¼­ºñ½º¾È³» ȸ¿ø°¡ÀÔ È¸¿øÅ»Åð Áñ°Üã±âµî·Ï
Home Products Company Directory Trade ÇÑÁßÇÕÀÛ Áß±¹ÅõÀÚ
My ChemNet
   ÇöÀçÀ§Ä¡ : Home > Trade
¡¡
¿ÀÆÛ°Ô½ÃÆÇ
Offer to Buy
Offer to Sell







ÀÔ·ÂÀÏÀÚ: 2015-02-10
À¯È¿ÀÏÀÚ: 315-30-0

Á¦¸ñ: Allopurinol
  »óǰºÐ·ù: È­Çкñ·á¿Í ³ó¾à
  µî·ÏºÐ·ù: Offer to Sell
  ³»¿ë: Allopurinol Synonyms: TIMTEC-BB SBB004202;ISOPURINOL;LABOTEST-BB LT00244764;HPP;1H-PYRAZOLO[3,4-D]PYRIMIDIN-4-OL;AKOS BBS-00005290;ALLPURINOL;AKOS BBS-00002073 CAS: 315-30-0 MF: C5H4N4O MW: 136.11 EINECS: 206-250-9 Chemical Properties White to Off-White Solid Usage Xanthine oxidase inhibitor; decreases uric acid production. Used in treatment of hyperuricemia and chronic gout. Antiurolithic Usage antihyperuricemia, antigout, antiurolithic General Description Odorless tasteless white microcrystalline powder. Air & Water Reactions Insoluble in water. Reactivity Profile Allopurinol is an aminoalcohol. Amines are chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides. Allopurinol darkens above 572¡Æ F, and at an indefinite high temperature, Allopurinol chars and decomposes. At 221¡Æ F, maximum stability occurs at pH 3.1- 3.4. Allopurinol decomposes in acidic and basic solutions. Fire Hazard Flash point data for Allopurinol are not available; however, Allopurinol is probably combustible.

¿¬¶ôó
´ã ´ç ÀÚ:
Ivy Young
ȸ»çÁÖ¼Ò:
No 496 Zhongshan Road, Wuhan City, Hubei Province, China 430064
¿ìÆí¹øÈ£:
430064
ÀüÈ­¹øÈ£:
86-027-50755963
ÆÑ½º¹øÈ£:
86-027-50755963 
E - mail:
ycwlb045@yccreate.com

Copyright © 2003-2015 ChemNet.com All Right Reserved.