購物車 
-
N-BOC-6-溴代己胺
- names：
Boc-NH-C6-Br
- CAS號：
142356-33-0
MDL Number： MFCD06201019 - MF(分子式)： C11H22BrNO2 MW(分子量)： 280.2
- EINECS: Reaxys Number:
- Pubchem ID:16211353 Brand:BIOFOUNT
| 貨品編碼 | 規(guī)格 | 純度 | 價格 (￥) | 現(xiàn)價(￥) | 特價(￥) | 庫存描述 | 數(shù)量 | 總計 (￥) |
|---|---|---|---|---|---|---|---|---|
| YZM000952-5g | 5g | 97% | ￥ 1280.00 | ￥ 1280.00 | 2-3days | ￥ 0.00 | ||
| YZM000952-1g | 1g | 97% | ￥ 320.00 | ￥ 320.00 | 2-3days | ￥ 0.00 | ||
| YZM000952-250mg | 250mg | 97% | ￥ 168.00 | ￥ 168.00 | 2-3days | ￥ 0.00 |
| 中文別名 | N-BOC-6-溴代己胺(142356-33-0,Boc-NH-C6-Br);6-(BOC-氨基)溴己烷;N-(6-溴己基)氨基甲酸叔丁酯;(6-溴己基)氨基甲酸 叔丁酯 |
| 英文別名 | Boc-NH-C6-Br(142356-33-0);6-(Boc-amino)hexyl bromide;N-Boc-6-Bromo-hexylamine |
| CAS號 | 142356-33-0 |
| Inchi | InChI=1S/C11H22BrNO2/c1-11(2,3)15-10(14)13-9-7-5-4-6-8-12/h4-9H2,1-3H3,(H,13,14) |
| InchiKey | NXQXVXILNVTMNA-UHFFFAOYSA-N |
| 分子式 Formula | C11H22BrNO2 |
| 分子量 Molecular Weight | 280.2 |
| 溶解度Solubility | |
| 性狀 | 無色至淺黃色液體 |
| 儲藏條件 Storage conditions | storage at -4℃ (1-2weeks), longer storage period at -20℃ (1-2years) |
N-BOC-6-溴代己胺(142356-33-0,Boc-NH-C6-Br)實驗注意事項：
1.實驗前需戴好防護眼鏡，穿戴防護服和口罩，佩戴手套，避免與皮膚接觸。
2.實驗過程中如遇到有毒或者刺激性物質(zhì)及有害物質(zhì)產(chǎn)生，必要時實驗操作需要手套箱內(nèi)完成以免對實驗人員造成傷害
3.實驗后產(chǎn)生的廢棄物需分類存儲，并交于專業(yè)生物廢氣物處理公司處理，以免造成環(huán)境污染
N-BOC-6-溴代己胺(142356-33-0,Boc-NH-C6-Br) Experimental considerations:
1. Wear protective glasses, protective clothing and masks, gloves, and avoid contact with the skin during the experiment.
2. The waste generated after the experiment needs to be stored separately, and handed over to a professional biological waste gas treatment company to avoid environmental pollution.
Tag:N-BOC-6-溴代己胺(142356-33-0,Boc-NH-C6-Br),N-BOC-6-溴代己胺試劑,N-BOC-6-溴代己胺的純度,N-BOC-6-溴代己胺的作用,N-BOC-6-溴代己胺的外觀,N-BOC-6-溴代己胺的合成路線,N-BOC-6-溴代己胺的廠家,N-BOC-6-溴代己胺的MSDS,N-BOC-6-溴代己胺的價格
| 產(chǎn)品說明 | N-BOC-6-溴代己胺(142356-33-0,Boc-NH-C6-Br)是用于抗體-藥物偶聯(lián)物（ADC）的可裂解linker。 |
| Introduction | Boc-NH-C6-Br (142356-33-0,N-BOC-6-溴代己胺) is a cleavable linker for antibody-drug conjugates (ADC). |
| Application1 | |
| Application2 | |
| Application3 |
| 警示圖 | |
| 危險性 | warning |
| 危險性警示 | Not available |
| 安全聲明 | H303吞入可能有害+H313皮膚接觸可能有害+H2413吸入可能對身體有害 |
| 安全防護 | P264處理后徹底清洗+P280戴防護手套/穿防護服/戴防護眼罩/戴防護面具+P305如果進入眼睛+P351用水小心沖洗幾分鐘+P338取出隱形眼鏡（如果有）并且易于操作,繼續(xù)沖洗+P337如果眼睛刺激持續(xù)+P2393獲得醫(yī)療建議/護理 |
| 備注 | 實驗過程中防止吸入、食入，做好安全防護 |
| 象形圖 |  |
|---|---|
| 信號警告 | Danger |
| GHS危險說明 |
Aggregated GHS information provided by 2 companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies. H314 (50%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation] H318 (50%): Causes serious eye damage [Danger Serious eye damage/eye irritation] Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown. |
| 防范說明代碼 |
P260, P264, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P363, P405, and P501 (The corresponding statement to each P-code can be found at the GHS Classification page.) |
| Glucose-Responsive Insulin Delivery by Microneedle-Array Patches Loaded with Hypoxia-Sensitive Vesicles(Biomedical Nanotechnology,2017) |
| Synthesis of Peptidomimics Through Sugar-Based Scaffolds(Peptidomimetics Protocols,1999) |
| High-performance liquid chromatographic assay with fluorescence detection for the evaluation of inhibitors against fatty acid amide hydrolase |
| Oral delivery of insulin with intelligent glucose-responsive switch for blood glucose regulation(Journal of Nanobiotechnology,2020) |
| Phage-guided modulation of the gut microbiota of mouse models of colorectal cancer augments their responses to chemotherapy(Nature Biomedical Engineering,2019) |
1.Synthesis of Peptidomimics Through Sugar-Based Scaffolds
Yves Le Merrer, Lydie Poitout, Jean-Claude Depezay
Poor oral bioavailability, low metabolic stability towards proteolysis and rapid excretion via both liver and kidneys displayed by innumerable peptides of potential therapeutic value has generated an intensive search for peptidomimics. A possible approach of such nonpeptidal peptidomimics is to replace the peptide by a scaffold that distributes in the space the peptidal side chains of amino acids essential for biological activity and mimics the bioactive conformation of the peptide.
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