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ACETIC ACID

Background and overview Pharmacological effects Synthetic route Indications Specification Dosage Adverse reactions Precautions Taboo Solidifying fixatives
ACETIC ACID
ACETIC ACID
CAS No.
55896-93-0
Chemical Name:
ACETIC ACID
Synonyms
C2;FEMA 2006;ACETIC ACID;ACITIC ACID;VINEGAR ACID;ETHYLIC ACID;ACETIC ACIDE;ACETIC ACID R;ETHANOIC ACID;ETHANOLIC ACID
CBNumber:
CB2341909
Molecular Formula:
C4H7ClO4S
Formula Weight:
186.61
MOL File:
55896-93-0.mol

ACETIC ACID Properties

Melting point:
16.2 °C(lit.)
Boiling point:
117-118 °C(lit.)
Density 
1.049 g/mL at 25 °C(lit.)
vapor density 
2.07 (vs air)
vapor pressure 
11.4 mm Hg ( 20 °C)
refractive index 
n20/D 1.371(lit.)
Flash point:
104 °F
storage temp. 
-196°C
pka
4.76(at 25℃)
form 
Liquid
color 
Colorless
Relative polarity
0.648
CAS DataBase Reference
55896-93-0(CAS DataBase Reference)

SAFETY

Hazard Codes  C,Xi
Risk Statements  34-41
Safety Statements  23-26-45-39
RIDADR  UN 2790 8/PG 2
WGK Germany  1
RTECS  AF1225000
HazardClass  8
PackingGroup  III

ACETIC ACID price More Price(3)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Alfa Aesar 35567 Acetic acid, 0.1N Standardized Solution 1L $12.7 2017-11-08 Buy
Alfa Aesar 35567 Acetic acid, 0.1N Standardized Solution 4L $42.4 2017-11-08 Buy
Alfa Aesar 35567 Acetic acid, 0.1N Standardized Solution 20L $102 2017-11-08 Buy

ACETIC ACID Chemical Properties,Uses,Production

Background and overview

An important chemical product. Colorless; irritating odor and sour corrosive liquids. More than 1000 BC, humans had begun to use acetate bacteria for wine fermentation to make vinegar. Vinegar has a acetic acid content of 2% to 12%. In 1911, Germany used acetaldehyde oxidation method to create the world's first synthetic acetic acid plant. In 1966 Monsanto, the United States developed the methanol low-pressure carbonylation process (built in 1970), which has become the main method of synthesizing acetic acid, accounting for more than 50% of the total output. In 1999, the world's acetic acid production was about 5 million tons. China began producing acetic acid in the 1950s, producing about 60,000 tons in the 1960s and increasing to 861,300 tons in 2001. The vast majority of acetic acid has been converted into derivatives for application. 40% to 50% has been used for the production of vinyl acetate in China and the United States. Both acetate ester and cellulose acetate accounts for 10% to 12%; solvent application accounts for 20% to 25%.

Pharmacological effects

This product has anti-bacterial and fungal infections. 5% solution has a bactericidal effect on Haemophilus and Pseudomonas. 0.5% ~ 2% solution has antiseptic effect on lavage wound sterilization; different concentrations of acetate can be used to treat various skin shallow fungal infections; the product has bactericidal efficacy.

Synthetic route


Alcohol oxidation: 95% of the raw alcohol and 76% of the alcohol recovered in the workshop are mixed in the mixing tank ratio into 84 ± 0.5% dilute alcohol, the alcohol ingredient is heated by evaporation pot into the oxidation furnace, and has reaction to generate acetaldehyde gas at 555 ± 5 ℃ high temperature and under the catalysis of electrolytic silver. The reaction gas mixture enters into the absorption tower after being condensed, and is diluted with about 8-10% of dilute acetaldehyde after being absorbed by water once. Acetaldehyde refining and alcohol recovery: dilute acetaldehyde is sent into the acetaldehyde distillation column for pressure distillation; control the top temperature at 45 ± 2 ℃ and pressure at 0.15Mpa; the tower gives pure acetaldehyde. Bottoms temperature should be controlled at 121 ± 3 ° C, the material is pressurized into the alcohol recovery column distillation with the tower temperature being controlled at 90 ± 5 ° C; the tower top finally produce about 76% alcohol to be used as the ingredient of the alcohol oxidation process; control the bottoms temperature at 110 ± 3 ℃, and the waste water is discharged through the tower kettle.
Acetaldehyde oxidation: Acetaldehyde enters into the oxidation tower through the action of the pressure pump; it has reaction with the compressed air at a temperature of 50 ~ 80 ℃, pressure 0.20 ~ 0.22Mpa and under a certain amount of manganese acetate to generate crude acetic acid. The crude acetic acid is discharged from the upper discharge port of the oxidation tower to the crude acetic acid storage tank; the unreacted acetaldehyde is condensed and separated from the top of the tower through the condenser, the liquid is refluxed to the bottom of the oxidation tower, and the exhaust gas is further absorbed into the rear of the oxidation tower by the bubbling absorber into the atmosphere.
Acetic acid refinement: The crude acetic acid is evaporated by the high-boiling pot to separate the manganese acetate from the heavy component, the temperature of the high-boiling evaporation pot is controlled at 120 ± 2 ℃, and the manganese acetate at the bottom of the high-boiling pot is discharged into the manganese circulation tank of the acetaldehyde oxidation process for recycling. The light fraction in the top enters into the concentration distillation column, and the bottoms temperature is controlled at 123 ± 3 ° C; acetic acid inside the tower is continuously and quantitatively discharged into the finished product evaporating pot and further distilled and condensed into acetate at 120 ± 2 ℃ into the finished product metering tank. After qualification, it is sent into the finished product pot. The temperature of the top of the tower is controlled at 100 ± 2 ℃. The dilute acid produced at the top of the tower enters into the measuring tank and is put into the dilute acid tank after measurement.

Production route includes BP Cativa process and Celaness AOPlus process.
BP Cativa process
BP is the world's largest provider of acetic acid, and 70% of the world's acetic acid production uses BP technology. BP introduced the Cativa technology patent in 1996. The Cativa process uses a new iridium-based catalyst system and uses a variety of new additives such as rhenium, ruthenium and osmium. The iridium catalyst system has higher activity than rhodium catalysts with few by-products and operates at lower water concentrations (less than 5%), which greatly improves traditional methanol carbonylation, cuts production costs by up to 30%, and reduces expansion costs by 50%. In addition, due to the decrease of water concentration, the CO utilization efficiency is increased and the steam consumption is reduced.
Celanese AOPlus process
Celanese is also one of the largest acetic acid producers in the world. In 1978, the Hurst-Celanese Company (now Celanese) commissioned a Monsanto acetic acid plant at Lake Clare in the U.S. state of Texas. In 1980, Celanese Corporation introduced the AOPlus method (acid optimization method) technology patents, greatly improving the Monsanto process. The AOPlus process increases the rhodium catalyst stability by adding high concentrations of inorganic iodine (mainly lithium iodide), and the water concentration in the reactor after the addition of lithium iodide and methyl iodide.

Indications

This product has anti-bacterial and fungal infections. 2% to 5% solution has a bactericidal effect on Haemophilus and Pseudomonas. It also has effect on Candida, Aspergillus and Trichomonas. It also has spermicidal effect. Various concentrations can be used for the treatment of various skins shallow bacterial or fungal infections, but also for vaginal trichomoniasis, burn wound infection, prevention of flu or flu and contraception.

Specification

Acetic acid solution: 0.1% ~ 5% (concentration required).

Dosage

  • Onychomycosis: Cotton ball immersed in 30% glacial acetic acid solution is placed on the sick arm, once daily and once for 10-15 minutes until disease A is removed and the treatment continues for 2 weeks.
  • Hand, foot and ringworm: Submerge feet with 10% glacial acetic acid solution once daily and once for 10 minutes for 10 consecutive days. If not cured, repeat once every other week.
  • Pityriasis: coated with 5% glacial acetic acid solution 2 times a day.
  • Body ringworm: rub with 5% ~ 10% glacial acetic acid solution, 2 times a day.
  • Corn and wart: apply the affected area with 30% glacial acetic acid once daily.
  • Lavage the wound: with 0.5% ~ 2% solution.

Adverse reactions

Can cause contact dermatitis. 30% solution of onychomycosis can cause chemical paronychia. There are also tingling and burning sensations.

Precautions

Avoid contact with eyes; all kinds of shallow skin fungal infections can be treated with different concentrations of this product.
  1. treatment of onychomycosis: after cleaning the lesion, use blunt knife to skive the onychomycosis, be careful not to contact a ditch; can coat a layer of vaseline for protection in nearby skin;
  2. facial ringworm disease should be not treated with this product;
  3. high concentration of acetic acid has a corrosive effect, avoid using it for the treatment of other ringworm except onychomycosis;
  4. treatment of corn; clean the lesions first and immerse in hot water for 15 to 30 minutes; use vaseline to protect nearby normal skin before applying medicine.

Taboo

Allergic patients and patients of otitis media perforation should be disabled.

Solidifying fixatives

Acetic acid is a colorless and transparent liquid, being highly irritating. It is condensed into ice in cold condition, thus being also known as glacial acetic acid. Acetic acid can be formulated into solutions of various ratios using water and alcohol; the concentration ranges from 0.2 to 5%; it is often used together with other fixatives. It has strong penetration capability with single use causing protoplasm expansion, thus often being used in combination with alcohol, formaldehyde. Acetic acid is an excellent fixative of chromosomes, so the fixing solutions of chromosomes almost all contain acetic acid. Features: strong penetration capability; can cause tissue expansion.

ACETIC ACID Preparation Products And Raw materials

Raw materials

Preparation Products


ACETIC ACID Suppliers

Global( 115)Suppliers
Supplier Tel Fax Email Country ProdList Advantage
Henan Tianfu Chemical Co.,Ltd.
0371-55170693
0371-55170693 info@tianfuchem.com CHINA 20810 55
3B Pharmachem (Wuhan) International Co.,Ltd. 86-21-50328103 * 801、802、803、804 Mobile:18930552037
86-21-50328109 3bsc@sina.com China 15940 69
Alfa Aesar 400-610-6006; 021-67582000
021-67582001/03/05 saleschina@alfa-asia.com China 30309 84
Beijing Ouhe Technology Co., Ltd +86-10-4006331231;+86-10-51280831;+86-10-82967028
+86-10-82967029 sales@ouhechem.com China 10816 60
Accela ChemBio Co.,Ltd. 400-066-5055
021-50795055 sales@accelachem.com China 10584 64
Syntechem Co.,Ltd Please Email
E-Mail Inquiry info@syntechem.com China 13094 57
Shanghai Sunway Pharmaceutical Technology Co., Ltd +86 (21) 51613915
+86 (21) 51613951 sales@sunwaypharm.com China 9917 57
Chengdu Forest Science and Technology Development Co., Ltd. +86 (28) 87925786
+86 (28) 61777050 sales@cdforestchem.com China 2000 58
9ding chemical ( Shanghai) Limited 4009209199
86-021-52271987 sales@9dingchem.com China 18260 56
Chuzhou DeWei Chemical Technology Co., Ltd. 0550-3593607
0550-3160922 deweichem@126.com China 6679 56

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