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飼料添加劑 維生素A乙酸酯微粒檢測項目報價???解決方案???檢測周期???樣品要求? |
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本標準規(guī)定了飼料添加劑維生素A乙酸酯微粒的范圍、要求、試驗方法、驗收規(guī)則、標簽以及包裝運輸和儲存。 本標準適用于由合成維生素A乙酸酯,加入適量抗氧劑,采用明膠為主要輔料制成的微粒。
本文件規(guī)定了飼料添加劑β,β-胡蘿卜素-4,4-二酮(斑蝥黃)產品的技術要求、取樣、檢驗規(guī)則、標簽、包裝、運輸、貯存和保質期,描述了試驗方法。本文件適用于以維生素A乙酸酯或β-胡蘿卜素為主要原料,經化學合成制得的飼料添加劑β,β-胡蘿卜素-4,4-二酮(斑蝥黃)96型;以及以96型產品為原料,經二氯甲烷溶解,加入飼料原料明膠或淀粉或飼料添加劑木質素磺酸鹽等,噴霧干燥制得的飼料添加劑β,β-胡蘿卜素-4,4-二酮(斑蝥黃)10型。
本標準規(guī)定了飼料添加劑維生素AD<下標3>微粒的產品規(guī)格、技術要求、試驗方法、檢驗規(guī)則及其標簽、包裝、運輸和貯存。本標準適用于以飼料添加劑維生素A乙酸酯與維生素D<下標3>油為原料,配以一定量的乙氧喹啉及(或)2,6-二叔丁基-4-甲基苯酚(BHT)等抗氧化劑,采用明膠和淀粉等輔料,經噴霧法制成的微粒。本品在飼料工業(yè)中作為維生素類飼料添加劑。
本標準規(guī)定了飼料添加劑維生素D<下標3>(微粒)產品的要求、試驗方法、檢驗規(guī)則、標簽、包裝、運輸、貯存和保質期。本標準適用于以飼料添加劑維生素D<下標3>油為原料,配以一定量的抗氧化劑,采用明膠、淀粉等輔料制成的普通型飼料添加劑維生素D<下標3>(微粒)和采用麥芽糊精、乳化劑等輔料制成的水分散型飼料添加劑維生素D<下標3>(微粒)。輔料應符合《飼料原料目錄》《飼料添加劑品種目錄》以及《飼料衛(wèi)生標準》的規(guī)定?;瘜W名稱:(3β,5Z,7E)-9,10-開環(huán)膽甾-5,7,10(19)-三烯-3-醇分子式:C<下標27>H<下標44>O相對分子質量:384.64(2007年相對原子質量)
本標準規(guī)定了飼料添加劑80%核黃素(維生素B<下標 2>)微粒產品的要求、試驗方法、檢驗規(guī)則、標簽、包裝、運輸和貯存。本標準適用于生物發(fā)酵法制得的80%核黃素(維生素B<下標 2>)微粒,在飼料工業(yè)中作為維生素類飼料添加劑。
本標準規(guī)定了水產養(yǎng)殖的基本術語及其定義。本標準適用于水產養(yǎng)殖基本術語和基本概念的統(tǒng)一理解與使用。
本標準規(guī)定了飼料添加劑維生素A棕櫚酸酯(粉)產品的要求、試驗方法、檢驗規(guī)則以及標簽、包裝、運輸、貯存和保質期。本標準適用于以化學合成的維生素A棕櫚酸酯為原料,以變性淀粉等為輔料,加入適量抗氧劑,以噴霧法工藝生產的飼料添加劑維生素A棕櫚酸酯(粉)?;瘜W名稱:3,7-二甲基-9-(2,6,6-三甲基-1-環(huán)己烯-1-基)-2,4,6,8-壬四烯-1-棕櫚酸酯分子式:C<下標36>H<下標60>O<下標2>相對分子質量:524.86(2007年相對原子質量)
本標準規(guī)定了飼料添加劑10%蝦青素的范圍、要求、試驗方法、檢驗規(guī)則、標簽、包裝、運輸、貯存及保質期。本標準適用于以含量不低于96%的合成蝦青素為主要原料,以淀粉、明膠、蔗糖等為輔料,以噴霧法工藝生產的10%蝦青素。
本標準規(guī)定了飼料添加劑半胱胺鹽酸鹽β環(huán)糊精微粒的要求、試驗方法、檢驗規(guī)則及標簽、包裝、運輸、貯存和保質期的要求。本標準適用于以飼料級半胱胺鹽酸鹽為原料,經β環(huán)糊精包被,采用淀粉等為輔料制成的微粒。
本標準規(guī)定了飼料添加劑維生素D<下標 3>油產品的要求、試驗方法、檢驗規(guī)則及標簽、包裝、貯存、運輸。 本標準適用于由維生素D<下標 3>溶于符合飼料衛(wèi)生要求的植物油中,含有適量的穩(wěn)定劑如抗氧化劑等,用于制備飼料添加劑維生素D<下標 3>微粒,其維生素D<下標 3>含量不得低于50萬IU/g,制得的維生素D<下標 3>油。 化學名稱:膽鈣化醇 分子式:C<下標 27>H<下標 44>O 相對分子質量:384.6(2001年相對原子質量)。
本標準規(guī)定了食品企業(yè)對能源管理體系的認證要求。本標準適用于食品企業(yè)的能源管理體系認證,可用于食品企業(yè)建立、實施、保持和改進能源管理體系,也可作為各相關方考核評價食品企業(yè)能源管理體系的依據。
This International Standard specifies guidelines for the preparation of test samples from laboratory samples of animal feeding stuffs including pet foods. The guidelines mostly derive from those developed by AAFCO. The guidelines are overruled by special instructions and regulations for sample preparation demanded by specific analysis methods. Such analysis methods are developed by ISO and CEN. This international Standard does not include special guidelines for sample preparation for microbiological analysis of microorganisms like yeasts, bacteria and moulds. Nonetheless, for microorganisms which are used as feed additives (probiotics), some important aspects of sample preparation are addressed.
This standard specifies requirements for vascular device-drug combination products (VDDCPs) based upon current technical and medical knowledge. VDDCPs are medical devices with various clinical indications for use in the human vascular blood system. A VDDCP incorporates, as an integral part, substance(s) which, if used separately, can be considered to be a medicinal product (drug product) but the action of the medicinal substance is ancillary to that of the device and supports the primary mode of action of the device. With regard to safety, this Standard outlines requirements for intended performance, design attributes, materials, design evaluation, manufacturing, sterilization, packaging, and information supplied by the manufacturer. For implanted products, this standard should be considered as a supplement to ISO 14630, which specifies general requirements for the performance of non-active surgical implants. This standard should also be considered as a supplement to relevant device-specific standards, such as the ISO 25539 series specifying requirements for endovascular devices. Requirements listed in this standard also address VDDCPs that are not necessarily permanent implants.
This European Standard defines general rules for the enumeration of probiotic pediococci in feed samples(additives, premixtures and feeding stuffs) that contain pediococci as a single bacterial component or in amixture with other microorganisms. This standard is not applicable for mineral feeds which are defined ascomplementary feeding stuffs composed mainly of minerals and containing at least 40% crude ash (CouncilDirective 79/373/EEC) [3].There are different categories of feed samples:a) Additives containing about 1010 (colony forming units) CFU/gb) Premixtures containing about 108 CFU/gc) Feeds, meal or pellets, which contain about 106 CFU/g and include complete feeding stuffs, and milkreplacers.The detection limit is as defined in EN ISO 7218.
This European Standard defines general rules for the enumeration of probiotic lactobacilli in feed samples(additives, premixtures and feeding stuffs) that contain lactobacilli as a single bacterial component or in amixture with other microorganisms. This standard is not applicable to mineral feeds, which are defined ascomplementary feeding stuffs composed mainly of minerals and containing at least 40% crude ash (CouncilDirective 79/373/EEC [3]).There are different categories of feed samples:a) Additives containing about 10<(UP)10> colony forming units (CFU)/g;b) Premixtures containing about 10<(UP)8> CFU/g;c) Feeds, meal or pellets, which contain about 10<(UP)6> CFU/g and include complete feeding stuffs and milkreplacers.The detection limit is as defined in EN ISO 7218.