14N4O2) are made by the reaction of an organic acid with hydrazine. Other dihydrazides with different backbones are also common, including isophthalic dihydrazide (IDH) and sebacic dihydrazide (SDH).
ADH (Adipic acid dihydrazide) is a distinctive crosslinking agent and curative that provides controlled reactivity and performance improvements in epoxy resins, polyurethane dispersions (PUDs), solvent-based polyurethanes (PURs), and emulsion acrylic resins. 

ADH (Adipic acid dihydrazide) is the most suitable hydrazide cross-linking agent, and ADH has been widely used in water-based paint emulsions in combination with diacetone acrylamide. 
ADH (Adipic acid dihydrazide) is commonly used as a crosslinking agent in water-based coatings, adhesives, and epoxy resins, enhancing durability and flexibility. 
Additionally, ADH (Adipic acid dihydrazide) serves as an intermediate in pharmaceuticals, textiles, and polymer chemistry. 

The compound appears as a white crystalline powder, is relatively stable under normal conditions, and is soluble in water and certain organic solvents. 
Due to its bifunctional reactive sites, it participates in various condensation and polymerization reactions.
ADH (Adipic acid dihydrazide) is a chemical used for cross-linking water-based emulsions. 

It can also be used as a hardener for certain epoxy resins.
ADH (Adipic acid dihydrazide) is weakly alkaline, and there is a possibility of agglomeration when solid ADH is added directly to the emulsion, so usually ADH should be dissolved in hot water before use.
ADH (Adipic acid dihydrazide) is an organic compound derived from adipic acid, where both carboxyl groups (-COOH) are replaced by hydrazide (-CONHNH₂) functional groups. 

Melting point: 180-182 °C (lit.)
Boiling point: 305.18°C (rough estimate)
Density: 1.2297 (rough estimate)
vapor pressure: 0Pa at 25℃
refractive index: 1.6700 (estimate)
Flash point: 150 °C
storage temp.: -20°C
solubility: H2O: 100 mg/mL
form: Crystalline Powder
pka: 12.93±0.35(Predicted)
color: White to slightly yellow
Water Solubility: soluble
BRN: 973863
InChIKey: IBVAQQYNSHJXBV-UHFFFAOYSA-N
LogP: -2.7 at 20℃
CAS DataBase Reference: 1071-93-8(CAS DataBase Reference)
EWG's Food Scores: 1-3

ADH (Adipic acid dihydrazide) is an eective crosslinking agent, curative and hardener.
ADH (Adipic acid dihydrazide) is the most common dihydrazide crosslinking agent within a series of dihydrazides such as sebacic dihydrazide (SDH) and isophthalic dihydrazide (IDH).
ADH (Adipic acid dihydrazide)’s has a melting point of 180 °C and a molecular weight of 174; both are lower than the alternative dihydrazides SDH and IDH.

ADH (Adipic acid dihydrazide) is a low molecular weight compound that comprises a hydrazide group at each end. 
This leads to the supply of extra adsorption sites for heavy metals that maintain or elevate the adsorption capacities of the cross-linked adsorbents. 
ADH (Adipic acid dihydrazide) is used as a crosslinker in various fields, like making mechanical latexes films and injectable oxidized hyaluronic acid hydrogel.

ADH (Adipic acid dihydrazide) is an organic compound with the molecular formula C₆H₁₄N₄O₂, derived from adipic acid (a common dicarboxylic acid) by replacing both carboxyl (-COOH) groups with hydrazide (-CONHNH₂) functional groups. 
This modification gives ADH its unique reactivity, making it an important crosslinking agent, curing agent, and chemical intermediate in various industries.

ADH (Adipic acid dihydrazide) is a homobifunctional cross-linking reagent that is specific for aldehydes. 
This results in relatively stable hydrazone linkages. 
ADH (Adipic acid dihydrazide) is generally used in the linking of glycoproteins, like antibodies, in a site-specific fashion following periodate oxidation. 

Oxidation and coupling may be performed at pH 5.0 due to the low pKa of the hydrazide which avoids competition by primary amines.
ADH (Adipic acid dihydrazide) is a chemical used for cross-linking water-based emulsions.
ADH (Adipic acid dihydrazide) can also be used as a hardener for certain epoxy resins.

ADH (Adipic acid dihydrazide) is a symmetrical molecule with a C4 backbone and the reactive group is C=ONHNH2.
Dihydrazides are made by the reaction of an organic acid with hydrazine.
ADH (Adipic acid dihydrazide) with dierent backbones are also common, including isophthalic dihydrazide (IDH) and sebacic dihydrazide (SDH).

ADH (Adipic acid dihydrazide) is pure white crystals.
ADH (Adipic acid dihydrazide) is easily soluble in water and poisoned.
ADH (Adipic acid dihydrazide) is used as epoxy powder coating curing agent and coating additive, metal deactivator and other polymer additives and water treatment agent.

ADH (Adipic acid dihydrazide) is a homobifunctional cross-linking reagent that is specic for aldehydes.
This results in relatively stable hydrazone linkages.

ADH (Adipic acid dihydrazide) is generally used in the linking of glycoproteins, like antibodies, in a site-specic fashion following periodate oxidation.
Oxidation and coupling may be performed at pH 5.0 due to the low pKa of the hydrazide which avoids competition by primary amines.

Uses Of ADH (Adipic acid dihydrazide):
ADH (Adipic acid dihydrazide) is used for cross-linking water-based emulsions and as a hardener for certain epoxy resins, which nds application in powder coating.
ADH (Adipic acid dihydrazide) is used to functionalize magnetic nanoparticles for gylcopeptitde enrichment and identication.
ADH (Adipic acid dihydrazide) can also be used as a chain extension for liquid rubber.

ADH (Adipic acid dihydrazide) is a chemcial intermediate and specialty chemical often used in adhesive and coatingmanufacturing applications.
ADH (Adipic acid dihydrazide) oers amino- and keto-functionality at either end of the molecule which makes it an excellent cross-linking agent for water-based emulsions.
Adipic dihydrazide is used as a difunctional crosslinking agent in paints and coatings for certain water-based acrylic emulsions.  

It is used as a hardener for epoxy resins and a chain extender for polyurethanes.  
A small use is as a formaldehyde scavenger preventing the liberation of formaldehyde.
ADH (Adipic acid dihydrazide) is widely used as a crosslinker in water-based coatings, paints, and adhesives, where it reacts with ketone or aldehyde-based resins to form strong, durable bonds.

It improves water resistance, adhesion, and mechanical strength in industrial coatings, helping prevent cracking and wear over time.
ADH (Adipic acid dihydrazide) is an essential curing agent in epoxy resins used in automotive, aerospace, and construction applications.
It enhances the flexibility, toughness, and thermal stability of polymers, making it ideal for high-performance coatings and composites.

The hydrazide groups in ADH (Adipic acid dihydrazide) enable it to act as an intermediate in pharmaceutical synthesis, particularly in the development of hydrazone-based drugs used for antibacterial, anticancer, and antiviral applications.
ADH (Adipic acid dihydrazide) is used in textile finishing agents to enhance the wrinkle resistance, water repellency, and durability of fabrics.
In the paper industry, it is utilized in coating formulations to improve strength and printability.

ADH (Adipic acid dihydrazide) is used in water treatment as a chelating agent, helping to remove metal ions from industrial wastewater.
It serves as a precursor in synthesizing other hydrazide derivatives for applications in agrochemicals, dyes, and specialty chemicals.
ADH (Adipic acid dihydrazide) reacts readily with aldehydes and ketones, forming hydrazone linkages, which is useful in crosslinking applications.

It is low in toxicity but should be handled with care, as prolonged exposure to fine powder dust may cause respiratory or skin irritation.
Storage in a cool, dry place is recommended to maintain its stability and prevent premature degradation.
ADH (Adipic acid dihydrazide) is a versatile chemical with applications ranging from coatings and adhesives to pharmaceuticals and textiles. 

Its ability to form strong crosslinked structures makes it invaluable in various industrial processes, while its reactivity with aldehydes and ketones enables its use in chemical synthesis. 
As industries continue to develop high-performance materials, ADH (Adipic acid dihydrazide) remains a crucial component in advancing polymer science, material engineering, and pharmaceutical innovation.

ADH (Adipic acid dihydrazide) is used as a formaldehyde scavenger and reacts with formaldehyde, thereby preventing the volatilizing of formaldehyde in the air. 
ADH (Adipic acid dihydrazide) is also employed as a paint additive and coating additive. 
It is also used as an intermediate. 

ADH (Adipic acid dihydrazide) is used for cross-linking water-based emulsions and as a hardener for certain epoxy resins, which finds application in powder coating.
ADH (Adipic acid dihydrazide) is a homobifunctional cross-linking reagent specific for aldehydes resulting in relatively stable hydrazone linkages. 
ADH (Adipic acid dihydrazide) is typically, used in the linking of glycoproteins, such as antibodies, in a site specific fashion following periodate oxidation. 

Oxidation and coupling may conveniently be performed at pH 5.0 due to the low pKa of the hydrazide which avoids competition by primary amines.
ADH (Adipic acid dihydrazide) is soluble in water, alcohol and acetone.
ADH (Adipic acid dihydrazide) is commonly used in the linking of glycoproteins, such as antibodies, in a site specic fashion following periodate oxidation.

ADH (Adipic acid dihydrazide) is the most suitable hydrazide cross-linking agent, and ADH has been widely used in waterbased paint emulsions in combination with diacetone acrylamide. 
ADH (Adipic acid dihydrazide) is weakly alkaline, and there is a possibility of agglomeration when solid ADH is added directly to the emulsion, so usually ADH should be dissolved in hot water before use.
ADH (Adipic acid dihydrazide) is used as a formaldehyde scavenger and reacts with formaldehyde, thereby preventing the volatilizing of formaldehyde in the air.

ADH (Adipic acid dihydrazide) is also employed as a paint additive and coating additive.
ADH (Adipic acid dihydrazide) is also used as an intermediate.

Safety Profile Of ADH (Adipic acid dihydrazide):
Prolonged or repeated exposure can lead to dryness and redness.
Wear protective gloves and wash hands thoroughly after handling.
Can cause temporary eye irritation, redness, and discomfort if it comes into direct contact with the eyes.

Wear safety goggles when handling large quantities if exposure occurs, rinse eyes with plenty of water for at least 15 minutes.
While ADH (Adipic acid dihydrazide) is not highly toxic, swallowing large amounts can lead to nausea, vomiting, or gastrointestinal discomfort.
Do not eat, drink, or smoke while handling the material if ingested, seek medical attention.

While ADH (Adipic acid dihydrazide) is generally considered a low-toxicity chemical, proper handling and precautionary measures should be taken, as it can pose potential hazards in certain conditions.
Dust or powder may cause respiratory irritation if inhaled in large quantities.
Symptoms may include coughing, shortness of breath, and throat irritation.

Use appropriate ventilation and wear a dust mask when handling the powder.
Direct contact with ADH (Adipic acid dihydrazide) may cause mild skin irritation or an allergic reaction in sensitive individuals.

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