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A4303712

Formate , StandardforGC,>99% , 64-18-6

Synonym(s):
Formic acid;Methanoic acid solution, Formylic acid solution;Methanoic acid, Formylic acid;Methanoic Acid,Aminic Acid;Methanoic Acid,Aminic Acid, Aminic Acid

CAS NO.:64-18-6

Empirical Formula: CH2O2

Molecular Weight: 46.03

MDL number: MFCD00003274

EINECS: 200-579-1

Update time: 2022-07-08

PRODUCT Properties

Melting point: 8.2-8.4 °C (lit.)
Boiling point: 100-101 °C (lit.)
Density  1.22 g/mL at 25 °C (lit.)
vapor density  1.03 (vs air)
vapor pressure  52 mm Hg ( 37 °C)
refractive index  n20/D 1.377
FEMA  2487 | FORMIC ACID
Flash point: 133 °F
storage temp.  2-8°C
solubility  H2O: soluble1g/10 mL, clear, colorless
pka 3.75(at 20℃)
form  Liquid
Specific Gravity 1.216 (20℃/20℃)
color  APHA: ≤15
PH 3.47(1 mM solution);2.91(10 mM solution);2.38(100 mM solution);
Odor at 0.10 % in water. pungent vinegar formyl
Odor Type acetic
explosive limit 12-38%(V)
Water Solubility  MISCIBLE
Sensitive  Hygroscopic
λmax λ: 260 nm Amax: 0.03
λ: 280 nm Amax: 0.01
Merck  14,4241
JECFA Number 79
BRN  1209246
Henry's Law Constant At 25 °C: 95.2, 75.1, 39.3, 10.7, and 3.17 at pH values of 1.35, 3.09, 4.05, 4.99, and 6.21, respectively (Hakuta et al., 1977)
Dielectric constant 58.0(16℃)
Exposure limits TLV-TWA 5 ppm (~9 mg/m3) (ACGIH, MSHA, OSHA, and NIOSH); IDLH 100 ppm (180 mg/m3) (NIOSH).
Stability: Stable. Substances to be avoided include strong bases, strong oxidizing agents and powdered metals, furfuryl alcohol. Combustible. Hygroscopic. Pressure may build up in tightly closed bottles, so bottles should be opened carefully and vented periodically.
InChIKey BDAGIHXWWSANSR-UHFFFAOYSA-N
LogP -0.540
CAS DataBase Reference 64-18-6(CAS DataBase Reference)
NIST Chemistry Reference Formic acid(64-18-6)
EPA Substance Registry System Formic acid (64-18-6)

Description and Uses

Formic acid is a clear, colorless liquid with a pungent odor. Formic acid was first isolated from certain ants and was named after the Latin formica, meaning ant. It is made by the action of sulfuric acid on sodium formate, which is produced from carbon monoxide and sodium hydroxide. It is also produced as a by-product in the manufacture of other chemicals such as acetic acid.
It can be anticipated that use of formic acid will continuously increase as it replaces inorganic acids and has a potential role in new energy technology. Formic acid toxicity is of a special interest as the acid is the toxic metabolite of methanol.

Formic acid has a number of commercial uses. It is used in the leather industry to degreaseand remove hair from hides and as an ingredient in tanning formulations. It is used as alatex coagulant in natural rubber production. Formic acid and its formulations are used aspreservatives of silage. It is especially valued in Europe where laws require the use of naturalantibacterial agents rather than synthetic antibiotics. Silage is fermented grass and crops thatare stored in silos and used for winter feed. Silage is produced during anaerobic fermentationwhen bacteria produce acids that lower the pH, preventing further bacterial action. Acetic acidand lactic acid are the desired acids during silage fermentation. Formic acid is used in silageprocessing to reduce undesirable bacteria and mold growth. Formic acid reduces Clostridiabacteria that would produce butyric acid causing spoilage. In addition to preventing silagespoilage, formic acid helps preserve protein content, improves compaction, and preservessugar content. Formic acid is used as a miticide by beekeepers.

Safety

Symbol(GHS) 
GHS05,GHS06
Signal word  Danger
Hazard statements  H302-H314-H331
Precautionary statements  P261-P280-P301+P312-P303+P361+P353-P304+P340+P310-P305+P351+P338
Hazard Codes  T,C,Xi
Risk Statements  23/24/25-34-40-43-35-36/38-10
Safety Statements  36/37-45-26-23-36/37/39
RIDADR  UN 1198 3/PG 3
OEB B
OEL TWA: 5 ppm (9 mg/m3)
WGK Germany  2
RTECS  LP8925000
10
Autoignition Temperature 1004 °F
TSCA  Yes
HazardClass  8
PackingGroup  II
HS Code  29151100
Hazardous Substances Data 64-18-6(Hazardous Substances Data)
Toxicity LD50 in mice (mg/kg): 1100 orally; 145 i.v. (Malorny)
IDLA 30 ppm

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