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  • <img src="https://img-i-album.toocle.com/view/2023/04/20/28/64409c10ccf28.jpg" style="max-width:100%;"/>西瓜皮提取物以葫芦科植物西瓜的外层干燥果皮草为原料,经加热回流提取、减压浓缩、喷雾干燥而成的水溶性粉末状提取物产品,即保持了植物原有的有效成分,又使产品呈粉状,流动性好,易溶解,易保存。【产品名称】:西瓜皮提取物,西瓜皮精细粉末水提,西瓜皮粉可溶解,西瓜皮浸膏粉【植物来源】:葫芦科植物西瓜的外层干燥果皮草【别      名】:西瓜青、西瓜翠衣、西瓜翠【提取溶剂】:水【干燥方式】:喷雾干燥【产品含量】:10:1【产品性状】:水溶性棕色粉末【粒      度】:过80目筛网【检测方法】:TLC【应用范围】:保健、饮料、食品、化妆品、工业等领域【存储条件】:密封遮光,贮存在干燥、阴凉、通风良好的地方。【生产工艺】:原料—清洗—提取—浓缩—喷雾干燥—过筛—包装【包      装】:1kg、5kg、10kg、25kg定量包装或按要求包装【 保质期 】:两年【物流运输】:默认韵达快递,申通速运,如有其它请务必告知
  • <img src="https://img-i-album.toocle.com/view/2023/04/20/13/64409d0877f13.jpg" style="max-width:100%;"/>西番莲提取物以西番莲科植物西番莲的干燥全草为原料,经加热回流提取、减压浓缩、喷雾干燥而成,保有了原有的药材的有效成分,产品呈粉状,流动性好,口感佳,易溶解,易保存。【产品名称】:西番莲提取物,水溶性西番莲提取物,供应西番莲提取物浸膏【英文名称】:Artemisiae Argyi Folium【植物来源】:西番莲科植物西番莲的干燥全草【提取方式】:加热回流提取【提取溶剂】:水【干燥方式】:喷雾干燥【有效成分】:本品主要含白杨素、苯并二氮杂类化合物、新西兰鸡蛋果氰苷B-4-硫酸酯、牡荆素、导荭草素、芹菜素-8-C-双葡萄糖苷、焦性儿茶酚等成分【产品性状】:水溶性棕色粉末【粒      度】:过80目【检测方法】:TLC【存储条件】:密封遮光,贮存在干燥、阴凉、通风良好的地方。【生产工艺】:原料—清洗—提取—浓缩—喷雾干燥—过筛—包装【包      装】:25kg定量包装或按客户要求包装【 保质期 】:两年【物流运输】:默认韵达快递,申通速运,如有其它请务必告知!
  • 【英文名】:Amla extract拉丁名:Phyllanthus acidus【产品规格】:1.5% VC & 5%多酚【植物来源】:大戟科叶下珠属常绿灌木或小乔木的果实提取【提取部位】:果实【有效成分】:维生素Vitmin C,多酚【检测方法】:滴定【产品性状】:棕黄色粉末【包装】25公斤/桶(内包装为双层塑料袋,外用铝箔袋或纸板桶)【保存】置于阴凉干燥、避光,避高温处【保质期】:2年【质量指标】目数: 95%过80目干燥失重:≤5% 灰份:≤5%  重金属:≤20ppm 【微生物标准】细菌总数:≤1000/g   霉菌、酵母菌:≤100/g   【微生物标准】细菌总数:≤1000/g   霉菌、酵母菌:≤100/g  窗体顶端【产品简介】:西印度醋栗树是一种热带果树,喜温暖潮湿且全日照的环境,分布于热带及亚热带海拔900米以下地区。据说该树源自马达加斯加岛,被带到印度东部后再辗转至菲律宾及附近的海岛,那时并未被广泛栽培,后来在印度尼西亚、越南等地才渐渐的普遍起来,我国台湾省的嘉义农试所有引种。现在非洲的几内亚比绍在庭院、街道两旁也有栽培。
  • 主要功能: 巴西莓所含的主要有益物质包括多酚、黄酮类化合物,大部份是花色甙及原花色甙类。巴西莓的深紫色果皮所含的花色甙是红酒的很多倍,有强效的抗氧化作用,含有Omega 6(亚麻油酸)及Omega 9(油酸)这两种必须的脂肪酸。
  • 中文名称】:盐酸度洛西汀   【英文名称】:Duloxetine hydrochloride   【CAS   号】:136434-34-9   【分 子 式】:C18H20ClNOS   【分 子 量】:333.88   【含    量】:99%
  • Appearance White or almost white crystalline powder Identification Positive Melting point 191°C ~195°C Absorbance(E1cm) 465~495 Specific Rotation +288°~ +298° Heay Metals ≤20 ppm Residue Solvents ≤0.2% Loss on drying ≤0.5% Residue On Ignition ≤0.1% Assay 98.0%~102.0% Related Substances Total ≤1.5% Single ≤0.5%
  • Appearance White crystalline powder, odorless Solubility Freely soluble in anhydrous ethanol, soluble in methylene chloride Practically soluble in water Identification HPLC The appearance time of docetaxel is concordant with the appearance time form docetaxel standard IR The spectrum of docetaxel is concordant with the spectrum of obtain from docetaxel standard Clarity of the solution Solution S is not more intensely colored than reference suspension Ⅱ Color the solution Less than the reference solution B5 Specific rotation -38.5~-41.5° Related substance Impurity A≤0.2% Impurity B≤0.3% Impurity C≤0.15% Impurity E≤0.15% Other single impurity≤0.5% Sum of impurities ≤1.0% Dichloromethane ≤0.06% N-hexane ≤0.029% Ethyl acetate ≤0.5% Acetone ≤0.5% Methanol ≤0.3% Water ≤1.5% Sulphated ash ≤0.1% metals ≤20ppm Bacterial endotoxins <0.3IU/mg Assay 97.5~102.0%
  • Appearance A white or almost white powder Identification Complies with the infrared absorptions of RS Clarity and color of the solution Should be clear and colorless Loss on drying 1.0% max Residue on ignition 0.1% max metal 10ppm max Related substance Single impurity: 0.1% max Total impurity: 0.3% max Isopropanol 2000ppm max Methanol 1500ppm max Assay 98%-102%
  • Appearance White or almost white crystalline powder Identification (1),(2),(3) Appearance of solution 5# max Clear 1# max PH 8.0-10.0 Specific optical rotation +258˚ ~+287˚ Residual Solvents Comply with standard Related substance Comply with standard 2-ethylhexanoate 0.8% max Water 2.0% max Bacterial endotoxins 0.1IU/mg max Sterility Confirm Assay(on dry base) 85% min
  • Appearance White or pale yellow amorphous powder Solubility Practical insoluble in water,very soluble in ethanol(96%),slightly soluble in hexane Identification Conforms Appearance of solution Clear,color ≤GY5 Related Substances Method A Impurity A ≤1.5% Impurity B ≤0.5% Impurity C ≤1.5% Impurity D ≤2.5% Impurity E+F ≤1.7% Impurity G ≤1.5% Impurity L ≤0.5% Any other individual impurity before impurity G ≤0.5% Method B Impurity H+I ≤1.0% Impurity J ≤0.5% Impurity K ≤0.5% Any other individual impurity after impurity G ≤0.5% Total impurity ≤7.0% metals ≤ 20ppm Water ≤ 1.3% Sulphated Ash ≤0.2% Assay(on the anhydrous basis) 92.0%~~102.0% Antioxidant Assay 0.3%~~0.6% Residual Solvents Methanol ≤3000ppm Ethanol ≤5000ppm Dichloromethane ≤600ppm Propenol ≤50ppm Triethylamine ≤320ppm N-Heptane ≤5000ppm Methylcyclohexane ≤1180ppm 1,4-Dioxane ≤380 Butyl Ac3tate ≤5000ppm Dinethyl Sulfixide ≤5000ppm