Nα-Boc-L-arginine
Boc-L-Arg-OH.HCl
CAS: 35897-34-8
Molecular Formula: C11H23ClN4O4
Nα-Boc-L-arginine - Names and Identifiers
| Name | Boc-L-Arg-OH.HCl |
| Synonyms | HCl Boc-Arg-OH,HCl Boc-Arg-OH.HCl Boc-Arg-OH·HCl Boc-L-Arg-OH.HCl Nα-Boc-L-arginine Boc-L-Arginine HCL Boc-L-Arg-OH*H2O*HCl N-Boc-D-Arginine Hydrochloride tert-butyloxycarbonyl-arginine BOC-L-ARGININE HYDROCHLORIDE H20 Nα-(tert-Butoxycarbonyl)-L-arginine tert-butyloxycarbonyl-arginine hydrochloride N-.ALPHA.-BOC-L-ARGININE HYDROCHLORIDE MONOHYDRATE BOC-ARG-OH.HCLN-ALPHA BOC-L ARGININE HYDRO CHLORIDE N~2~-(tert-butoxycarbonyl)-N~5~-(diaminomethylidene)ornithine N-ALPHA-T-BUTYLOXYCARBONYL-L-ARGININE MONOHYDRATE HYDROCHLORIDE Nalpha-(tert-Butoxycarbonyl)-L-arginine Hydrochloride Monohydrate N~2~-(tert-butoxycarbonyl)-N~5~-(diaminomethylidene)-L-ornithine hydrochloride |
| CAS | 35897-34-8 |
| EINECS | 609-191-0 |
| InChI | InChI=1/C11H22N4O4.ClH/c1-11(2,3)19-10(18)15-7(8(16)17)5-4-6-14-9(12)13;/h7H,4-6H2,1-3H3,(H,15,18)(H,16,17)(H4,12,13,14);1H/t7-;/m0./s1 |
Nα-Boc-L-arginine - Physico-chemical Properties
| Molecular Formula | C11H23ClN4O4 |
| Molar Mass | 310.78 |
| Melting Point | >109oC (subl.) |
| Boling Point | 494°C at 760 mmHg |
| Flash Point | >230°F |
| Water Solubility | Slightly soluble in water. |
| Solubility | Acetic Acid (Sparingly), DMSO (Slightly), Methanol (Slightly), Water (Slightly) |
| Vapor Presure | 4.17E-11mmHg at 25°C |
| Appearance | White powder |
| Color | White |
| Storage Condition | Keep in dark place,Sealed in dry,Room Temperature |
| Refractive Index | -8 ° (C=2, H2O) |
| MDL | MFCD00063594 |
Nα-Boc-L-arginine - Risk and Safety
| Safety Description | S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes. |
| WGK Germany | 3 |
| HS Code | 29252900 |
| Hazard Class | IRRITANT |
Nα-Boc-L-arginine - Introduction
Boc-L-Arg-OH.HCl(Boc-L-Arg-OH.HCl) is an organic compound with the following properties:
1. appearance: white solid powder.
2. Solubility: Soluble in water and organic solvents such as methanol, ethanol, etc.
3. Stability: It is relatively stable at room temperature, but it is easy to absorb moisture when exposed to moisture or moisture.
Boc-L-Arg-OH.HCl have the following uses in chemical research and synthesis:
1. biological activity research: as a synthetic intermediate of peptide and protein, it is used to construct peptide chain.
2. drug research: for the synthesis of bioactive peptide drugs and antibiotics.
3. chemical analysis: used as a standard for mass spectrometry analysis.
The method of preparing Boc-L-Arg-OH.HCl mainly includes the following steps:
1. tert-Butyloxycarbonylation: L-arginine is reacted with tert-butyloxycarbonyl chloride (Boc-Cl) under alkaline conditions to obtain tert-butoxycarbonyl-L-arginine.
2. Hydrochloride salt formation: tert-Butoxycarbonyl-L-arginine was reacted with hydrochloric acid to obtain a Boc-L-Arg-OH.HCl.
Regarding safety information, Boc-L-Arg-OH.HCl it is relatively safe under normal use conditions, the following matters still need to be paid attention:
1. Avoid inhaling dust or skin contact: Wear protective gloves, glasses and masks to avoid direct contact or inhalation of dust.
2. storage precautions: should be stored in a dry, cool, well-ventilated place, avoid direct sunlight.
3. Disposal of waste: Waste should be properly disposed of in accordance with local regulations and can be disposed of through chemical waste treatment systems.
1. appearance: white solid powder.
2. Solubility: Soluble in water and organic solvents such as methanol, ethanol, etc.
3. Stability: It is relatively stable at room temperature, but it is easy to absorb moisture when exposed to moisture or moisture.
Boc-L-Arg-OH.HCl have the following uses in chemical research and synthesis:
1. biological activity research: as a synthetic intermediate of peptide and protein, it is used to construct peptide chain.
2. drug research: for the synthesis of bioactive peptide drugs and antibiotics.
3. chemical analysis: used as a standard for mass spectrometry analysis.
The method of preparing Boc-L-Arg-OH.HCl mainly includes the following steps:
1. tert-Butyloxycarbonylation: L-arginine is reacted with tert-butyloxycarbonyl chloride (Boc-Cl) under alkaline conditions to obtain tert-butoxycarbonyl-L-arginine.
2. Hydrochloride salt formation: tert-Butoxycarbonyl-L-arginine was reacted with hydrochloric acid to obtain a Boc-L-Arg-OH.HCl.
Regarding safety information, Boc-L-Arg-OH.HCl it is relatively safe under normal use conditions, the following matters still need to be paid attention:
1. Avoid inhaling dust or skin contact: Wear protective gloves, glasses and masks to avoid direct contact or inhalation of dust.
2. storage precautions: should be stored in a dry, cool, well-ventilated place, avoid direct sunlight.
3. Disposal of waste: Waste should be properly disposed of in accordance with local regulations and can be disposed of through chemical waste treatment systems.
Last Update：2024-04-09 21:21:28
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Spot supply
Product Name: Boc-Arg-OH hydrochloride Visit Supplier Webpage Request for quotationCAS: 35897-34-8
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
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