CAS No.75-12-7,Formamide Suppliers,MSDS download

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Basic Information

Molecular Structure:
CAS No.:	75-12-7
Name:	Formamide
Article Data:	2

Formula:	CH₃NO
Molecular Weight:	45.0409
Synonyms:	Carbamaldehyde;Formimidic acid;Methanamide;NSC 748;
EINECS:	200-842-0
Density:	0.978 g/cm³
Melting Point:	2-3 °C
Boiling Point:	210.5 °C at 760 mmHg
Flash Point:	81.1 °C
Solubility:	miscible with water
Appearance:	colorless liquid
Hazard Symbols:	T
Risk Codes:	61-41-37/38
Safety:	53-45-36/37/39-26-23
PSA:	43.09000
LogP:	0.43770

Raw Materials

77287-34-4

Total:204 Page 1 of 6 1 2 3 4 5 6 Next>>

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Consensus Reports

Reported in EPA TSCA Inventory. EPA Genetic Toxicology Program.

Standards and Recommendations

OSHA PEL: TWA 20 ppm; STEL 30 ppm
ACGIH TLV: TWA 10 ppm (skin)

Specification

The IUPAC name of this chemical is Formamide. With the CAS registry number 75-12-7, it is also named as Amid kyseliny mravenci. The product's categories are FM - FZAnalytical Standards; Alphabetical Listings; E-FAlphabetic; NMR Reference Standards; NMR Stable Isotopes; Spectroscopy; Stable Isotopes. It is colorless liquid with a faint odor of ammonia, which is miscible with water, alcohol, ethylene glycol, acetone, acetic acid, glycerin and phenol, and almost insoluble in aliphatic hydrocarbons, aromatic hydrocarbons, ethers, chlorinated hydrocarbons, chlorobenzene, nitrobenzene, etc. Formamide will begin to partially decompose into carbon monoxide and ammonia at 180°C. When heated strongly, formamide decomposes to hydrogen cyanide (HCN) and water vapor. Reacts with water very slowly at room temperature, but rate is accelerated by acids and bases at elevated temperatures. Additionally, this chemical should be sealed in the container and stored in the cool and dry place.

Physical properties about Formamide are: (1)ACD/LogP: -1.51; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): -1.51; (4)ACD/LogD (pH 7.4): -1.51; (5)ACD/BCF (pH 5.5): 1; (6)ACD/BCF (pH 7.4): 1; (7)ACD/KOC (pH 5.5): 3.59; (8)ACD/KOC (pH 7.4): 3.59; (9)#H bond acceptors: 2; (10)#H bond donors: 2; (11)#Freely Rotating Bonds: 0; (12)Index of Refraction: 1.369; (13)Molar Refractivity: 10.4 cm³; (14)Molar Volume: 46 cm³; (15)Polarizability: 4.12×10^-24 cm³; (16)Surface Tension: 32.4 dyne/cm; (17)Enthalpy of Vaporization: 44.68 kJ/mol; (18)Vapour Pressure: 0.192 mmHg at 25°C; (19)Tautomer Count: 2; (20)Exact Mass: 45.021464; (21)MonoIsotopic Mass: 45.021464; (22)Topological Polar Surface Area: 43.1; (23)Heavy Atom Count: 3; (24)Complexity: 12.3.

Preparation of Formamide: It can be obtained by the aminolysis of methyl formate.
HCOOCH₃ + NH₃ → HCONH₂ + CH₃OH
In the past, formic acid was reacted with ammonia to produce ammonium formate, which was turned into formamide by heating.

Uses of Formamide: It is used primarily for manufacturing sulfa drugs and synthesizing vitamins and as a softener for paper and fiber. It is also a constituent of cryoprotectant vitrification mixtures used for cryopreservation of tissues and organs. In addition, its pure form can used as a solvent. And it is also used as an RNA stabiliser in gel electrophoresis by deionizing RNA. Besides, Formamide can react with piperidine to get 1-formyl-piperidine. The yield is 87%.

When you are using this chemical, please be cautious about it as the following:
It is irritating to respiratory system and skin. It also can cause serious damage to the eyes and may cause harm to the unborn child. So people should not breathe vapour. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. If you want to contact this product, you must wear suitable protective clothing, gloves and eye/face protection. In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)

People can use the following data to convert to the molecule structure.
1. SMILES:O=CN
2. InChI:InChI=1/CH3NO/c2-1-3/h1H,(H2,2,3)
3. InChIKey:ZHNUHDYFZUAESO-UHFFFAOYAQ

The following are the toxicity data which has been tested.

Organism	Test Type	Route	Reported Dose (Normalized Dose)	Effect	Source
dog	LDLo	intravenous	1500mg/kg (1500mg/kg)		"Abdernalden's Handbuch der Biologischen Arbeitsmethoden." Vol. 4, Pg. 1289, 1935.
frog	LDLo	subcutaneous	30mg/kg (30mg/kg)		"Abdernalden's Handbuch der Biologischen Arbeitsmethoden." Vol. 4, Pg. 1289, 1935.
guinea pig	LD50	intraperitoneal	1250mg/kg (1250mg/kg)	BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) AUTONOMIC NERVOUS SYSTEM: OTHER (DIRECT) PARASYMPATHOMIMETIC	Toksikologiya Novykh Promyshlennykh Khimicheskikh Veshchestv. Toxicology of New Industrial Chemical Substances. For English translation, see TNICS*. Vol. 9, Pg. 163, 1967.
mammal (species unspecified)	LD50	oral	3150mg/kg (3150mg/kg)		Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 39(4), Pg. 86, 1974.
mouse	LD50	intraperitoneal	2450mg/kg (2450mg/kg)		Naunyn-Schmiedeberg's Archiv fuer Experimentelle Pathologie und Pharmakologie. Vol. 230, Pg. 559, 1957.
mouse	LD50	oral	3150mg/kg (3150mg/kg)		Toksikologiya Novykh Promyshlennykh Khimicheskikh Veshchestv. Toxicology of New Industrial Chemical Substances. For English translation, see TNICS*. Vol. 11, Pg. 86, 1969.
rabbit	LD50	skin	17gm/kg (17000mg/kg)		National Technical Information Service. Vol. OTS0528421,
rat	LC50	inhalation	> 3900ppm/6H (3900ppm)		National Technical Information Service. Vol. OTS0528421,
rat	LD	skin	> 13500mg/kg (13500mg/kg)		Polish Journal of Pharmacology and Pharmacy. Vol. 32, Pg. 223, 1980.
rat	LD50	intraperitoneal	5700mg/kg (5700mg/kg)		Toxicology and Applied Pharmacology. Vol. 26, Pg. 596, 1973.
rat	LD50	oral	5577mg/kg (5577mg/kg)	KIDNEY, URETER, AND BLADDER: INCONTINENCE BEHAVIORAL: ATAXIA AUTONOMIC NERVOUS SYSTEM: OTHER (DIRECT) PARASYMPATHOMIMETIC	Toksikologiya Novykh Promyshlennykh Khimicheskikh Veshchestv. Toxicology of New Industrial Chemical Substances. For English translation, see TNICS*. Vol. 9, Pg. 163, 1967.
rat	LD50	subcutaneous	> 4gm/kg (4000mg/kg)		Naunyn-Schmiedebergs Archiv fuer Pharmakologie und Experimentelle Pathologie. Vol. 257, Pg. 296, 1967.
rat	LD50	unreported	3gm/kg (3000mg/kg)		Experientia. Vol. 29, Pg. 225, 1973.