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ChemicalBook >> CAS DataBase List >>3-Aminobenzylamine

3-Aminobenzylamine

CAS No.
4403-70-7
Chemical Name:
3-Aminobenzylamine
Synonyms
3-(AMINOMETHYL)ANILINE;3-AminobenzyL;m-Aminobenzylamine;3-AMINOBENZYLAMINE;RARECHEM AL BW 0272;m-Aminomethylaniline;Meta aminobenzylamine;3-Aminobenzylamine,97%;3-Aminobenzylamine 99%;3-Aminobenzylamine >
CBNumber:
CB8263063
Molecular Formula:
C7H10N2
Molecular Weight:
122.17
MDL Number:
MFCD00078355
MOL File:
4403-70-7.mol
MSDS File:
SDS
Last updated:2026-05-28 05:38:49
Product description Number Pack Size Price
3-Aminobenzylamine 99% 721492 5g $98.8
3-Aminobenzylamine 99% 721492 25g $126
3-Aminobenzylamine >98.0%(GC)(T) A1431 5g $44
3-Aminobenzylamine >98.0%(GC)(T) A1431 25g $121
3-(Aminomethyl)aniline 98% OR16072 25g $22
More product size

3-Aminobenzylamine Properties

Melting point 41-45 °C
Boiling point 134°C/4mmHg(lit.)
Density 1.093±0.06 g/cm3(Predicted)
Flash point >110℃
storage temp. 2-8°C, protect from light
solubility soluble in Methanol
pka 9.22±0.10(Predicted)
form Low Melting Solid
color Pale brown
InChI 1S/C7H10N2/c8-5-6-2-1-3-7(9)4-6/h1-4H,5,8-9H2
InChIKey ZDBWYUOUYNQZBM-UHFFFAOYSA-N
SMILES NCc1cccc(N)c1
CAS DataBase Reference 4403-70-7(CAS DataBase Reference)
EWG's Food Scores 1
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Corrosion (GHS05)Exclamation Mark (GHS07)Environment (GHS09)
GHS05,GHS07,GHS09
Signal word  Danger
Hazard statements  H302-H314-H410
Precautionary statements  P260-P273-P280-P301+P330+P331-P303+P361+P353-P305+P351+P338
Hazard Codes  N,C
Risk Statements  34-51/53-22
Safety Statements  26-36/37/39-61-45-22
RIDADR  3259
WGK Germany  3
TSCA  TSCA listed
HazardClass  8
PackingGroup  III
HS Code  29215900
Storage Class 8B - Non-combustible corrosive hazardous materials
Hazard Classifications Acute Tox. 4 Oral
Aquatic Acute 1
Aquatic Chronic 1
Eye Dam. 1
Skin Corr. 1B
REACH Registrations Inactive
NFPA 704
1
3 0

3-Aminobenzylamine price More Price(38)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 721492 3-Aminobenzylamine 99% 4403-70-7 5g $98.8 2023-06-20 Buy
Sigma-Aldrich 721492 3-Aminobenzylamine 99% 4403-70-7 25g $126 2022-05-15 Buy
TCI Chemical A1431 3-Aminobenzylamine >98.0%(GC)(T) 4403-70-7 5g $44 2026-04-30 Buy
TCI Chemical A1431 3-Aminobenzylamine >98.0%(GC)(T) 4403-70-7 25g $121 2026-04-30 Buy
Apolloscientific OR16072 3-(Aminomethyl)aniline 98% 4403-70-7 25g $22 2026-06-04 Buy
Product number Packaging Price Buy
721492 5g $98.8 Buy
721492 25g $126 Buy
A1431 5g $44 Buy
A1431 25g $121 Buy
OR16072 25g $22 Buy

3-Aminobenzylamine Chemical Properties,Uses,Production

Application

m-Aminobenzylamine is an important organic dye and pharmaceutical intermediate. It can also be used as a curing agent for epoxy resins and in the polymerization of olefin compounds to prepare insulated cables. Synthetic methods for benzylamine compounds include the reaction of benzaldehyde with hydroxylamine hydrochloride, direct amination of halobenzyl with aminoamine, amination with hexamethylenetetramine, and amination with phthalimide. Alfred prepared m-aminobenzylamine using m-nitrobenzoic acid as a raw material; other methods involve introducing a CN group onto the benzene ring followed by catalytic hydrogenation.

Chemical Properties

Pale brown low melting solid

Synthesis Reference(s)

Synthetic Communications, 25, p. 863, 1995 DOI: 10.1080/00397919508013422

Synthesis

(Z)-3-Nitrobenzaldehyde oxime

3717-30-4

3-Aminobenzylamine

4403-70-7

The general procedure for the synthesis of 3-aminobenzylamine from the compound (CAS:3717-30-4) is as follows: Example 18: 16.6 g (0.1 mol) of m-nitrobenzaldehyde oxime made in Example 15, 9.5 g (0.05 mol) of p-toluenesulfonic acid, 0.5 g of 5% Pt-C catalyst and 75 mL of dioxane were added to a sealed glass vessel. Vigorous stirring was carried out under hydrogen-filled conditions. The reaction was continued at 30°C to 40°C for 8 hours. Upon completion of the reaction, the mixture was filtered to remove the catalyst, followed by the addition of 35 g (0.3 mol) of 35% aqueous sodium hydroxide. After stirring, the mixture was allowed to stand until layered. The lower layer was separated and discarded and the upper layer was distilled. Finally 8.9 g of m-aminobenzylamine was obtained in 72.9% yield and 99.3% purity by gas chromatography.

References

[1] Patent: US4751328, 1988, A

Global( 246)Suppliers
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View Lastest Price from 3-Aminobenzylamine manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
3-Aminobenzylamine  pictures 2025-11-18 3-Aminobenzylamine
4403-70-7
$1.10 1g 99.0% Min 100 Tons Dideu Industries Group Limited
3-Aminobenzylamine pictures 2025-06-27 3-Aminobenzylamine
4403-70-7
1KG 99% 500000kg Hebei Chuanghai Biotechnology Co., Ltd
3-Aminobenzylamine pictures 2025-04-04 3-Aminobenzylamine
4403-70-7
1kg 98% 1Ton Henan Aochuang Chemical Co.,Ltd.
RARECHEM AL BW 0272 3-AMINOBENZYLAMINE 3-(Aminomethyl)benzenamine 3-Aminobenzenemethanamine m-Aminomethylaniline 3-Aminobenzylamine,97% 3-Aminobenzylamine, (3-Aminophenyl)methylamine ALPHA-AMINO-M-TOLUIDINE m-Aminobenzylamine 3-AMinobenzylaMine, 97% 5GR 3-(Aminomethyl)aniline alpha-Amino-m-toluidine 3-AMinobenzylaMine 2HCl 3-Aminobenzylamine 99% 3-Aminobenzene methylamine 3-Aminobenzylamine, 98%, reagent grade 3-Aminobenzylamine > 3-AminobenzyL Benzenemethanamine, 3-amino- 3-Aminobenzylamine ISO 9001:2015 REACH 3-(AMINOMETHYL)ANILINE 3-Aminobenzylamine,reagentgrade Meta aminobenzylamine 3-AminobenzeneChemicalbookmethanamine 4403-70-7 4403-79-7 NH2C6H4CH2NH2 Anilines, Aromatic Amines and Nitro Compounds Amine Amines amine series
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