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Triamcinolone acetonide

CAS No.
76-25-5
Chemical Name:
Triamcinolone acetonide
Synonyms
TRIAMCINOLONE ACETONIDE ACETATE;Triam;Refrigerator;KENALOG;Trymex;ERIC-1;Triacet;Azmacort;Nasacort;Aristogel
CBNumber:
CB4186553
Molecular Formula:
C24H31FO6
Molecular Weight:
434.5
MDL Number:
MFCD00056834
MOL File:
76-25-5.mol
MSDS File:
SDS
Last updated:2024-03-29 18:52:01

Triamcinolone acetonide Properties

Melting point 274-278°C (dec.)
alpha D23 +109° (c = 0.75 in chloroform)
Boiling point 576.9±50.0 °C(Predicted)
Density 1.1517 (estimate)
refractive index 1.5980 (estimate)
storage temp. Refrigerator
solubility Practically insoluble in water, sparingly soluble in ethanol (96 per cent).
pka 12.87±0.10(Predicted)
color White to Off-White
Water Solubility Soluble in DMSO or ethanol. Slightly soluble in water.
Merck 9596
BCS Class 4
Stability Combustible. Incompatible with strong oxidizing agents.
InChIKey YNDXUCZADRHECN-JNQJZLCISA-N
FDA UNII F446C597KA
NCI Drug Dictionary Aristocort
NIST Chemistry Reference Triamcinolone acetonide(76-25-5)
EPA Substance Registry System Triamcinolone acetonide (76-25-5)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS07,GHS08
Signal word  Danger
Hazard statements  H302-H360
Precautionary statements  P201-P202-P264-P270-P301+P312-P308+P313
Hazard Codes  T
Risk Statements  61
Safety Statements  53-45
WGK Germany  3
RTECS  TU3920000
TSCA  Yes
HS Code  29372290
Toxicity LD50 oral in mouse: 5gm/kg
NFPA 704
0
2 0

Triamcinolone acetonide price More Price(42)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich PHR1701 Triamcinolone acetonide Pharmaceutical Secondary Standard; Certified Reference Material 76-25-5 1g $173 2024-03-01 Buy
Sigma-Aldrich 1677002 Triamcinolone acetonide United States Pharmacopeia (USP) Reference Standard 76-25-5 500mg $436 2024-03-01 Buy
Sigma-Aldrich BP339 Triamcinolone acetonide British Pharmacopoeia (BP) Reference Standard 76-25-5 50MG $271 2023-06-20 Buy
Alfa Aesar J63548 Triamcinolone acetonide, 98+% 76-25-5 1g $134 2024-03-01 Buy
Alfa Aesar J63548 Triamcinolone acetonide 98+% 76-25-5 250mg $50.3 2023-06-20 Buy
Product number Packaging Price Buy
PHR1701 1g $173 Buy
1677002 500mg $436 Buy
BP339 50MG $271 Buy
J63548 1g $134 Buy
J63548 250mg $50.3 Buy

Triamcinolone acetonide Chemical Properties,Uses,Production

Appearance and properties

Triamcinolone acetonide, its acetate form appears to be white or white-like crystalline powder. The drug is odorless, with bitter taste. It is hardly soluble in water, slightly soluble in ethanol, soluble in chloroform, and slightly soluble in acetone.

Glucocorticoid drugs

Triamcinolone acetonide is a kind of long-term glucocorticoid drugs which is now widely used in clinical Dermatology of China. It belongs to adrenocorticotropic hormone drugs. It is the derivative of Triamcinolone, and with the same function as Triamcinolone. Triamcinolone acetonide functions in anti-inflammatory, anti-allergic, anti-itching and shrinking capillaries. What’s more, besides its weak water-sodium retention, the effect of Triamcinolone acetonide for anti-inflammatory, anti-allergic is much stronger and more durable than hydrocortisone (10 to 30 folds), and prednisone. It can also treat bronchial asthma by aerosol inhalation with very strong and durable effect. Triamcinolone acetonide has better efficacy on local treatment compared with triamcinolone. It is Oral absorbed easily. Taking orally 5mg of the drug yields a bioavailability of about 23%. Its plasma concentration reaches peak (105 ng/mL) within one hour with the half-life is being 2 hours; It has a slow intramuscular absorption rate which takes effect within hours, and gives maximal effect within 1 to 2 days. The effect can be maintained for 2~3 weeks; the absorption rate of intradermal and intra-articular injection of the drug is low, but has a long-lasting effect; generally the efficacy can be maintained for more than 1-2 week per injection. This product has a low binding rate with plasma albumin protein, and is metabolized into non-active product in the liver, kidneys and tissues which is then further excreted by the kidneys. It also has a long-lasting effect upon local injection. Moreover, topical ointments can also produce a good effect. Clinically triamcinolone acetonide is used for treatment of various skin diseases such as atopic dermatitis, contact dermatitis, seborrheic dermatitis, neurodermatitis, eczema, psoriasis, psoriasis, lichen planus and skin pruritus, as well as bronchial asthma, rheumatoid arthritis, acute sprains, chronic ache in back and legs, frozen shoulder, tenosynovitis, ophthalmic inflammation, oral mucosal congestion, erosion, ulcers, granulomatous cheilitis, and oral mucosa chronic infectious diseases, Furthermore, it can also be used for local injection treatment in keloid, cystic acne, discoid lupus erythematosus, alopecia areata and other small area of damages. Triamcinolone acetonide nasal spray can be used for the prevention and treatment of perennial, seasonal allergic rhinitis, and vasomotor rhinitis. Intra-articular injection of this drug can eliminate inflammation and pain, swelling or can alleviate, pain, stiffness and swelling feeling.
The above information is edited by the Chemicalbook of Dai Xiongfeng.

Uses

Triamcinolone acetonide is a topical and systemic corticosteroid belonging to the group B (triamcinolone acetonide) type of steroids. Triamcinolone acetonide is an adrenal cortex hormone drug. As an antiasthmatic (inhalant) and antiallergic (nasal), it could used for treating diseases such as neurodermatitis, eczema, psoriasis, joint pain, and asthma.

Category

Toxic Substances.

Toxicity grading

Highly toxic.

Acute toxicity

Subcutaneous-rat LD50: 13.1 mg/kg; intraperitoneal-Mouse LD50: 105 mg/kg.

Flammability hazard characteristics

Combustible; combustion produces toxic fumes of fluoride.

Storage Characteristics

Treasury: ventilation, low-temperature and dry; store separately from food raw materials.

Extinguishing agent

Dry powder, foam, sand, carbon dioxide, water spray.

Description

Triamcinolone acetonide is a synthetic corticosteroid. It decreases cytokine levels, the firing rate of sensory neurons, and mechanical hypersensitivity in a rat spinal nerve ligation model when used at a dose of 1.5 mg/kg prior to and following surgery for three days. Triamcinolone acetonide also decreases outflow facility in a mouse model of steroid-induced glaucoma when 20 μl of a 40 mg/ml suspension is administered subconjunctivally. Formulations containing triamcinolone acetonide are used in the treatment of diabetic macular edema.

Chemical Properties

White Solid

Originator

Kenalog,Squibb,US,1958

Indications

Triamcinolone acetonide (Aristocort, Kenalog) is a synthetic fluorinated corticosteroid.

Definition

ChEBI: A synthetic glucocorticoid that is the 16,17-acetonide of triamcinolone. Used to treat various skin infections.

Manufacturing Process

A solution of 250 mg of 9α-fluoro-11β,16α,17α,21-tetrahydroxy-1,4- pregnadiene-3,20-dione in 70 ml of hot acetone and 7 drops of concentrated hydrochloric acid is boiled for 3 minutes. After standing at room temperature for 17 hours, the reaction mixture is poured into dilute sodium bicarbonate and extracted with ethyl acetate. The extract is washed with saturated saline solution, dried and evaporated to a colorless glass. The residue is crystallized from acetone-petroleum ether to afford 166 mg of the acetonide, MP 270° to 274°C, decomposition, (with previous softening and browning). Three recrystallizations from acetone-petroleum ether give 113 mg of 9α-fluoro- 11β,21-dihydroxy-16α,17α-isopropylidenedioxy-1,4-pregnadiene-3,20-dione, MP 274° to 279°C, decomposition, (with previous softening and browning).

brand name

Triamcinolone acetonide was sold under the brand name Kenalog among others.

Therapeutic Function

Glucocorticoid

General Description

Triamcinolone acetonide is approximately 8 times morepotent than prednisone in animal inflammation models.Topically applied triamcinolone acetonide is a potent antiinflammatoryagent, about 10 times more sothan triamcinolone. The plasma half-life is approximately 90minutes, although the plasma half-life and biological halflivesfor GCs do not correlate well. The hexacetonide isslowly converted to the acetonide in vivo and is given onlyby intra-articular injection. Only triamcinolone and the diacetateare given orally. The acetonide and diacetate may begiven by intra-articular or intrasynovial injection. In addition,the acetonide may be given by intrabursal or, sometimes,IM or subcutaneous injection. A single IM dose of thediacetate or acetonide may last up to 3 or 4 weeks. Plasmalevels with IM doses of the acetonide are significantly higherthan with triamcinolone itself. The acetonide is also used totreat asthma and allergic rhinitis.

General Description

The three main metabolitesof triamcinolone acetonide (Azmacort, Nasacort) are 6β-hydroxytriamcinolone acetonide, 21-carboxytriamcinoloneacetonide, and 6β-hydroxy-21-carboxytriamcinolone acetonide.All are much less active than the parent compound.The 6β-hydroxyl group and the 21-carboxy group are bothstructural features that greatly reduce GC action. The increasedwater solubility of these metabolites also facilitatesmore rapid excretion.

Clinical Use

Triamcinolone acetonide used topically to treat various skin conditions, to relieve the discomfort of mouth sores, and by injection into joints to treat various joint conditions.Triamcinolone acetonide frequently is used by inhalation for the treatment of lung diseases (e.g., asthma).

Side effects

The side effects of using Triamcinolone acetonide include:Skin dryness, flaking, crusting, burning, or blistering; Skin irritation; Skin soreness, itching, swelling, scaling, or severe redness; Scaling or redness near mouth; Skin thinning or bruising, especially in skin folds (like between the finger) or on the face (when directed to use it there); New or worsening pimples or acne; Skin burning and itching with tiny red blisters; Skin softening; Itching, pain, or burning sensation in hairy areas, or pus at the root of the hair; Increased hair growth on the legs, arms, back, or forehead; Lightening of skin tone; Red or purple lines on the arms, face, legs, groin, or trunk.

Safety Profile

Poison by subcutaneous and intraperitoneal routes. An experimental teratogen. Other experimental reproductive effects. Human mutation data reported. When heated to decomposition it emits acrid smoke and toxic fumes of F-.

Veterinary Drugs and Treatments

The systemic veterinary labeled product (Vetalog? Injection) is labeled as “indicated for the treatment of inflammation and related disorders in dogs, cats, and horses. It is also indicated for use in dogs and cats for the management and treatment of acute arthritis, allergic and dermatologic disorders.”
Glucocorticoids have been used in an attempt to treat practically every malady that afflicts man or animal, but there are three broad uses and dosage ranges for use of these agents. 1) Replacement of glucocorticoid activity in patients with adrenal insufficiency, 2) as an antiinflammatory agent, and 3) as an immunosuppressive. Among some of the uses for glucocorticoids include treatment of: endocrine conditions (e.g., adrenal insufficiency), rheumatic diseases (e.g., rheumatoid arthritis), collagen diseases (e.g., systemic lupus), allergic states, respiratory diseases (e.g., asthma), dermatologic diseases (e.g., pemphigus, allergic dermatoses), hematologic disorders (e.g., thrombocytopenias, autoimmune hemolytic anemias), neoplasias, nervous system disorders (increased CSF pressure), GI diseases (e.g., ulcerative colitis exacerbations), and renal diseases (e.g., nephrotic syndrome). Some glucocorticoids are used topically in the eye and skin for various conditions or are injected intra-articularly or intra-lesionally. The above listing is certainly not complete.

Metabolism

Triamcinolone acetonide frequently is used by inhalation for the treatment of lung diseases (e.g., asthma). After inhalation, triamcinolone acetonide can become systemically available when the inhaled formulation is swallowed and absorbed unchanged from the GI tract, causing undesirable systemic effects. Triamcinolone acetonide that is swallowed is metabolized to 6β-hydroxytriamcinolone acetonide, 21-carboxytriamcinolone acetonide, and 21-carboxy-6β-hydroxytriamcinolone acetonide, all of which are more hydrophilic than their parent drug. Only approximately 1% of the dose was recovered from the urine as triamcinolone acetonide. Triamcinolone is not a major metabolite of triamcinolone acetonide in humans, suggesting that acetonide is resistant to hydrolytic cleavage. Triamcinolone acetonide is approximately eight times more potent than prednisolone.

124-94-7
67-64-1
76-25-5
Synthesis of Triamcinolone acetonide from Triamcinolone and Acetone
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View Lastest Price from Triamcinolone acetonide manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Triamcinolone acetonide pictures 2024-04-25 Triamcinolone acetonide
76-25-5
US $0.00-0.00 / g 1g 99% 100kg Wuhan Cell Pharmaceutical Co., Ltd
Triamcinolone acetonide pictures 2024-04-22 Triamcinolone acetonide
76-25-5
US $150.00-45.00 / Kg/Bag 1Kg/Bag 0.99 20 tons Sinoway Industrial co., ltd.
Triamcinolone acetonide pictures 2024-03-29 Triamcinolone acetonide
76-25-5
US $0.00 / kg 1kg 99% 20tons Shaanxi TNJONE Pharmaceutical Co., Ltd
ARISTODERM 9ALPHA-FLUORO-11BETA,21-DIHYDROXY-16ALPHA,17-ISOPROPYLIDENEDIOXY-1,4-PREGNADIENE-3,20-DIONE 9ALPHA-FLUORO-16ALPHA-HYDROXYPREDNISOLONE 16ALPHA,17ALPHA-ACETONIDE 9ALPHA-FLUORO-11BETA,16ALPHA,17ALPHA,21-TETRAHYDROXY-1,4-PREGNADIENE-3,20-DIONE 16,17-ACETONIDE 9a-fluoro-11b,16a,17a,21-tetrahydroxy-1,4-pregnadiene-3,20-dione 16,17-acetonide 9a-fluoro-16a-hydroxyprednisolone 16a,17a-acetonide ALPHA-FLUORO-11BETA,16ALPHA,17,21-TETRA-HYDROXYPREGNA-1,4-DIENE-3,20-DIONE 1,4-PREGNADIEN-9-ALPHA-FLUORO-11-BETA, 16-ALPHA, 17,21-TETROL-3,20-DIONE-16,17-ACETONIDE 1,4-PREGNADIEN-9ALPHA-FLUORO-11BETA,16ALPHA,17ALPHA,21-TETROL 3,20-DIONE 16,17-ACETONIDE (11beta,16alpha)-9-Fluoro-11,21-dihydroxy-16,17-[(1-methylethylidene)bis(oxy)]pregna-1,4-diene-3,20-dione (11beta,16alpha)-e)bis(oxy)] 4b-Fluoro-6b-glycoloyl-5-hydroxy-4a,6a,8,8-tetramethyl-4a,4b,5,6,6a,6b,9a,10,10a,10b,11,12-dodecahydro-2H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-2-one 9-alpha-fluoro-11-beta,21-dihydroxy-16-alpha-isopropylidenedioxy-1,4-pregnad 9-alpha-fluoro-16-alpha-17-alpha-isopropyledenedioxyprednisolone 9alpha-Fluoro-16alpha-17alpha-isopropyledenedioxyprednisolone 9alpha-Fluoro-16alpha-17alpha-isopropylidenedioxy-delta -1-hydrocortisone 9-alpha-fluoro-16-alpha-17-alpha-isopropylidenedioxy-delta-1-hydrocortisone 9alpha-Fluoro-16-hydroxyprednisolone acetonide 9-alpha-fluoro-16-hydroxyprednisoloneacetonide Acetospan Adcortyl Adcortyl A Aristocort A Aristocort acetonide aristocortacetonide component of Mycolog ii component of Myco-triacet ii component of Mytrex component of Panolog Coupe-A Delphicort triamsinoloneacetonide Vetalog triamcinolone16,17-acetonide Triam-Injekt Triamonide 40 Triamsinolone acetonide TRIAMCINOLONE ACETONIDE TRICINOLON Adcortyl, Azmacort, Delphicort, Extracort, Ftorocort, Kenacort-A, Tramacin, Triam, Tricinolon, Vetalog, Volon A, Volonimat, Pregna-1,4-diene-3,20-dione, 9-fluoro-11,21-dihydroxy-16,17-(1-methylethylidene)bis(oxy)-, (11.beta.,16.alpha.)- Volon A Volon A 40 Volonimat RINETON 16alpha-Hydroxy-9alpha-fluoroprednisolone acetonide Triamcinolone acetonide,>=99% Triamcinoione acetonide Triamcinolone Acetonide (500 mg) (11β,16α)-9-Fluoro-11,21-dihydroxy-16,17-[(1-Methylethylidene)bis(oxy)]-pregna-1,4-diene-3,20-dione 9α-Fluoro-16α-hydroxyprednisolone 16α,17α-acetonide TriaMcinolon Acetonide TriaMcinolon-6-d1 Acetonide-d6 TriaMcinolone Acetonide USP TriaMcinolone acetonid Triamcinolone acetonide Solution, 100ppm Triamcinolone acetonide for system suitability Anti-TACC3, C-Terminal antibody produced in rabbit