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Glutaric Dialdehyde

CAS No.
111-30-8
Chemical Name:
Glutaric Dialdehyde
Synonyms
Gluteraldehyde;glutaral;GLUTARIC DIALDEHYDE;1,5-PENTANEDIAL;Pentanedial;GDA;GLUTARDIALDEHYDE;Aqucar;PENTANDIAL;GLUTARADEHYDE
CBNumber:
CB00124029
Molecular Formula:
C5H8O2
Molecular Weight:
100.12
MDL Number:
MFCD00007025
MOL File:
111-30-8.mol
Last updated:2024-10-28 16:48:35

Glutaric Dialdehyde Properties

Melting point -15 °C
Boiling point 100 °C
Density 1.058 g/mL at 20 °C
vapor density 1.05 (vs air)
vapor pressure 15 mmHg ( 20 °C)
refractive index n20/D 1.450
Flash point 100°C
storage temp. Store below +30°C.
solubility Chloroform (Slightly), DMSO (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
form Solution
color Clear to slight haze
Specific Gravity 1.06
PH >3.0 (H2O, 20°C)
Odor pungent aldehyde odor
Water Solubility miscible
Merck 14,4472
BRN 605390
Exposure limits Ceiling (ACGIH) 0.8 mg/m3 (0.2 ppm).
Stability Light Sensitive
InChIKey SXRSQZLOMIGNAQ-UHFFFAOYSA-N
LogP -0.180 (est)
Substances Added to Food (formerly EAFUS) GLUTARALDEHYDE
FDA 21 CFR 173.357; 175.105; 176.300
CAS DataBase Reference 111-30-8(CAS DataBase Reference)
EWG's Food Scores 3-6
FDA UNII T3C89M417N
NIST Chemistry Reference Glutaral(111-30-8)
EPA Substance Registry System Glutaraldehyde (111-30-8)
Pesticides Freedom of Information Act (FOIA) Glutaraldehyde,Sporicidin

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
GHS05,GHS06,GHS08,GHS09
Signal word  Danger
Hazard statements  H301+H331-H312-H314-H317-H334-H335-H411
Precautionary statements  P261-P273-P280-P303+P361+P353-P304+P340+P310-P305+P351+P338
Hazard Codes  T,N,Xn
Risk Statements  36/37/38-42/43-34-23-22-50-23/25-41-37/38-20/22
Safety Statements  23-26-36/37-45-36/37/39-61
RIDADR  UN 2922 8/PG 2
OEL Ceiling: 0.2 ppm (0.8 mg/m3) (Aldehydes)
WGK Germany  3
RTECS  MA2450000
8-10-23
TSCA  Yes
HazardClass  8
PackingGroup  II
HS Code  29121900
Toxicity LD50 of 25% soln orally in rats: 2.38 ml/kg; by skin penetration in rabbits: 2.56 ml/kg (Smyth)
NFPA 704
0
3 0

Glutaric Dialdehyde price More Price(61)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich W512303 Glutaric dialdehyde solution 50?wt. % in H2O, FCC 111-30-8 1kg $80.5 2024-03-01 Buy
Sigma-Aldrich W512303 Glutaric dialdehyde solution 50?wt. % in H2O, FCC 111-30-8 10Kg $435 2024-03-01 Buy
Sigma-Aldrich 8.20603 Glutardialdehyde (25% solution in water) for synthesis 111-30-8 100mL $36.1 2024-03-01 Buy
Sigma-Aldrich 8.20603 Glutardialdehyde (25% solution in water) for synthesis 111-30-8 1L $56.3 2024-03-01 Buy
Sigma-Aldrich 8.20603 Glutardialdehyde (25% solution in water) for synthesis 111-30-8 2.5L $122 2024-03-01 Buy
Product number Packaging Price Buy
W512303 1kg $80.5 Buy
W512303 10Kg $435 Buy
8.20603 100mL $36.1 Buy
8.20603 1L $56.3 Buy
8.20603 2.5L $122 Buy

Glutaric Dialdehyde Chemical Properties,Uses,Production

Uses

As broad-spectrum antimicrobial cold sterilant/disinfectant for hospital equipment; as tanning agent for leather; as tissue fixative; as cross-linking agent for proteins; as preservative in cosmetics; as therapeutic agent for warts, hyperhidrosis, and dermal mycotic infections; in X ray processing solutions and film emulsion; as a disinfectant in the beauty industry

Description

Glutaraldehyde is a well-known sensitizer among cleaners and health workers. It is also found in X-ray developers products.

Chemical Properties

Glutaraldehyde is a colorless liquid with a pungent odor, which readily changes to a glossy polymer. The Odor Threshold is 0.04 ppm (NY) and 0.2 ppm (NJ). It is miscible in water and organic solvents. Glutaraldehyde may be incompatible with strong oxidizers and strong bases. It should be noted that alkaline solutions containing glutaraldehyde may react with alcohol, ketones, amines, hydrazines, and proteins.
Glutaraldehyde

Uses

Glutaraldehyde is used to disinfect medical and dental equipment. Glutaraldehyde is also used for industrial water treatment and as a preservative.

Uses

glutaral (glutardialdehyde) is a broad-spectrum preservative that can cause skin irritation. This is an amino acid occurring in green sugar beets.

Uses

Glutaraldehyde is used as a cold sterilizingdisinfectant, as fixatives for tissues, in tanning,and in cross-linking proteins.

Uses

Glutaraldehyde (Symbol GTA; glutaric dialdehyde, 1,5-pentanedial, glutaral) is commonly used in the medical industry in cold sterilization and in the X-ray development process. It can also be encountered in the leather industry as a tanning ingredient and in mortuary workers. There are no reports which indicate that glutaraldehyde is a naturally occurring compound. Cidex and Acusol, 2% buffered solutions, use this aldehyde as an active ingredient. Sodium bicarbonate is required to activate the solution, which then has a shelf life of 1–2 weeks. Despite health hazards involved with its use, glutaraldehyde is one of the most effective biocides used. It is particularly effective against bacteria and viruses, including the human immunodeficiency virus.

Definition

ChEBI: A dialdehyde comprised of pentane with aldehyde functions at C-1 and C-5.

Synthesis Reference(s)

Tetrahedron, 48, p. 3503, 1992 DOI: 10.1016/S0040-4020(01)88489-1

General Description

Light yellow liquid. Mixes with water.

Air & Water Reactions

Polymerizes in the presence of water.

Reactivity Profile

GLUTARALDEHYDE may discolor on exposure to air. Pentanedial polymerizes on heating. Pentanedial is incompatible with strong oxidizing agents. Pentanedial polymerizes in the presence of water.

Health Hazard

Glutaraldehyde is a strong irritant to the nose,eyes, and skin. In rabbits, 250 μg and 500 mg in 24 hours produced severe irritation in theeyes and skin, respectively. The corrosiveeffect on human skin of 6 mg over 3 dayswas severe. However, the acute toxicity ofglutaraldehyde by the oral and dermal routesis low to mild. Ohsumi and Kuroki (1988)determined that the symptoms of acute toxicityof this compound were less severethan those of formaldehyde. But the restraintof growth was more pronounced in micetreated with glutaraldehyde. An oral LD50value of 1300 mg/kg was reported for mice.Inhalation of this compound can cause upperrespiratory tract irritation, headache, and nervousness.Mice exposed at 33 ppm showedsymptoms of hepatitis.

Fire Hazard

Literature sources indicate that Pentanedial is nonflammable.

Flammability and Explosibility

Non flammable

Contact allergens

Glutaraldehyde is a well-know sensitizer in cleaners and health workers. It can also be found in X-ray developers or in cosmetics.

Biochem/physiol Actions

Glutaraldehyde is an effective protein crosslinker and finds application in techniques like enzyme immobilisation microscopy, histochemistry and cytochemistry. It exists in different forms under acidic or neutral conditions. It is a biocide widely used as a disinfectant in hospitals and industries and is toxic to aquatic organisms. Its allergic nature leads to hypersensitivity reactions. Contact of glutaraldehyde vapors in endoscopy contributes to Colitis.

Safety Profile

Poison by ingestion, intravenous, and intraperitoneal routes. Moderately toxic by inhalation, skin contact, and subcutaneous routes. Experimental teratogenic and reproductive effects. A severe eye and human skin irritant. Mutation data reported. When heated to decomp osition it emits acrid smoke and irritating fumes. See also ALDEHYDES.

Potential Exposure

Glutaraldehyde is used in leather tanning; in embalming fluids; as a germicide; as a cross-linking agent for protein and polyhydroxy materi als; as a fixative for tissues; and as an intermediate. Buffered solutions are used as antimicrobial agents in hospitals.

Shipping

UN2810 Toxic liquids, organic, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required.

Purification Methods

Likely impurities are oxidation products-acids, semialdehydes and polymers. It can be purified by repeated washing with activated charcoal (Norit) followed by vacuum filtration, using 15-20g charcoal/100mL of glutaraldehyde solution. Distil it at 60-65o/15mm, discarding the first 5-10%, then dilute with an equal volume of freshly distilled water at 70-75o, using magnetic stirring under nitrogen. The solution is stored at low temperature (3-4o), in a tightly stoppered container, and protected from light. Standardise by titration with hydroxylamine. [Anderson J Histochem Cytochem 15 652 1967, Beilstein 1 IV 3659.]

Incompatibilities

Water contact forms a polymer solution. A strong reducing agent. Incompatible with strong acids; caustics, ammonia, amines, and strong oxidizers. Note: Alkaline solutions of glutaraldehyde (i.e., activated glutar aldehyde) react with alcohol, ketones, amines, hydrazines, and proteins.

Waste Disposal

Dissolve or mix the material with a combustible solvent and burn in a chemical incinera tor equipped with an afterburner and scrubber. All federal, state, and local environmental regulations must be observed.

285-67-6
111-30-8
Synthesis of Glutaric Dialdehyde from Cyclopentene oxide
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