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25895-60-7

Sodium cyanoborohydride

CAS: 25895-60-7

Molecular Formula: CH3BNNa

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25895-60-7 - Names and Identifiers

Name Sodium cyanoborohydride
Synonyms Sodium cyanoborohydride
SodiuM cyanohydridoborate
Sodium cyanotrihydroborate
Sodium cyanotrihydridoborate
SodiuM (T-4)-(Cyano-C)trihydroborate(1-)
(cyano-C)trihydro-,sodium,(T-4)-Borate(1-)
sodium (cyano-kappaC)(trihydrido)borate(1-)
sodium,(beta-4)-borate(1-(cyano-c)trihydro-
Sodium cyanoborohydride,Sodium cyanotrihydridoborate
CAS 25895-60-7
EINECS 247-317-2
InChI InChI=1/CH3BN.Na/c2-1-3;/h2H3;/q-1;+1

25895-60-7 - Physico-chemical Properties

Molecular FormulaCH3BNNa
Molar Mass62.84
Density1.083g/mLat 25°C
Melting Point>242 °C (dec.) (lit.)
Boling Point307°C
Flash Point−1°F
Water Solubility2120 g/L at 29 ºC (dec.)
Solubility Soluble in water (100 mg/ml, with heating), methanol, ethanol, and THF. It is insoluble in nonpolar solvents such as benzene or hexane
AppearancePowder
Specific Gravity1.2
ColorWhite
Merck14,8606
BRN4152656
Storage ConditionStore below +30°C.
StabilityStable. Hygroscopic. Reacts violently with water, giving off and igniting hydrogen. Do not use water on fires involving this chemical - instead use dry soda ash. Incompatible with strong acids, water
SensitiveMoisture Sensitive
Physical and Chemical PropertiesWhite or yellowish solid powder is a mild reducing agent, which is widely used in the reduction of aldehydes and ketones, especially the reductive amination of ketones.

25895-60-7 - Risk and Safety

Risk CodesR26/27/28 - Very toxic by inhalation, in contact with skin and if swallowed.
R32 - Contact with acids liberates very toxic gas
R34 - Causes burns
R50/53 - Very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment. 
R16 - Explosive when mixed with oxidizing substances
R15 - Contact with water liberates extremely flammable gases
R11 - Highly Flammable
R51/53 - Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment. 
R36 - Irritating to the eyes
R23/24/25 - Toxic by inhalation, in contact with skin and if swallowed.
R19 - May form explosive peroxides
R14 - Reacts violently with water
R40 - Limited evidence of a carcinogenic effect
R36/37/38 - Irritating to eyes, respiratory system and skin.
Safety DescriptionS26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S28 - After contact with skin, wash immediately with plenty of soap-suds.
S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.
S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
S60 - This material and its container must be disposed of as hazardous waste.
S61 - Avoid release to the environment. Refer to special instructions / safety data sheets. 
S8 - Keep container dry.
S50A -
S43 - In case of fire use ... (there follows the type of fire-fighting equipment to be used.)
S28A -
S1 - Keep locked up.
S16 - Keep away from sources of ignition.
S36/37 - Wear suitable protective clothing and gloves.
UN IDsUN 3179 4.1/PG 2
WGK Germany1
FLUKA BRAND F CODES10-21
TSCAYes
HS Code28500020
Hazard NoteToxic/Highly Flammable
Hazard Class6.1
Packing GroupI

25895-60-7 - Reference Information

EPA chemical information Information provided by: ofmpub.epa.gov (external link)
introduction sodium cyanoborohydride is a chemical substance, white or yellowish solid powder, and a mild reducing agent.
Application Sodium cyanoborohydride is widely used in the reduction of aldehydes and ketones, especially the reductive amination of ketones. It is a reducing agent for organic synthesis, aldehydes, ketones, oximes, enamines are reduced, β-lactam is reduced to β-amino acids, and ammonia is methylated.
reducibility although sodium cyanoborohydride (NaBH3CN) is weaker than sodium borohydride, it can remain stable in an acidic environment with pH 3. Therefore, it is often used to reduce imine cations in acidic environments. (Borch reductive amination)
Use is a mild reducing agent, which is widely used for the reduction of aldehydes and ketones, especially the reductive amination of ketones.
Reducing agents for organic synthesis, aldehydes, ketones, oximes, enamines are reduced, and β-lactam is reduced to β-amino acids. Methylation of ammonia.
Last Update:2024-04-09 20:52:54
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