3,5 – Xylenol

Chinese name: 3,5 – dimethylphenol
Chinese alias : 3,5 – xylenol ; MX; 3,5 – xylenol ; 1 – hydroxy-3 ,5 – dimethylbenzene ; 1,3,5 – xylenol ; 1,3 – xylene -5 – phenol ; 1,3 – dimethyl-5 – hydroxy ; 3,5 – xylene -1 – phenol
English name : 3,5-Dimethylphenol
English Name : 3,5-Xylenol; OBPA; MX
CAS No:. 108-68-9
EINECS: 203-606-5
Molecular formula : C8H10O
Molecular Weight: 122.17
Melting point : 63-66 ℃
Boiling point : 222 ℃
Refractive index : 1.5362 (20 C)
Flash Point : 109 ℃
Inchi: InChI = 1/C8H10O/c1-6-3-7 (2) 5-8 (9) 4-6/h3-5, 9H ,1-2H3
Density: 0.968
Water Solubility : 5.3 g / L (25 ℃)
Risk Codes : R24/25, R34,
RIDADR : UN 2261
Safety Description : S26, S28A, S36/37/39, S45,
HS CODE: 29071400
Packing Group : II
Hazard Class: 6.1
Storage temperature :. Store in a tightly closed container Store in a cool, dry, well-ventilated area away from incompatible substances.
Acute toxicity : Oral – Rat LD50: 608 mg / kg ; Oral – mouse LD50: 477 mg / kg
Extinguishing Media : Carbon dioxide , sand , foam , dry powder
Fire hazard : Flash point data for 3,5-Dimethylphenol are not available 3,5-Dimethylphenol is probably combustible..
Toxicity grading : highly toxic
Stimulus data: Eyes – 0.25 mg rabbit severe
Explosive hazardous characteristics : high fever case , the fire or contact with oxidants, cause a fire danger. Corrosive.
Storage features: Treasury ventilation low-temperature drying ; and food materials , bases , oxidizers separate storage
Flammable hazardous characteristics : flammable ; combustion releases toxic chlorine fumes

Buluoboer

Characters (Characteristics):
English name : Bronopol; Biocide
English Name : Bronopol; 2-Bromo-2-nitropropane-1 ,3-diol; 1,3-Propanediol, 2-bromo-2-nitro-; 2-Bromo-1-nitro-1 ,3-propanediol; 2 – bromo-2-nitro-3-propanediol; 2-Bromo-2-nitropropan-1 ,3-diol; 2-Nitro-2-bromo-1 ,3-propanediol; 3-Propanediol ,2-bromo-2-nitro- 1; beta-Bromo-beta-nitrotrimethyleneglycol; Bioban BNPD-40
Chemical Name : 2 – bromo-2 – nitro -1 ,3 – propanediol
Chinese alias : 2 – bromo-2 – nitro-1 ,3 – propanediol ; bronopol ; bronopol WP ; bromopropanol ; bromine nitrate propanol ; 2 – nitro -2-1,3 – propanediol ( Broken Ball ) ; 2 – bromo -2 – nitro-1 ,3 – propanediol ( Buluoboer ) ; bronopol ; Buloh Boer ; leather Le Bao ; 2 – bromo -2 – nitro – 1,3 – propanol ; 2 – bromo -2 – nitro -1 ,3 – diol
CAS NO. :52-51-7
Formula : C3H6BrNO4
Molecular Weight : 199.98
Quality standards:
Appearance: odorless or smell slightly bromine , white or light yellow crystalline powder.
Content : ≥ 99%
Melting point (MP) :121-129 ℃
Moisture : ≤ 0.5%
The remaining indicators in line with the standard version of the British Pharmacopoeia BP98
Solubility: soluble in water ( 25 weight / volume / 25 ℃) and polar organic solvents. Low solubility in oil , 23 ℃ , only to dissolve 0.5g, oil / water partition coefficient.
Safety performance:
Acute toxicity : LD50 is 222mg/Kg weight ( female oral ) -266mg/kg weight ( male oral ) , male and female mice were no significant differences in toxicity tests . Consistent with the foreign literature reports . Moderate level of toxicity in the toxicity .
To the skin and mucous membranes Test : When the concentration is less than 0.5% Bronopol concentration on the skin and mucous membranes without any stimulation . When Buluoboer 0.5% dilution ( 10-fold higher concentration ) , a one-time rabbit skin irritation test , the result is a light irritation.
Skin allergy test : When Buluoboer concentration of less than 0.25% , no contact allergy.
Buluoboer inhibitory spectrum
When the presence of organic cosmetics , non-ionic , nonionic surfactants yin and yang , did not affect the inhibitory effect Buluoboer , nor antagonism to each other. Protein content in the formulation is less than 10% , the excellent effect can Bronopol corrosion.
And amount of use of
Broken Ball can be used in creams, lotions, shampoos and other products. General dosage 0.02-0.05 % in cosmetic products , the maximum allowable dosage of 0.1% , no residual emissions will not cause accumulation of pollution .
Application PH value range :4 -10
Usage: biocides , sterilization is mainly used for industrial water recycling, pulp and paper , paints, plastics , cosmetics, timber, cooling water systems, and industrial uses, mildew , corrosion , algae and so on. Under alkaline conditions , it is easy to lose activity. The most suitable range of Ph 4-6
Quality indicators
(Quality Specification): 99%
Packing & Storage
(Package & Storage): Packaging: 25

soda ash production methods

Development History
4.1.1 soda ash Laboratory Methods
Laboratory Preparation of sodium carbonate :
.
4.1.2 soda ash Lv Bulan Law
First in 1791 , the ancients began with salt , sulfuric acid, coal, limestone as raw material to produce sodium carbonate , is Lv Bulan method.
This method does not fully utilize the raw material , poor working conditions, poor product quality , and gradually replaced by Solvay process .
4.1.3 soda ash Solvay process
1859 , Belgian Solvay , with salt , ammonia , carbon dioxide as raw materials, at room temperature to precipitate sodium bicarbonate from the solution, heating it, and that the decomposition of sodium carbonate , alkali people this method is known as the Soxhlet this method has been in use ever since.
4.1.4 soda ash Houde Bang Law
1943 Chinese people studying abroad returned Houde Bang , he combined Mainland China ‘s national conditions and lack of salt on the Solvay process improvements , the two industrial joint soda ash and ammonia , while the production of sodium carbonate and ammonium chloride fertilizer , greatly improved salt utilization, is Hou soda method.
Reaction principle
Soxhlet soda method and the main chemical reaction Hou soda method are :
Reaction one :
NaHCO3 ( sodium bicarbonate ) soluble only under these conditions , greater than the solubility of sodium bicarbonate dissolved under this condition , the precipitated solid sodium bicarbonate , filtered to afford solid sodium bicarbonate .
Reaction II:
Hou alkali and alkali Soxhlet method different method is the preparation of the Soxhlet process is recycled NH3 :
And Hou law throughout the preparation process , NH4Cl directly as a byproduct of soda ash —- fertilizer.
So Soxhlet products are sodium carbonate, calcium chloride byproduct ; while Hou law product is sodium carbonate, ammonium chloride byproduct .
Hou alkali method
Namely:
① NaCl ( saturated ) + NH3 + H2O + CO2 ==== NH4Cl + NaHCO3

Ammonia and carbon dioxide reacts with the water molecule of ammonium bicarbonate , which is the first step .
( 1 )
The second step : the reaction of sodium bicarbonate and precipitates of sodium bicarbonate and ammonium chloride , sodium bicarbonate and the reason is because precipitation of the less soluble .
(2) NH ₄ HCO ₃ + NaCl ( saturated ) ==== NH ₄ Cl + NaHCO ₃ ↓
Part can be directly synthesized sodium bicarbonate factory sales , and the rest will be thermal decomposition of sodium bicarbonate to produce sodium carbonate, carbon dioxide can be generated back to the first step !
( 3 )
According NH4Cl solubility than NaCl, at a low temperature than the solubility of NaCl principle , 278K ~ 283K (5 ℃ ~ 10 ℃) when , salt powder was added to the mother liquor , leaving to crystallize for doing NH4Cl nitrogen alone .
Advantages of this method : the ammonia soda process retains the advantages , it eliminates the drawbacks that increase the utilization of salt to 96%; NH4Cl do nitrogen ; ammonia plant with a joint , so that the ammonia feed gas CO into CO2, leather In addition to this process CO2 CaCO3 system .

The biological process of poly glutamic acid was published in Jiangsu

Since the 90s of the last century, development green chemical products has become a trend in the development of chemical industry, and the polymerization of amino acid series products development also emerged from. In recent years, Japan, the United States and other developed countries have carried out the research of microbial fermentation gamma polyglutamic acid, the Japanese walk in the forefront of the world, which Meiji Seika has realized the gamma poly glutamic acid in commercial production, and gradually extended its application, and the gamma poly glutamic acid also has been rarely reported.
Gamma polyglutamic acid (PGA) is a by microbial synthesis of poly amino acids, has excellent biological compatibility and biodegradability, the in vivo degradation for glutamic acid directly absorbed and used as biomedical materials. In addition, because of strong water absorption of poly glutamic acid, easy modification, can be rapidly degraded in nature, will not cause environmental pollution, can be used in cosmetics, food and drug delivery.
The topic group for the production of poly glutamic acid is mostly used in Japan, the extraction process is very complex, the production cost is very high. Through natural selection and mutation, strains with independent intellectual property rights, combined with the optimization of the enzyme production mechanism and fermentation conditions, gamma poly glutamic acid concentration of generated 30 grams / liter above, the glutamate substrate conversion rate of 80% of the production level and production rate reached 25 grams / liter / hour. At the same time, the new technology will be used to separate the traditional means of separation and ultrafiltration membrane separation means to simplify the process, so that the yield of the product reached 80%, the product content of 99%. The preparation and application of gamma poly glutamic acid high water absorbent resin were studied, and the water absorption of high water absorbent resin with water absorption rate of 1600 g / g was obtained. According to reports, the resin is a kind of sand fixing vegetation eco friendly materials, and is currently the preliminary study on the agricultural application.

The main purpose 8-Hydroxyquinoline

1 ,8-Hydroxyquinoline is widely used for the determination and separation of metals . Precipitating agent and precipitation and separation of metal ions in the extraction agent , with the following metal ions : Cu +2, Be +2, Mg +2, Ca +2, Sr +2, Ba +2,?????? Zn? +2, Cd? +2, Al? +3, Ga? +3, In? +3, Tl? +3, Yt? +3, La +3, Pb? +2, B? +3, Sb ? +3, Cr? +3, MoO? +22, Mn? +2, Fe? +3, Co? +2, Ni? +2, Pd? +2, Ce? +3
1 used as pharmaceutical intermediates , synthetic grams Xie Li Ning , clioquinol , flutter respite sensitive materials , but also dye , pesticide intermediates. The product is a halogenated quinoline class of anti- amoebic drug intermediates , including quinoline iodoform , clioquinol , iodoquinol so on. These drugs inhibit the intestinal commensal bacteria play a role in anti- amoebic of amoebic dysentery effective, no outside influence on intestinal amoeba . Foreign reports this class of drugs can cause subacute optic neuropathy , the drug has been disabled in Japan and the United States , caused by the disease iodoquinol than clioquinol rare. 8 – hydroxy quinoline also dye , pesticide intermediates. Copper sulfate and is an excellent antiseptic , disinfectant and fungicide . The product is a complex indicator for chemical analysis.
2 is used as a complexing agent and an extractant precipitation and separation of metal ions , with Cu +2, Be +2, Mg +2, Ca +2, Sr +2, Ba +2, Zn? +2, Cd + 2, Al +3, Ga +3, In +3, Tl +3, Yt +3, La +3, Pb +2, B +3, Sb? +3, Cr +3, MoO? +22, Mn + 2, Fe +3, Co +2, Ni +2, Pd +2, Ce +3, and other metal ions . Determination of organic trace analysis of nitrogen heterocyclic organic synthesis. Also dyes, pesticides and halogenated quinoline class of anti- amoebic drug intermediates . Copper sulfate and is an excellent preservative.
3 of epoxy adhesive can be added to improve the metal ( especially stainless steel ) adhesive strength and heat aging resistance , the amount is generally 0.5 to 3 parts . Halogenated quinoline class of anti- amebic drugs intermediates, pesticide , dye intermediates. Complexometric titration indicator can be used as fungicides, preservatives and industrial polyester resins, phenolic resins and hydrogen peroxide stabilizers, or chemical analysis.
(4) The product is an intermediate halogenated quinoline drugs , but also dyes, pesticide intermediates. Copper sulfate and is an excellent antiseptic , disinfectant and fungicide . Cosmetics maximum allowable content ( mass fraction ) was 0.3% , sunscreen products and products for children under 3 years of age ( as talcum powder ) is disabled and should indicate on the product label ” disabled children under 3 years of age .” In dealing with bacterial infections and bacterial infections of the skin, eczema , lotion 8 – hydroxy quinoline mass fraction of 0.001% to 0.02%. It is also used as a disinfectant , antiseptic and fungicide , and its strong anti- fungal effect . 8-ydroxyquinoline sulfate used in skin creams and lotions content ( mass fraction ) of 0.05 % to 0.5 %.

Oxalic acid and chemical properties

Oxalic acid at 100 ℃ start sublimation , when rapid sublimation 125 ℃ , 157 ℃ when a large number of sublimation , and begin to decompose.
With a base , may occur esterification, acid halide , an amidation reaction . Reduction reaction can also occur , heat decarboxylation reaction . Anhydrous oxalic acid is hygroscopic . Oxalic acid can dissolve in water to form complexes with many metals .
Acidity
Oxalic acid than acetic acid ( acetic acid ) 10000- X , the acid is an organic acid . Its an ionization constant Ka1 = 5.9 × 10 ^ -2, two ionization constant Ka2 = 6.4 × 10 ^ -5. With continuity acids. Can occur with alkali neutralization, the indicator can change color , can emit carbon dioxide and carbonate role .
For example : H2C2O4 + Na2CO3 == Na2C2O4 + CO2 ↑ + H2O
H2C2O4 + Zn == ZnC2O4 + H2 ↑
Reductive
Oxalate has a strong reduction, and oxidant easily oxidized into carbon dioxide and water [ 1 ] . Can make acidic potassium permanganate (KMnO4) solution fade, and reduced to divalent manganese ions. This reaction is used as a quantitative analysis method for determining the concentration of potassium permanganate . Oxalic acid can also wash away spilled ink on the cloth track .
2KMnO4 +5 H2C2O4 +3 H2SO4 == K2SO4 +2 MnSO4 +10 CO2 ↑ +8 H2O
H2C2O4 + NaClO == NaCl +2 CO2 ↑ + H2O
Instability
Oxalic acid at 189.5 ℃ or in case of concentrated sulfuric acid will decompose to produce carbon dioxide , carbon monoxide and water.
H2C2O4 ==== CO2 ↑ + CO ↑ + H2O
Laboratories can use this reaction to the admission of carbon monoxide gas .
Hydrogen oxalate to carbon dioxide, carbon monoxide, ammonia , and water 200 degrees
Toxicity
Oxalic acid is poisonous. On the skin , mucous membrane irritation and corrosion, easily through the skin , mucous membranes absorb lead poisoning . Air maximum allowable concentration of 1m g/m3.
Esterification
Acetic acid ester with an alcohol can be generated . For example, the reaction of acetic acid with ethanol, ethylene malonate.

Benzalkonium chloride application

Pharmacological effects of Cymbalta cationic surfactant broad-spectrum fungicide , alter the bacterial cytoplasmic membrane permeability , so that the cell cytoplasm
Material extravasation.
Drug interactions with the product soap and other anionic surfactants , citrate , iodide , nitrate , permanganate , salicylates , silver , tartrate and alkaloids incompatibility. Aluminum , cotton dressings, fluorescein sodium , hydrogen peroxide , kaolin , lanolin and some sulfa drugs incompatibility. And some synthetic rubber and plastics ingredients may have incompatibility.
[ Dosing instructions ]
1 . Quaternary ammonium surfactants , its bactericidal medium strength , as a fungicide surgical instruments and items not heat , its efficacy is not clear , so 2010 has been replaced by other low toxicity and more efficient disinfectant , try not used to disinfect these items.
(2) The solution for soft contact lenses can not be agents of extinction mother.

3 aqueous solution of this product may be microbial contamination , to reduce the risk of contamination should be used aseptic or further diluted before use , freshly prepared at the desired concentration and dilution in the process of preservation and to take appropriate measures to prevent the the product may be contaminated .
4 and do not use soap, synthetic detergent , or other salts , avoiding the use of aluminum containers. Metal instrument sterilization needs plus 0.5 % sodium nitrite rust.
5 solution shall be stored in PVC bottles , avoiding its plasticizer contained react , so that efficacy disappeared .
6 should not be used for mirrors , ophthalmic instruments and disinfection of synthetic rubber bladder.
[Usage and dosage]
1 . The skin, mucous membrane disinfection 0.1% solution.
2 wounds disinfected with 0.01 % solution .
3 deep wound lavage with a 0.005% solution .
4 vaginal lavage with a solution of 0.02% to 0.05% .
5 . Bladder and urethra lavage solution of 0.005 % or less .
6 0.0025% to 0.005 % solution of the bladder with fluid retention .
7 sterilization of surgical instruments and save with 0.1 % solution of sodium nitrite can rust .
8 0.005 % to 0.02 % solution of antiseptic drops drug use .
9 Wash hands before surgery with 0.05 % to 0.1 % solution soak for 5 minutes
[Preparation and specifications
1 benzalkonium chloride solution : 5% .
2 benzalkonium bromide solution : 5 %.
Adverse reactions
1 This product is a topical solution concentration generally does not cause skin irritation , but some patients after repeated use of an allergic reaction may occur. When used as a preservative in eye drops , has been reported to cause allergic conjunctivitis , vision loss , etc.
(2) The product has a depolarizing muscle relaxant properties, after taking toxic symptoms include respiratory muscle paralysis caused by breathing difficulties and cyanosis, and even lead to suffocation. Central nervous system depression , hypotension , coma and death may also occur.
Reported benzalkonium chloride can cause allergic conjunctivitis , vision loss, contact dermatitis . Eye drops often benzalkonium bromide ( benzalkonium chloride ) as antibacterial agents . 0.1 % concentration in the cornea causes mild discomfort and for about 2 to 3 hours . Carried out within 90 seconds, slit lamp examination , visible in the corneal epithelium with fine gray clot , 10 minutes gray haze visible inner surface of the cornea , and then the surface conjunctival epithelial desquamation occurs . These surface stimulation and visual impairment in one day disappear . To be sure , the risk of glaucoma, dry eye patients , infection and inflammation of the iris with benzene , such as benzalkonium chloride eye drops too many times , for too long, enough to cause damage. They endothelial damage, and epithelial edema incidence bullous keratopathy high, and because of the seriousness of these diseases may cause harm to ignore some of the other secondary , which for corneal epithelial defects or especially ulcers in patients .
3% solution has also been reported to cause nausea enema minutes , cold sweat , eventually leading to death . Used for vaginal douching , some cases cause of death, cause of death due to respiratory paralysis believed to be caused .
Such as benzalkonium chloride, a suitable amount without any adverse reactions. Is caused by excessive use of tachycardia, palpitations , angina , arrhythmias , headache , nervousness , excitement, anxiety, insomnia, bone road muscle cramps, muscle weakness , tremors , sweating, flushing, heat intolerance , fever , diarrhea, vomiting, weight benzalkonium chloride and other similar alleviate symptoms of hyperthyroidism . When T3 overdose , adverse reactions compared with T4 or benzalkonium chloride powder quickly. Reduction or withdrawal causes all the symptoms disappear. T4 caused by overdose symptoms disappear more slowly. Adverse reactions similar performance with benzalkonium chloride hyperthyroidism , such as increased appetite , nervousness, various types of tachycardia , arrhythmias, and increased basal metabolism and so on. 1986 first reported allergic reactions pure benzalkonium chloride preparations caused benzalkonium chloride dysfunction in patients with fever , abnormal liver function , increased eosinophils , after the general withdrawal symptoms can disappear.
For the youth, who benzalkonium chloride dysfunction , T4 may cause short-term pseudo encephalopathy, if used continuously T4 treatment , even if there is no local neurological defects , both sides will have a headache and papilledema appear. Acute poisoning benzalkonium chloride benzalkonium chloride may cause clinical disease syndrome outbreaks resulting in death, but in general there will be only a temporary overdose symptoms of hyperthyroidism . Pharmacists have been reported due to the amount of T4 as mistakenly g mg dose administered to patients , and a dangerous situation . T4, especially T3, if administered intravenously, the heart is very dangerous, so the next unless edema in patients with myxoid life-threatening , and has a good heart monitor conditions before considering intravenous administration , if these patients while dopamine drugs, more dangerous and should be used with caution .
[ Disabled ] caution

One can certainly suffer from glaucoma, dry eye patients , infection and inflammation of the iris benzalkonium chloride with benzene as the number of drops too much , too long enough to cause damage. They endothelial damage, and epithelial edema incidence bullous keratopathy high, and because of the seriousness of these diseases may lead to neglect of other minor hazards, for corneal epithelial defects or especially ulcers in patients .
2 treatment , misuse of local early use of sodium chloride , magnesium sulfate, soft soap solution antagonistic . Timely adoption of appropriate amount of anti-inflammatory corticosteroids , anti-drug absorption after treatment , can reduce symptoms and shorten the course.
Salt and soap and disinfectant prohibited drugs . Not for cystoscopy, ophthalmic instruments and synthetic rubber products for disinfection.
Three elderly patients sensitive to benzalkonium chloride , more than 60 years of age who require replacement of benzalkonium chloride of about 25% lower than the young .
4 should be used with caution in the following conditions :
① cardiovascular disease, including angina , atherosclerosis , coronary heart disease , hypertension , myocardial infarction patients ;
② for longer duration, severe illness hypothyroidism or myxedema patients using this drug should be careful to start with a small dose , after slowly increasing the dose until the physiological replacement ;
③ associated with pituitary dysfunction , or adrenal insufficiency should be used in patients with corticosteroids, adrenal function returned to normal soon after the use of the drugs. For heart patients and long-term hypothyroidism who use benzalkonium chloride replacement therapy is more dangerous, and adrenal insufficiency often associated with low thyroid function , if benzalkonium chloride alternative treatment prior to corticosteroid therapy , there may be Addison’s crisis.
For patients with swelling of benzalkonium chloride , benzalkonium chloride secretion has remained within the normal range, the endogenous accumulation of benzalkonium chloride , a relatively small amount of exogenous hormones benzalkonium chloride can cause excessive and cause the .

pivaloyl chloride MSDS

1 , pivaloyl chloride
Chinese alias : 2,2 – dimethyl- propionyl chloride ; trimethylammonium chloride ; tert -amyl chloride ; trimethyl acetyl chloride
Name : Pivaloyl chloride
English Name : 2,2-Dimethylpropanoyl chloride; Trimethylacetyl chloride
CAS No. : 3282-30-2
Formula : C5H9ClO
Linear Formula : (CH3) 3CCOCl
Molecular Weight : 120.58
Purity : ≥ 98.0%
No. MDL: MFCD00000709
Beilstein No. : 385668
EC Number: 221-921-6
2 Characters
Colorless oily liquid , soluble in common organic solvents , water and alkali decomposition, flammable
3, the physical parameters
Density : 0.979g/mL (25 ℃)
Boiling point :105-106 ℃
Flash point : 19 ℃
Refractive index (n20 / D): 1.412 (lit.)
4 , hazard statements
Dangerous code : F, T +
Hazard Class :11 -14-22-26-34
Security Level :16-26- 36 / 37/39-45
UN number : UN2438
Domestic hazardous chemicals No. : 81117
5 , the safety data
Hazard Symbols F; T Description
Risk Codes R11; R22; R23; R34 Description
Safety Description S16; S26; S28A; S36/37/39; S38; S45 Description
Transport Information UN 2438
6 Use (Useage)
Pivaloyl chloride is a very important acylating agent , mainly used as pharmaceutical intermediates, as the main raw material for the preparation of amides and many drugs in lipid phenol ; currently used hydroxylamine hydroxylamine benzyl benzyl penicillin and cephalosporins , cefazolin production oxazoline , double pivaloyl adrenaline and other drugs . It is also a lot to do with the production of pesticide intermediates , such Chloropivaloyl chloride.
Chemical synthesis for the protection of the amino group , while increasing the steric effect , the location of a particular product is easily obtained .

Chemical and physical properties of formic acid

Flammable. With water , ethanol , ether and glycerol arbitrary miscible with most polar organic solvents , in hydrocarbons also have some solubility.
Relative density (d204) 1.220. Refractive index
1.3714 . Heat of combustion 254.4 kJ / mol, the critical temperature 306.8 ℃, critical pressure 8.63 MPa. Flash point of 68.9 ℃ ( open cup ) . Density of 1.22 , 1.59 Relative vapor density (air = 1 ) , the saturated vapor pressure (24 ℃) 5.33 kPa.
High concentrations of formic acid in the winter easy to freeze.
Incompatibility: Strong oxidizers , strong alkalis, reactive metal powders.
Hazardous characteristics: its vapor and air can form explosive mixtures case of fire , high- heat combustion caused the explosion. May react with strong oxidizing agents .
Solubility: miscible with water insoluble hydrocarbons , soluble in alcohol.
And the gas in hydrocarbons , the carboxylic acid to form a dimer through hydrogen bonding occurs . In gaseous hydrogen bonds lead to the existence of a large deviation between the acid gas and the ideal gas equation of state . Formic acid by the liquid and solid continuous acid through hydrogen bonding molecules .
Catalytic decomposition of formic acid in concentrated sulfuric acid to CO and H2O:
Due to the special structure of formic acid , one of its hydrogen atoms and carboxyl groups directly connected. Is a hydroxyl group can also be seen as formaldehyde. Therefore, formic acid and formaldehyde , and both properties.
Unlike most other carboxylic acid having the same properties , although not usually an acid chloride or acid anhydride. Acid dehydration decomposition of carbon monoxide and water. Carboxylic acid having reducing aldehydes like . It can play silver mirror reaction, the reduction of silver ions in the ammonia complex silver ions to metallic silver , while he is oxidized into carbon dioxide and water :
Formic acid is the only olefin addition reaction and a carboxylic acid . Carboxylic acid under the action of an acid ( such as sulfuric acid , hydrofluoric acid ) , and the rapid reaction of the olefin ester . However, a side reaction similar to the Koch reaction can also occur , is a more advanced product of a carboxylic acid .
Octanol / water partition coefficient : -0.54 , explosive limit % (V / V): 57.0, lower explosive limit % (V / V): 18.0.
Formic acid is a strong reducing agent , the silver mirror reaction can occur . Saturated fatty acids in the most acidic dissociation constant of 2.1 × 10-4. At room temperature slowly decomposed into carbon monoxide and water. And concentrated sulfuric acid heated to 60 ~ 80 ℃, decompose to release carbon monoxide . Formic acid is heated to above 160 ℃ decomposition that emit carbon dioxide and hydrogen. Alkali metal salts of formic acid was heated to 400 ℃ generated oxalate .
Molecular structure data
1 , the molar refractive index: 8.40
2 , molar volume (m / mol): 39.8
3 , parachor (90.2K): 97.5
4, the surface tension (dyne / cm): 35.8
5 , the polarization ratio (10cm): 3.33

Chlorella Vulgaris Introduction

The Chlorella Vulgaris cells are rich in chlorophyll, are single-celled algae , are eukaryotes.
Photosynthesis is very strong, is several times the other plants. It is rich in protein , vitamins , minerals, dietary fiber , nucleic acids and chlorophyll , is to maintain and promote the health of the essential nutrients , especially glycoproteins contain bioactive substances compelling , polysaccharides and up to 13% nucleic acids and other substances. With enhanced immune to prevent virus proliferation, inhibit cancer cell proliferation , inhibit blood sugar rises , lower serum cholesterol levels, eliminate toxins, rapidly repair damage and other functions of the body. Chlorella Vulgaris is rich in CGF ( Chlorella Vulgaris Growth Factor ) , can quickly restore the damage caused by the body , and as a food flavor improver, widely used in food and fermentation fields. Chlorella Vulgaris is a cell spherical or oval, green , single-celled algae, produced in fresh water or salt water. Freshwater species often grown in more fertile waters , sometimes in the wet soil , rocks, tree trunks can also be found . Under natural conditions, individual water much, but in artificial culture conditions can be a lot of growth and reproduction, high yield, protein content of about 50% of the dry weight , is also rich in other ingredients.
Chlorella Vulgaris algae was first developed protein , in the early 1960s , Japan began to industrial production . Chlorella Vulgaris China Chlorella Vulgaris documented oval , chlorella and pyrenoidosa three kinds , they can be cultured . Similar spirulina , chlorella is not only high in protein , amino acid composition and reasonable , it also contains a lot of rich biological active substances, for many diseases with adjuvant therapy.
Chlorella strong effect on the body several times stronger than spirulina . Chlorella on the heart, liver, kidney lung, stomach , skin, fever and other diseases have a good effect, ate at least a month . Chlorella ability of anti -virus is extremely powerful, but also a strong ability to detoxify drugs .
Chlorella Vulgaris is a world -recognized health food industry, the world’s largest production of microalgae species in Japan, health care products sales in the first ten years in a row , the world’s annual output of 2,000 tons, a major producer of Southeast Asia.