CAS No.144-55-8,Sodium bicarbonate Suppliers,MSDS download

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Basic Information

Molecular Structure:
CAS No.:	144-55-8
Name:	Sodium bicarbonate
Article Data:	524
Cas Database

Formula:	NaHCO₃
Molecular Weight:	84.0069
Synonyms:	Carbonic acid, monosodium salt;Natriumhydrogenkarbonat;Meylon;Carbonic acid disodium salt;SodaSee;Monosodium hydrogen carbonate;Monosodium carbonate;monosodium salt ;; see the subdivided heading;Component of Col-Evac;Soda Mint;Sodium bicarbonate(1:1);Carbonic acid, disodium salt;Natriumbicarbonat, Natriumhydrogencarbonat;Sodium Bicarbonate food grade;
EINECS:	205-633-8
Density:	2.173 g/cm³
Melting Point:	50 °C, 323 K, 122 °F (decomposes)
Boiling Point:	333.6 °C at 760 mmHg
Flash Point:	169.8 °C
Solubility:	in water: 69 g/L (0 °C), 96 g/l (20 °C), 165 g/l (60 °C), 236 g/L (100 °C)
Appearance:	white powder or crystals
Hazard Symbols:	N/A
Risk Codes:	N/A
Safety:	24/25
Transport Information:	N/A
PSA:	60.36000
LogP:	-1.11230

Synthetic route

: 420-04-2
CYANAMID

: 1310-73-2
sodium hydroxide

A: 19981-17-0, 20611-81-8, 123092-13-7, 17292-62-5
sodium cyanamide

B: 144-55-8
sodium hydrogencarbonate

Conditions

Conditions	Yield
In methanol after N. A. Gol'dberg and V. G. Golov, Zh. Prikl. Khim., 35, 2106 (1962);	A 98% B 2%

...Expand

: 124-38-9
carbon dioxide

: 7732-18-5
water

: 7647-14-5
sodium chloride

: 144-55-8
sodium hydrogencarbonate

Conditions

Conditions	Yield
With ammonium chloride In water Gluud-Loepmann process: sepn. of pptd. NaHCO3 and NH4Cl;; very pure product;;	95%
With ammonia In ammonia byproducts: NH4Cl; process includes NH4Cl recovery: treatment with CO2 under pressure;;
With CaHPO4 In water heating CaHPO4 and NaCl in presence of H2O vapor to 700-900°C, treatment of the resulting Na-Ca phosphate in H2O with CO2, formation of NaHCO3 and CaHPO4;;

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: 3-Benzyloxycarbonylamino-1-(2-propyl)-5-(2,2,2-trifluoroethyl)-1,5-benzodiazepine-2-one

A: 3-Amino-1-(2-propyl)-5-(2,2,2-trifluoroethyl)-1,5-benzodiazepine-2-one

B: 144-55-8
sodium hydrogencarbonate

Conditions

Conditions	Yield
In hydrogen bromide; acetic acid	A 88% B n/a

: 108-77-0
1,3,5-trichloro-2,4,6-triazine

: 227626-61-1
(1-carbamoylmethyl-cyclohexylmethyl)-carbamic acid tert-butyl ester

A: 227626-62-2
(1-cyanomethyl-cyclohexylmethyl)-carbamic acid tert-butyl ester

B: 144-55-8
sodium hydrogencarbonate

Conditions

Conditions	Yield
In ice-water; N,N-dimethyl-formamide	A 80% B n/a

...Expand

: 124-38-9
carbon dioxide

A: 141-53-7
sodium formate

B: 144-55-8
sodium hydrogencarbonate

Conditions

Conditions	Yield
With RuCl2((iPr2PCH2CH2)2NH); water; hydrogen; sodium hydroxide at 140℃; under 25858.1 Torr; for 4h; Temperature;	A 71% B 29%
With RuCl2((iPr2PCH2CH2)2NH); water; hydrogen; sodium hydroxide at 130℃; under 25858.1 Torr; for 4h;	A 29.5% B 70.5%

: 177485-96-0
5-[N-tert-butoxycarbonyl-N-[5-(trifluoromethanesulfonamido)pentan-1-yl]aminomethyl]-imidazo[1,2-a]pyridine

: 76-02-8
Trichloroacetyl chloride

A: 177485-97-1
3-trichloroacetyl-5-[N-tert-butoxy-carbonyl-N-[5-(trifluoromethanesulfonamido)pentan-1-yl]aminomethyl]imidazo[1,2-a]pyridine

B: 144-55-8
sodium hydrogencarbonate

Conditions

Conditions	Yield
With dmap In chloroform	A 58.2% B n/a

...Expand

: dinatriumdecacarbonylwolframate

A: 15444-65-2
triphenylphosphine tungsten pentacarbonyl

B: 141-53-7
sodium formate

C: 144-55-8
sodium hydrogencarbonate

D: 497-19-8
sodium carbonate

Conditions

Conditions	Yield
With carbon dioxide; triphenylphosphine In acetonitrile Irradiation (UV/VIS); (Ar or N2); UV irradn. (>420 nm) of soln. of W compd. and PPh3 with stirring at ca. 20°C for ca. 12 h under CO2 pressure, formed ppt. was sepd.; W(CO)5PPh3 was detected IR spect. in filtrate, not isolated; NaHCOO detected 1HNMR spect. in D2O soln. of ppt.; Na2CO3 and NaHCO3 detd. in aq. soln. of ppt. by titrn.;	A 70-90 B 20% C 18% D 39%

...Expand

: Na(1+)*H(1+)*W2(CO)10(2-)=NaHW2(CO)10

A: 15444-65-2
triphenylphosphine tungsten pentacarbonyl

: 16743-03-6, 38800-77-0, 68738-00-1
trans-triphenylphosphane tetracarbonyltungsten

C: 141-53-7
sodium formate

D: 144-55-8
sodium hydrogencarbonate

E: 497-19-8
sodium carbonate

Conditions

Conditions	Yield
With carbon dioxide; triphenylphosphine In acetonitrile Irradiation (UV/VIS); (Ar or N2); UV irradn. (>420 nm) of soln. of W compd. and PPh3 with stirring at ca. 20°C for ca. 12 h under CO2 pressure, formed ppt. was sepd.; W compds. were detected IR spect. in filtrate, not isolated; NaHCOO detected 1HNMR spect. in D2O soln. of ppt.; Na2CO3 and NaHCO3 detd. in aq. soln. of ppt. by titrn.;	A n/a B n/a C 30% D 29% E 27%

...Expand

: 124-38-9
carbon dioxide

: 201230-82-2
carbon monoxide

: 497-19-8
sodium carbonate

A: 141-53-7
sodium formate

B: 62-76-0
sodium oxalate

C: 144-55-8
sodium hydrogencarbonate

Conditions

Conditions	Yield
In neat (no solvent) High Pressure; 2 h at 380°C; cooling, dissolution in water, addn. of HClO4; HPLC;	A 0% B 0% C 0.5%

...Expand

: 179416-72-9
diphenylmethyl α-[4-[4-(4-benzyloxycarbonylamidinophenoxy)butyl]-2,3-dioxopiperazin-1-yl]-α-phenylacetate

A: α-[4-[4-(4-Amidinophenoxy)butyl]-2,3-dioxopiperazin-1yl]-α-phenylacetic acid

B: 144-55-8
sodium hydrogencarbonate

Conditions

Conditions	Yield
With hydrogenchloride; palladium-carbon In N,N-dimethyl-formamide

Raw Materials

4296-19-9

584-08-7

420-04-2

141-53-7

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Specification

Sodium bicarbonate, with the formula NaHCO3, has the IUPAC name of Sodium hydrogen carbonate. It is a white solid that is crystalline but often appears as a fine powder. It will melt at 50 °C which is soluble in water. It is stable at normal pressure and temperature. The substance should be stored at cool, dry, well-ventilated place. In addition, it should be protected from strong oxides and acids. Sodium bicarbonate is amphoteric which can react with acids and bases. With the CAS register number of 144-55-8, the substance also has the EINECS registry number 205-633-8. Sodium bicarbonate is a component of the mineral natron and is found dissolved in many mineral springs. The substance is an amphoteric compound. Aqueous solutions are mildly alkaline due to the formation of carbonic acid and hydroxide ion. Sodium bicarbonate reacts with bases such as sodium hydroxide to form carbonates. Sodium bicarbonate and an acid can react to give a salt and carbonic acid which readily decomposes to give carbon dioxide and water. Sodium bicarbonate will gradually decompose into sodium carbonate and carbon dioxide above 70 °C. The conversion is more fast at 200 °C.When you are using this chemical, please be cautious about it as the following: please avoid contact with skin and eyes.

Physical properties about Sodium bicarbonate are:
(1)ACD/LogP: -0.809; (2)ACD/LogD (pH 5.5): -1.98; (3)ACD/LogD (pH 7.4): -3.77; (4)ACD/BCF (pH 5.5): 1.00; (5)ACD/BCF (pH 7.4): 1.00; (6)ACD/KOC (pH 5.5): 1.00; (7)ACD/KOC (pH 7.4): 1.00; (8)#H bond acceptors: 3 ; (9)#H bond donors: 2 ; (10)Polar Surface Area: 46.53 ?2 ; (11)Polarizability: 10-24cm³; (12)Flash Point: 169.8 °C; (13)Enthalpy of Vaporization: 63.37 kJ/mol; (14)Boiling Point: 333.6 °C at 760 mmHg; (15)Vapour Pressure: 2.58E-05 mmHg at 25°C

Preparation of Sodium bicarbonate:
Sodium bicarbonate is mainly prepared by the Solvay process, which is the reaction of calcium carbonate, sodium chloride, ammonia, and carbon dioxide in water. It may be obtained by the reaction of carbon dioxide with an aqueous solution of sodium hydroxide. The initial reaction produces sodium carbonate. Further addition of carbon dioxide produces sodium bicarbonate.
CO₂ + 2 NaOH → Na₂CO₃ + H₂O
Na₂CO₃ + CO₂ + H₂O → 2 NaHCO₃

Uses of Sodium bicarbonate:
The Sodium bicarbonate was used as a cleansing agent like soap. Sodium bicarbonate was sometimes used in cooking vegetables, to make them softer. As a leavening agent, Sodium bicarbonate is primarily used in cooking. Sodium bicarbonate can be used as a wash to remove any acidic impurities from a "crude" liquid, producing a purer sample. Sodium bicarbonate can be added as a simple solution for raising the pH balance of water. Sodium bicarbonate is used in an aqueous solution as an antacid. Sodium bicarbonate is sold as a cattle feed supplement, in particular as a buffering agent for the rumen. It may also be used in an oral form to treat chronic forms of metabolic acidosis such as chronic renal failure and renal tubular acidosis. Sodium bicarbonate may also be used in urinary alkalinization for the treatment of aspirin overdose and uric acid renal stones. It is used as the medicinal ingredient in gripe water for infants. It is used as well for treatment of hyperkalemia. Sodium bicarbonate can be used as an exfoliant. Small amounts of Sodium bicarbonate have been shown to be useful as a supplement for endurance athletes. Sodium bicarbonate can be used to extinguish small grease or electrical fires by being thrown over the fire. However, as it may cause the grease to splatter, it should not be applied to fires in deep fryers.

You can still convert the following datas into molecular structure:
(1)Canonical SMILES: C(=O)(O)[O-].[Na+]
(2)InChI: InChI=1S/CH2O3.Na/c2-1(3)4;/h(H2,2,3,4);/q;+1/p-1
(3)InChIKey: UIIMBOGNXHQVGW-UHFFFAOYSA-M

The toxicity data of Sodium bicarbonate is as follows:

Organism	Test Type	Route	Reported Dose (Normalized Dose)	Effect	Source
infant	TDLo	oral	1260mg/kg (1260mg/kg)	LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES KIDNEY, URETER, AND BLADDER: URINE VOLUME INCREASED	American Journal of Diseases of Children. Vol. 135, Pg. 965, 1981.
man	TDLo	oral	20mg/kg/5D-I (20mg/kg)	GASTROINTESTINAL: NAUSEA OR VOMITING	American Journal of Emergency Medicine. Vol. 12, Pg. 57, 1994.
mouse	LD50	oral	3360mg/kg (3360mg/kg)		Gigiena Truda i Professional'nye Zabolevaniya. Labor Hygiene and Occupational Diseases. Vol. 33(5), Pg. 30, 1989.
rat	LC	inhalation	> 900mg/m³ (900mg/m³)		Gigiena Truda i Professional'nye Zabolevaniya. Labor Hygiene and Occupational Diseases. Vol. 33(5), Pg. 30, 1989.
rat	LD50	oral	4220mg/kg (4220mg/kg)		Toxicology and Applied Pharmacology. Vol. 6, Pg. 726, 1964.

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