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Benzylamine CAS#100-46-9

CAS Number: 100-46-9
Chemical Formula: C7H9N
Synonyms:

Moringine
moringine[qr]
Sumine 2005

Appearance: Colorless Liquid

MOQ (Minimum Order Quantity): 1 FCL (Full Container Load)

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Product Details

Benzylamine CAS#100-46-9

Colorless to light yellow liquid with a strong odor of ammonia. Floats and mixes with water.

Benzylamine Chemical Properties

Melting point	10 °C (lit.)
Boiling point	184-185 °C (lit.)
density	0.981 g/mL at 25 °C (lit.)
vapor pressure	1.2 hPa (20 °C)
refractive index	n20/D 1.543(lit.)
Fp	140 °F
storage temp.	Store below +30°C.
solubility	alcohol: miscible
form	Liquid
pka	9.33(at 25℃)
color	Clear colorless to slightly yellow
Odor	Strong ammonia.
PH	11.4 (100g/l, H2O, 20℃)
explosive limit	0.7-8.2%(V)
Water Solubility	soluble
Sensitive	Air Sensitive
Merck	14,1125
BRN	741984
Dielectric constant	4.6（Ambient）
Stability:	Combustible. Incompatible with strong oxidizing agents, strong acids.
InChI	1S/C7H9N/c8-6-7-4-2-1-3-5-7/h1-5H,6,8H2
InChIKey	WGQKYBSKWIADBV-UHFFFAOYSA-N
SMILES	NCc1ccccc1
LogP	1 at 25℃
Surface tension	37.1mN/m at 293.15K
CAS DataBase Reference	100-46-9(CAS DataBase Reference)
NIST Chemistry Reference	Benzylamine(100-46-9)
EPA Substance Registry System	Benzylamine (100-46-9)

Safety Information

Hazard Codes	C
Risk Statements	21/22-34
Safety Statements	26-36/37/39-45
RIDADR	UN 2735 8/PG 2
WGK Germany	1
RTECS	DP1488500
F	34
Autoignition Temperature	405 °C
TSCA	TSCA listed
HS Code	2921 49 00
HazardClass	8
PackingGroup	II
Storage Class	8A - Combustible corrosive hazardous materials
Hazard Classifications	Acute Tox. 4 Dermal Acute Tox. 4 Oral Eye Dam. 1 Skin Corr. 1B
Hazardous Substances Data	100-46-9(Hazardous Substances Data)
Toxicity	LD50 orally in Rabbit: 552 mg/kg LD50 dermal Rat 1350 mg/kg

Product Application Of Benzylamine CAS#100-46-9

Benzylamine is a valuable intermediate for various applications and a building block for chemical synthesis used in pharmaceuticals and crop protection agents. It finds application in the coating industry. It is involved as a carrier electrolyte for separation of alkali, alkaline earth and ammonium cations in water samples by capillary electrophoresis with indirect UV detection. It is also used in synthesis of cross-linked porous copolymer supports based on N-(p-vinylbenzoyl)-2-methylalanine, styrene and divinylbenzene. In the textile industry, it is used in colored dyes. It is often used for medicinal purposes in topical creams and antifungal solutions as well as in vitamins.

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