3-Iodobenzylamine hydrochloride

Product Name: 3-Iodobenzylamine hydrochloride
CAS No.: 3718-88-5
Chemical Name: 3-Iodobenzylamine hydrochloride
Synonyms: 3-IODOBENZYLAMINE HCL;(3-iodophenyl)MethanaMine hydrochloride;Trimethoprim Impurity 29;3-Iodo-benzenemethanamine HCl;3-IODOBENZYLAMINE HYDROCHLORIDE;3-lodobenzylamine hydrochloride;M-IODOBENZYLAMINE HYDROCHLORIDE;3-IodobenzylamineHydrochloride>3-Iodobenzylamine hydrochloride 97%;3-Iodobenzylamine hydrochloride,97%
CBNumber: CB3324936
Molecular Formula: C7H9ClIN
Formula Weight: 269.51
MOL File: 3718-88-5.mol

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3-Iodobenzylamine hydrochloride Property

Melting point:: 188-190 °C(lit.)
storage temp.: Keep in dark place,Inert atmosphere,Room temperature
Water Solubility: Soluble in water
form: powder to crystal
color: White to Light yellow
Sensitive: Light Sensitive
BRN: 5352277
InChI: InChI=1S/C7H8IN.ClH/c8-7-3-1-2-6(4-7)5-9;/h1-4H,5,9H2;1H
InChIKey: PYFDZOCGFHIRST-UHFFFAOYSA-N
SMILES: C(C1C=CC=C(I)C=1)N.Cl
CAS DataBase Reference: 3718-88-5(CAS DataBase Reference)

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Safety

Hazard Codes: Xi,T,Xn
Risk Statements: 36/37/38-63-42/43
Safety Statements: 24/25-36/37/39-26-23-22
WGK Germany: 3
Hazard Note: Irritant/Light Sensitive
HS Code: 29214990

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Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Danger

Hazard statements

H315Causes skin irritation

H317May cause an allergic skin reaction

H319Causes serious eye irritation

H334May cause allergy or asthma symptoms or breathing difficulties if inhaled

H335May cause respiratory irritation

H361Suspected of damaging fertility or the unborn child

Precautionary statements

P201Obtain special instructions before use.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P308+P313IF exposed or concerned: Get medical advice/attention.

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N-Bromosuccinimide Price

Sigma-Aldrich

Product number: 134996
Product name: 3-Iodobenzylamine hydrochloride
Purity: 97%
Packaging: 5g
Price: $341
Updated: 2025/07/31

TCI Chemical

Product number: I0710
Product name: 3-Iodobenzylamine Hydrochloride
Purity: >98.0%(HPLC)
Packaging: 1g
Price: $28
Updated: 2025/07/31

TCI Chemical

Product number: I0710
Product name: 3-Iodobenzylamine Hydrochloride
Purity: >98.0%(HPLC)
Packaging: 5g
Price: $85
Updated: 2025/07/31

TRC

Product number: I689530
Product name: 3-Iodobenzylamine hydrochloride
Packaging: 25g
Price: $415
Updated: 2021/12/16

American Custom Chemicals Corporation

Product number: HCH0021988
Product name: 3-IODOBENZYLAMINE HYDROCHLORIDE
Purity: 95.00%
Packaging: 1G
Price: $613.88
Updated: 2021/12/16

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3-Iodobenzylamine hydrochloride Chemical Properties,Usage,Production

Chemical Properties

white to light yellow crystal powde

Uses

3-Iodobenzylamine hydrochloride was used as the starting reagent in the synthesis of N⁶-(3-iodobenzyl)-2-substituted-adenosine derivatives. It was used in the synthesis of 3′-C-methyl adenosine N⁶-substituted and N⁶/C-2 disubstituted derivatives and novel 2′-C-methyl analogues.

Synthesis

200706-60-1

3718-88-5

The general procedure for the synthesis of 3-iodobenzylamine hydrochloride from the compound (CAS: 200706-60-1) was as follows: 2.0 g (5.6 mmol) of compound (A) and 20 mL of anhydrous ethanol were added to the reaction flask. After heating the mixture to 60°C, an ethanolic solution of hydrazine hydrate (prepared by dissolving 0.42 g, 8.4 mmol of hydrazine hydrate in 3 mL of anhydrous ethanol) was added dropwise under continuous stirring. The reaction was kept heated and stirred for 20 min and a yellow precipitate was observed to be formed. Stirring was stopped and the reaction mixture was kept in a 70°C water bath for 2.5 hours. It was then cooled to room temperature, at which time a large amount of yellow precipitate precipitated. 4 mL of 1 mol/L hydrochloric acid solution was added to the reaction flask to acidify the reaction mixture and stirring was continued for 30 minutes. After completion of the reaction, a filtration operation was carried out, the filtrate was washed with a small amount of water and the filtrates were combined. The combined filtrates were evaporated to dryness under reduced pressure and finally dried under vacuum to give 0.539 g of yellow solid (B) in 35.9% yield.

References

[1] Patent: CN106187823, 2016, A. Location in patent: Paragraph 0028; 0029

3-Iodobenzylamine hydrochloride Preparation Products And Raw materials

Raw materials

Preparation Products

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3-Iodobenzylamine hydrochloride Suppliers

Americas 1 Belgium 1 China 136 Europe 3 Germany 3 India 20 Japan 3 Slovakia 1 Switzerland 2 Ukraine 2 United Kingdom 14 United States 32 Global 218

Shanghai Jiyu Medical Technology Co., Ltd

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View Lastest Price from 3-Iodobenzylamine hydrochloride manufacturers

Hebei Chuanghai Biotechnology Co., Ltd

Product: 3-Iodobenzylamine hydrochloride 3718-88-5
Price: US $0.00-0.00/KG
Min. Order: 1KG
Purity: 99%
Supply Ability: 20 mt
Release date: 2024-11-15

Hebei Chuanghai Biotechnology Co,.LTD

Product: 3-Iodobenzylamine hcl 3718-88-5
Price: US $9.00/KG
Min. Order: 1KG
Purity: 99.8%
Supply Ability: 100tons
Release date: 2024-08-16

Zhuozhou Wenxi import and Export Co., Ltd

Product: 3-Iodobenzylamine hydrochloride 3718-88-5
Price: US $15.00-10.00/KG
Min. Order: 1KG
Purity: 99%+ HPLC
Supply Ability: Monthly supply of 1 ton
Release date: 2021-07-10

3718-88-5, 3-Iodobenzylamine hydrochlorideRelated Search:

3-Iodobenzylamine Methoxyammonium chloride Benzylamine hydrochloride Dibenzylamine 4-Hydroxybenzylamine Triethylamine hydrochloride Phenoxybenzamine hydrochloride Topotecan hydrochloride 2,3,4-TRIMETHOXYPHENYLACETIC ACID TriMethopriM IMpurity C 3-Iodobenzyl bromide 2,3,4-Trihydroxybenzaldehyde 3-Anilino-2-(3,4,5-triMethoxybenzyl)acrylonitrile, (Mixture of cis/trans isoMers) Trimethoprim Related Compound B (25 mg) (2,4-diaminopyrimidin-5-yl)(3,4,5-trimethoxyphenyl)methanone) (AS) 1,4-Bis(2,3,4-triMethoxybenzyl)piperazine 4-[(2,3,4-TriMethoxyphenyl)Methyl]-1-piperazinecarboxylic Acid Ethyl Ester 1-Dimethylamino-2-phenylbutan-2-yl 3,4,5-trimethoxybenzoate 1-(3,4,5-TRIMETHOXY-BENZYL)-PIPERAZINE

3-IODOBENZYLAMINE HCL

3-IODOBENZYLAMINE HYDROCHLORIDE

3-iodo-benzenemethanaminhydrochloride

M-IODOBENZYLAMINE HYDROCHLORIDE

3-lodobenzylamine hydrochloride

3-IODOBENZYLAMINE HYDROCHLORIDE, 98+%

3-Iodobenzylamine hydrochloride,97%

3-IodobenzylaMine hydrochloride, 97% 1GR

(3-iodophenyl)MethanaMine hydrochloride

3-Iodobenzylamine hydrochloride 97%

3-IodobenzylamineHydrochloride&gt

Benzenemethanamine, 3-iodo-, hydrochloride

3-Iodobenzylamine hydrochloride ISO 9001：2015 REACH

Benzylamine, m-iodo-, hydrochloride

Benzenemethanamine, 3-iodo-, hydrochloride (1:1)

3-iodo-Benzenemethanamine hydrochloride (1:1)

Trimethoprim Impurity 29

3-Iodo-benzenemethanamine HCl

3718-88-5

C7H9IN

C7H8INClH

C7H9ClIN

C7H8INHCl

C7H8NIxHCl2

Building Blocks

Amine Salts

Organic Building Blocks

Nitrogen Compounds

Anilines, Amides & Amines

Iodine Compounds

Anilines, Aromatic Amines and Nitro Compounds

Amine Salts

Nitrogen Compounds

Organic Building Blocks