N-(tert-Butoxycarbonyl)glycine-15N, Glycine-15N, N-t-Boc derivative
BOC-[15N]GLY-OH
CAS: 106665-75-2
Molecular Formula: C7H13NO4
N-(tert-Butoxycarbonyl)glycine-15N, Glycine-15N, N-t-Boc derivative - Names and Identifiers
N-(tert-Butoxycarbonyl)glycine-15N, Glycine-15N, N-t-Boc derivative - Physico-chemical Properties
| Molecular Formula | C7H13NO4 |
| Molar Mass | 176.19 |
| Melting Point | 86-89 °C (lit.) |
| Storage Condition | -15°C |
N-(tert-Butoxycarbonyl)glycine-15N, Glycine-15N, N-t-Boc derivative - Risk and Safety
| Hazard Symbols | Xn - Harmful |
| Risk Codes | R22 - Harmful if swallowed R41 - Risk of serious damage to eyes |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. |
| UN IDs | UN 2811 6.1 / PGIII |
| WGK Germany | 3 |
N-(tert-Butoxycarbonyl)glycine-15N, Glycine-15N, N-t-Boc derivative - Introduction
BOC-[15N]GLY-OH is a compound which is a 15 nitrogen labeled Boc protected glycine (Gly) Ester. The following is a description of the nature, use, preparation and safety information of BOC-[15N]GLY-OH:
Nature:
BOC-[15N]GLY-OH is a white solid powder, stable at room temperature. It has good solubility and is soluble in organic solvents such as dimethyl sulfoxide (DMSO), dichloromethane (DCM) and dimethylformamide (DMF).
Use:
BOC-[15N]GLY-OH is often used as a labeling reagent in biochemical research and can be used to synthesize 15n-labeled polypeptides, proteins and other organic molecules. This 15 nitrogen labeled compound has a wide range of applications in nuclear magnetic resonance (NMR) spectroscopy.
Preparation Method:
The preparation of BOC-[15N]GLY-OH is usually carried out by labeling the existing Boc-protected glycine (BOC-GLY-OH). During the synthesis, the reactant with the 15 nitrogen is used in the amination reaction, and then the protecting group is removed to give the BOC-[15N]GLY-OH.
Safety Information:
BOC-[15N] The GLY-OH is not currently reporting toxic or hazardous. However, as a laboratory reagent, use is subject to safe chemical laboratory practices and appropriate personal protective equipment, such as lab gloves and goggles. In addition, it should be stored in a dry, cool place, away from fire and flammable substances. In case of any accident or discomfort, you should seek medical advice immediately.
Nature:
BOC-[15N]GLY-OH is a white solid powder, stable at room temperature. It has good solubility and is soluble in organic solvents such as dimethyl sulfoxide (DMSO), dichloromethane (DCM) and dimethylformamide (DMF).
Use:
BOC-[15N]GLY-OH is often used as a labeling reagent in biochemical research and can be used to synthesize 15n-labeled polypeptides, proteins and other organic molecules. This 15 nitrogen labeled compound has a wide range of applications in nuclear magnetic resonance (NMR) spectroscopy.
Preparation Method:
The preparation of BOC-[15N]GLY-OH is usually carried out by labeling the existing Boc-protected glycine (BOC-GLY-OH). During the synthesis, the reactant with the 15 nitrogen is used in the amination reaction, and then the protecting group is removed to give the BOC-[15N]GLY-OH.
Safety Information:
BOC-[15N] The GLY-OH is not currently reporting toxic or hazardous. However, as a laboratory reagent, use is subject to safe chemical laboratory practices and appropriate personal protective equipment, such as lab gloves and goggles. In addition, it should be stored in a dry, cool place, away from fire and flammable substances. In case of any accident or discomfort, you should seek medical advice immediately.
Last Update：2024-04-09 20:52:54
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View History
N-(tert-Butoxycarbonyl)glycine-15N, Glycine-15N, N-t-Boc derivative
Cyclohexanamine, 1-(1H-pyrrolo[3,2-b]pyridin-6-yl)-
2-(tetrapropenyl)succinic acid, monoester with propane-1,2-diol
4-chloro-3-[(2,4-dimethylphenyl)sulfamoyl]benzoic acid
(3-bromo-5-(tert-butyl)phenyl)methanol
3-氯甲基-5-(3,5-二甲基异恶唑-4-基)-1,2,4-氧二唑
4,4,6,8-tetramethyl-5H-dithiolo[5,4-c]quinoline-1-thione
2-Propenoic acid, 2-methyl-, methyl ester, polymer with butyl 2-propenoate and ethenylbenzene
Cyclohexanamine, 1-(1H-pyrrolo[3,2-b]pyridin-6-yl)-
2-(tetrapropenyl)succinic acid, monoester with propane-1,2-diol
4-chloro-3-[(2,4-dimethylphenyl)sulfamoyl]benzoic acid
(3-bromo-5-(tert-butyl)phenyl)methanol
3-氯甲基-5-(3,5-二甲基异恶唑-4-基)-1,2,4-氧二唑
4,4,6,8-tetramethyl-5H-dithiolo[5,4-c]quinoline-1-thione
2-Propenoic acid, 2-methyl-, methyl ester, polymer with butyl 2-propenoate and ethenylbenzene