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"hydrogen cyanide"¿¡ ´ëÇÑ °Ë»ö °á°úÀÔ´Ï´Ù. °Ë»ö °á°ú º¸´Â µµÁß¿¡ Tab ۸¦ ´©¸£½Ã¸é °Ë»ö âÀÌ ¼±Åõ˴ϴÙ.
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¿µ¹® pH, hydrogen ion concentration ÇÑ±Û ¼ö¼ÒÀ̿³óµµÁö¼ö
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  Ç÷¾×À̳ª ¼Òº¯¿¡¼­ ½Ç½ÃÇϴ °Ë»çÇ׸ñ. pH°Ë»ç´Â ÀÎüÀǠü¾×ÀÇ »ê¼º, ¾ËÄ®¸®¼ºÀ» ¾Ë¾Æº¸´Â Áß¿äÇÑ °Ë»çÀÌ´Ù. ÀÎü´Â ¾à¾ËÄ®¸®¼º¿¡ ¼ÓÇϳª, À̺¸´Ù pHÀÇ Áõ°¡³ª °¨¼Ò°¡ ³ªÅ¸³¯ °æ¿ì, »ý¸í¿¡ À§ÇèÀÌ ¹ß»ýÇÑ´Ù. ÀÎü³»¿¡´Â ÀÌ·± »êµµÀÇ Áõ°¨À» ¸·±âÀ§ÇØ, À̸¥¹Ù ¿ÏÃæÁ¦µéÀÌ ¸¹ÀÌ Á¸ÀçÇϸç, Æ¯È÷ ÇãÆÄ¿Í ÄáÆÏÀÌ ¿ÏÃæÀÛ¿ëÀ» ¼öÇàÇϴ ÁÖ¿ä±â°üÀÌ´Ù.
  
  ÄáÆÏÀº »êµµ°¡ ³ôÀ» °æ¿ì, ¼Òº¯¿¡¼­ »êµµ¸¦ Áõ°¡½ÃÄÑ ¹èÃâÇÔÀ¸·Î½á Ç÷¾×³»ÀÇ ¾ËÄ®¸®¼º ³óµµ°¡ Áõ°¡Çϵµ·Ï ÇÑ´Ù. ¶ÇÇÑ ÇãÆÄ¿¡¼­µµ, Ç÷¾×³»¿¡ »êµµ°¡ Áõ°¡½Ã È£ÈíÀ» Áõ°¡ÇÔÀ¸·Î½á ¹ÛÀ¸·Î »êÀÇ ¹èÃâÀ» Áõ°¡½ÃŲ´Ù. ÀÌ·± ÇãÆÄ¿Í ÄáÆÏÀÇ ±ÕÇüÀº ¾ÆÁÖ ÀûÀýÈ÷ ÀÌ·ç¾îÁö°í ÀÖÀ¸¸ç, ¾î´À ÇÑ ±â°üÀÇ ÀÌ»óÀÌ ¹ß»ýÇϸé, ÀÌ·± ±ÕÇüÀº ±ú¾îÁö±â ½±´Ù.
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  • ¿µ¹®
    ÇѱÛ
  • cyanide
    ½Ã¾ÈÈ­¹°
  • heavy hydrogen
    Áß¼ö¼Ò
  • hydrogen
    ¼ö¼Ò
  • hydrogen bond
    ¼ö¼Ò°áÇÕ
  • hydrogen disulfide
    ÀÌȲȭ¼ö¼Ò
  • hydrogen iodide
    ¿ä¿ÀµåÈ­¼ö¼Ò
  • hydrogen ion
    ¼ö¼ÒÀÌ¿Â
  • hydrogen ion concentration
    ¼ö¼ÒÀ̿³óµµ
  • hydrogen peroxide
    °ú»êÈ­¼ö¼Ò
  • hydrogen scale
    ¼ö¼Òôµµ
  • hydrogen selenide
    ¼¿·»È­¼ö¼Ò
  • hydrogen sulfide
    Ȳȭ¼ö¼Ò
  • light hydrogen
    °æ¼ö¼Ò
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  • ¿µ¹®
    ÇѱÛ
  • cyanide
    ½Ã¾ÈÈ­¹°
  • hydrogen
    ¼ö¼Ò
  • hydrogen peroxide
    °ú»êÈ­¼ö¼Ò
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  • ¿µ¹®
    ÇѱÛ
  • cyanide
    ½Ã¾ÈÈ­¹°
  • active hydrogen
    Ȱ¼º¼ö¼Ò
  • hydrogen bond
    ¼ö¼Ò°áÇÕ
  • hydrogen ion concentration
    ¼ö¼ÒÀ̿³óµµ
  • hydrogen flame detector
    ¼ö¼ÒºÒ²É°ËÃâ±â, ¼ö¼ÒÈ­¿°°ËÃâ±â
  • hydrogen exponent
    ¼ö¼ÒÁö¼ö
  • hydrogen ion exponent
    ¼ö¼ÒÀÌ¿ÂÁö¼ö
  • hydrogen
    ¼ö¼Ò
  • hydrogen disulfide
    ÀÌȲȭ¼ö¼Ò
  • hydrogen selenide
    ¼¿·»È­¼ö¼Ò
  • heavy hydrogen
    Áß¼ö¼Ò
  • hydrogen iodide
    ¿ä¿ÀµåÈ­¼ö¼Ò
  • hydrogen ion
    ¼ö¼ÒÀÌ¿Â
  • hydrogen peroxide
    °ú»êÈ­¼ö¼Ò
  • hydrogen scale
    ¼ö¼Òôµµ
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  • ¿µ¹®
    ÇѱÛ
  • hydrogen cyanide
    ½Ã¾ÈÈ­¼ö¼Ò.
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  • ¿µ¹®
    ÇѱÛ
  • potassium cyanide broth base
    û»êÄ®·ý¾×ü±âÃʹèÁö
  • H+ (Hydrogen ion)
    ¼ö¼ÒÀÌ¿Â
  • Hydrogen
    ¼ö¼Ò(â©áÈ)
  • Hydrogen balance
    ¼ö¼ÒÆòÇü(â©áÈøÁû¬)
  • Hydrogen bond
    ¼ö¼Ò°áÇÕ(â©áÈÌ¿ùê)
  • Hydrogen ion
    ¼ö¼ÒÀÌ¿Â
  • Hydrogen peroxide
    °ú»êÈ­¼ö¼Ò(Φ߫ûùâ©áÈ)
  • Hydrogen sulfide
    Ȳȭ¼ö¼Ò(üÜûùâ©áÈ)
  • Hydrogen-ATP ase mechanism
    ¼ö¼Ò-¾Æµ¥³ë½Å»ïÀλêÈ¿¼Ò ±âÀÛ
  • active hydrogen
    Ȱ¼º¼ö¼Ò(¡­â©áÈ).
  • heavy hydrogen =ducterium
    Áß¼ö¼Ò(ñìâ©áÈ).
  • hydrogen acceptor
    ¼ö¼Ò¼ö¿ëü.
  • hydrogen cycle
    ¼ö¼Òȯ(¡­ü»), ¼ö¼Ò°í¸®.
  • hydrogen disulfide
    ÀÌȲȭ¼ö¼Ò.
  • hydrogen donator
    ¼ö¼Ò°ø¿©Ã¼(¡­Íêæ¨ô÷).
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  • ¿µ¹®
    ÇѱÛ
  • hydrogen cyanide
    ½Ã¾ÈÈ­¼ö¼Ò.
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  • ¿µ¹®
    ÇѱÛ
  • ascorbate cyanide test
    ¾Æ½ºÄÚ¸£ºó»ê½Ã¾ÈÈ­¹°½ÃÇè
  • cacodyl cyanide
    ½Ã¾ÈÈ­Ä«ÄÚµô.
  • cadmium potassium cyanide
    ½Ã¾ÈÈ­Ä«µå¹Ì¿òÄ®·ý.
  • complex cyanide
    ½Ã¾ÈÈ­Âø¿°(¡­ûùó¹ç¤), ½Ã¾ÈÈ­º¹ÇÕ¹°.
  • cyanide
    ½Ã¾ÈÈ­¹°(¡­ûùÚª).
  • cyanide
    ½Ã¾ÈÈ­¹°
  • cyanide complex
    ½Ã¾ÈÈ­¹°º¹ÇÕü
  • cyanide goiter
    ½Ã¾È»ê¿° °©»ó¼±Á¾(¡­ß«ç¤Ë£ßÒàÍðþ).
  • cyanide poisoning
    ½Ã¾ÈÈ­¹°Áßµ¶
  • cyanide poisoning
    ½Ã¾È Áßµ¶(¡­ñéÔ¸)
  • cyanide process
    ½Ã¾ÈÈ­¹ý(¡­Ûö), ûȭ¹ý.
  • cyanide-nitroprusside test
    ½Ã¾ÈÈ­-³ªÀÌÆ®·ÎǪ¸£»çÀÌµå °Ë»ç
  • cyanide-nitroprusside test
    ½Ã¾ÈÈ­¹°-´ÏÆ®·ÎǪ¸£»çÀ̵å½ÃÇè
  • potassium cyanide broth base
    û»êÄ®·ý¾×ü±âÃʹèÁö
  • active hydrogen
    Ȱ¼º¼ö¼Ò(¡­â©áÈ).
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  • ¿µ¹®
    ÇѱÛ
  • cyanide
    ½Ã¾ÈÈ­¹°(ûùÚª)
  • cooperative hydrogen bonding
    Çùµ¿ ¼ö¼Ò°áÇÕ(úðÔÒâ©áÈÌ¿ùê)
  • heavy hydrogen
    Áß¼ö¼Ò(ñìâ©áÈ)
  • hydrogen
    ¼ö¼Ò(â©áÈ)
  • hydrogen bond
    ¼ö¼Ò °áÇÕ(â©áÈÌ¿ùê)
  • hydrogen carrier
    ¼ö¼Ò ¿î¹ÝÀÚ(â©áÈê¡Úæí­)
  • hydrogen electrode
    ¼ö¼Ò Àü±Ø(â©áÈï³Ð¿)
  • hydrogen exchange
    ¼ö¼Ò ±³È¯(â©áÈÎßüµ)
  • hydrogen ion concentration
    ¼ö¼Ò(â©áÈ)À̿ ³óµµ(ÒØÓø)
  • hydrogen ion euqilibrium
    ¼ö¼Ò(â©áÈ)À̿ ÆòÇü(øÁû¬)
  • hydrogen ion titration curve
    ¼ö¼Ò(â©áÈ)À̿ ÀûÁ¤°î¼±(îêïÒÍØàÊ)
  • hydrogen iostope exchange
    ¼ö¼Ò µ¿À§¿ø¼Ò ±³È¯(â©áÈÔÒêÈêªáÈÎßüµ)
  • hydrogen peroxide
    °ú»êÈ­ ¼ö¼Ò(Φ߫ûùâ©áÈ)
  • hydrogen transport system
    ¼ö¼Ò ¼ö¼Û(â©áÈâÃáê) ½Ã½ºÅÛ
  • tertiary hydrogen bonds
    »ïÂ÷¼ö¼Ò°áÇÕ (ß²ó­â©áÈ Ì¿ùê)
KI ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 2 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • hydrogen
    ¼ö¼Ò
  • hydrogen nucleus
    ¼ö¼ÒÇÙ
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
HCN Hydrogen Cyanide; û»ê
CCCP carbonyl cyanide m-chloro-phenyl-hydrazone
CN- cyanide anion
CYN cyanide
H2S Hydrogen Sulfate; Ȳȭ¼ö¼Ò
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
HCN Hydrogen cyanide
CCCP Carbonyl cyanide m-chloro-phenylhydrazone
CN Cyanide
KCN cyanide
FCCP of carbonyl cyanide p-trifluoromethoxy-phenylhydrazone
Çѱ¹Ç¥ÁØÁúº´»çÀκзù ¾àÀÚ ¸ÂÃã °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
  • ÄÚµå
    ¿µ¹®
    ÇѱÛ
  • T57.3
    Hydrogen cyanide
    ½Ã¾ÈÈ­¼ö¼Ò
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  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • hydrogen cyanide
    ½Ã¾ÈÈ­ ¼ö¼Ò
    ¹«»öÀÇ µ¶¼ºÀÌ °­ÇÑ ¾×ü³»Áö ±âü. »ì¼­Á¦, »ìÃæÁ¦·Î »ç¿ëµÈ´Ù.
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  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • ascorbate cyanide test
    ¾Æ½ºÄÚ¸£ºó»ê ½Ã¾ÈÈ­¹° ½ÃÇè
  • cacodyl cyanide
    ½Ã¾ÈÈ­Ä«ÄÚµô
  • cyanide
    »çÀ̾ÈÈ­¹°
    »çÀ̾ÈÀÇ ÀÌ¿øÈ­ÇÕ¹°.
  • cyanide-nitroprusside test
    ½Ã¾ÈÈ­-³ªÀÌÆ®·ÎǪ¸£»çÀÌµå °Ë»ç
  • active hydrogen
    Ȱ¼º ¼ö¼Ò
  • hydrogen acceptor
    ¼ö¼Ò ¼ö¿ëü
    ½Åü Á¶Á÷ Áß¿¡¼­ Çø±âÀûÀ¸·Î ÀϾ´Â »êÈ­ ȯ¿ø ¹ÝÀÀ¿¡¼­ ȯ¿øµÇ´Â ¹°Áú.
  • hydrogen bicarbonate

    hydrogen bond (¼ö¼Ò °áÇÕ

    1°³ÀÇ ºÐÀÚÀÇ °í¸³ ÀüÀÚ½Ö°ú ´Ù¸¥ ºÐÀÚÀÇ ¼ö¼Ò ¿øÀÚ°£¿¡ »ý¼ºµÇ´Â ½Ö±ØÀÚ Àη¿¡ ÀÇÇÑ 2Â÷ °áÇÕ.
  • hydrogen disulfide
    ÀÌȲȭ ¼ö¼Ò
  • hydrogen donor
    ¼ö¼Ò °ø¿©Ã¼
    ¼ö¼Ò¸¦ ´Ù¸¥ ¹°Áú¿¡ °ø¿©ÇÏ´Â ¹°Áú ¶Ç´Â È­ÇÕ¹°.
  • hydrogen fluoride
    ºÒÈ­ ¼ö¼Ò
  • hydrogen ion
    ¼ö¼Ò ÀÌ¿Â
    ¼ö¼Ò ¿øÀÚÀÇ ÇÙ ¶Ç´Â ÀüÀÚ¸¦ »ó½ÇÇÑ ¼ö¼Ò ¿øÀÚ. À̰ÍÀº ÀüÀÚÀÇ À½ ÀüÇÏ¿Í µ¿·®ÀÇ ¾ç ÀüÇϸ¦ °¡Áø´Ù.
  • hydrogen ion exchange
    ¼ö¼Ò À̿ ±³È¯
  • hydrogen nucleus
    ¼ö¼Ò ÇÙ
  • hydrogen peroxide solution
    °ú»êÈ­ ¼ö¼Ò¼ö
  • hydrogen sulfide
    Ȳȭ ¼ö¼Ò
    ºÒÄèÇÑ µ¶ °¡½º. È­ÇÐ ½Ã¾àÀ¸·Î »ç¿ëµÈ´Ù.
CancerWEB ¿µ¿µ ÀÇÇлçÀü ¸ÂÃã °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
hydrogen cyanide <chemical> Hydrogen cyanide (hcn). A toxic liquid or colourless gas. It is found in the smoke of various tobacco products and released by combustion of nitrogen-containing organic materials.
Pharmacological action: poisons.
Chemical name: Hydrocyanic acid
(12 Dec 1998)
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
allyl cyanide CH2==CHCH2CN; 3-butenenitrile;found in some mustard oils.
(05 Mar 2000)
ascorbate-cyanide test A test for glucose-6-phosphate-deficient red blood cells; blood is incubated with sodium cyanide and ascorbate; the hydrogen peroxide generated is free to oxidise haemoglobin to methemoglobin, since cyanide inhibits catalase; a brown colour is produced more rapidly in glucose 6-phosphate-deficient cells.
(05 Mar 2000)
carbonyl cyanide m-chlorophenyl hydrazone <chemical> A proton ionophore. It is commonly used as an uncoupling agent and inhibitor of photosynthesis because of its effects on mitochondrial and chloroplast membranes.
Pharmacological action: uncoupling agents, ionophores.
Chemical name: Propanedinitrile, ((3-chlorophenyl)hydrazono)-
(12 Dec 1998)
carbonyl cyanide p-trifluoromethoxyphenylhydrazone <chemical> A proton ionophore that is commonly used as an uncoupling agent in biochemical studies.
Pharmacological action: ionophores, uncoupling agents.
Chemical name: Propanedinitrile, ((4-(trifluoromethoxy)phenyl)hydrazono)-
(12 Dec 1998)
potassium cyanide <chemical> Potassium cyanide (k(cn)). A highly poisonous compound that is an inhibitor of many metabolic processes, but has been shown to be an especially potent inhibitor of haem enzymes and haemproteins. It is used in many industrial processes.
Pharmacological action: enzyme inhibitors, poisons.
Chemical name: Potassium cyanide (K(CN))
(12 Dec 1998)
cyanide 1. The radical -CN or ion (CN)-. The ion is extremely poisonous, forming hydrocyanic acid in water; inhibits respiratory proteins.
2. A salt of HCN or a cyano-containing molecule.
(05 Mar 2000)
cyanide dihydratase <enzyme> From bacillus pumilus c1; catalyses the conversion of cyanide to formate and ammonia
Registry number: EC 3.5.5.-
(26 Jun 1999)
cyanide hydratase <enzyme> Converts hcn to formamide in the fungus gloeocercospora sorghi
Registry number: EC 4.2.1.66
Synonym: formamide hydro-lyase
(26 Jun 1999)
cyanide methemoglobin A relatively nontoxic compound of cyanide with methemoglobin, which is formed when methylene blue is administered in cases of cyanide poisoning.
Synonym: cyanide methemoglobin.
(05 Mar 2000)
cyanide-nitroprusside test A qualitative test for diagnosis of cystinuria; the addition of fresh sodium cyanide formed by sodium nitroprusside to a sample of urine gives rise to a stable red-purple colour in the presence of cystine.
(05 Mar 2000)
cyanide poisoning A fairly common disease of herbivorous animals, but uncommon in man. Cyanogenic compounds are very toxic to humans either by inhalation or ingestion.
(27 Sep 1997)
sodium cyanide <chemical> Sodium cyanide (na(cn)). A highly poisonous compound that is an inhibitor of many metabolic processes and is used as a test reagent for the function of chemoreceptors. It is also used in many industrial processes.
Pharmacological action: enzyme inhibitors, indicators and reagents, poisons.
Chemical name: Sodium cyanide (Na(CN))
(12 Dec 1998)
thiosulfate cyanide transsulfurase <enzyme> An enzyme that catalyses the transfer of the planetary sulfur atom of thiosulfate ion to cyanide ion to form thiocyanate ion.
Chemical name: Thiosulfate:cyanide sulfurtransferase
Registry number: EC 2.8.1.1
(12 Dec 1998)
arseniureted hydrogen <chemistry> A compound of arsenic and hydrogen, AsH3, a colourless and exceedingly poisonous gas, having and odour like garlic; arseniureted hydrogen.
Origin: From Arsenic.
Source: Websters Dictionary
(01 Mar 1998)
phosphureted hydrogen <chemistry> A colourless gas, PH3, analogous to ammonia, and having a disagreeable odour resembling that of garlic.
Synonym: hydrogen phosphide, and formerly, phosphureted hydrogen.
It is the most important compound of phosphorus and hydrogen, and is produced by the action of caustic potash on phosphorus. It is spontaneously inflammable, owing to impurities, and in burning produces peculiar vortical rings of smoke.
Source: Websters Dictionary
(01 Mar 1998)
MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 1 ÆäÀÌÁö: 1
  • Hydrogen Cyanide - »õâ Hydrogen cyanide (HCN); A toxic liquid or colorless gas. It is found in the smoke of various tobacco products and released by combustion of nitrogen-containing organic materials.
    Synonyms : Zyklon B, Acid, Hydrocyanic, Cyanide, Hydrogen
¿ÜºÎ ¸µÅ© - Merriam-Webster's ÀÇÇлçÀü ¸ÂÃã °Ë»ö (https://www.merriam-webster.com) °á°ú: 1 ÆäÀÌÁö: 1
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hydrogen cyanide a highly poisonous gas or volatile liquid that smells like bitter almonds; becomes a gas at around 90 degree Fahrenheit and is most dangerous when inhaled; the anhydride of hydrocyanic acid; used in manufacturing
Ãâó: wordnet.princeton.edu/perl/webwn
hydrogen cyanide Hydrogen cyanide is a chemical compound with chemical formula H-C≡N. A solution of hydrogen cyanide in water is called hydrocyanic acid or prussic acid. Pure hydrogen cyanide is a colorless, very poisonous, and highly volatile liquid that boils slightly above room temperature at 26
Ãâó: en.wikipedia.org/wiki/Hydrogen_cyanide
hydrogen cyanide CAS Number: 74-90-8. A colorless gas with a faint, bitter, almond-like odor. It is used in electroplating and metallury, in the production of other chemicals, and in some cases, fumigation. Chemical formula = HCN. Molecular weight = 27.03 g/mol.
Ãâó: www.pca.state.mn.us/gloss/glossary.cfm
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  • ¿µ¹®
    ÇѱÛ
  • cyanide
    ½Ã¾È(û)È­¹°;û»ê¿°;û»êÄ®¸®(³ªÆ®·ý);½Ã¾ÈÀ¸·Î ó¸®ÇÏ´Ù
  • cyanide process
    ûȭ¹ý !
  • potassium cyanide
    û»êÄ®¸®
  • hydrogen
    ¼ö¼Ò
  • heavy hydrogen
    Áß¼ö¼Ò
  • hydrogen
    ¼ö¼Ò (±âÈ£ H)
  • hydrogen bomb
    ¼ö¼ÒÆøÅº
  • hydrogen chloride
    ¿°È­ ¼ö¼Ò
  • hydrogen corona
    ¼ö¼Ò Äڷγª(Çý¼ºÀÇ ´ë±â ¿ÜÃø¿¡ Á¸ÀçÇÏ´Â °Å´ëÇÑ ¼ö¼Ò °¡½ºÀÇ ±¸¸§)
  • hydrogen ion
    ¼ö¼ÒÀÌ¿Â
  • hydrogen peroxide
    °ú»êÈ­¼ö¼Ò
  • hydrogen sulfide
    Ȳȭ¼ö¼Ò
  • hydrogen warhead
    ¼öÆø źµÎ
WordNet ÀÏ¹Ý ¿µ¿µ »çÀü °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
hydrogen cyanide a weak poisonous acid (HCN) used in fumigating and in synthesis of organic compounds
¿ÜºÎ ¸µÅ© - American Heritage Dictionary ¿µ¿µ»çÀü ¸ÂÃã °Ë»ö (https://www.ahdictionary.com) °á°ú: 1 ÆäÀÌÁö: 1
ÀÌ ¾Æ·¡ ºÎÅÍ´Â °á°ú°¡ ¾ø½À´Ï´Ù.
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  • Á¦Ç°¸í
    ¼ººÐ/ÇÔ·®
    ±¸ºÐ/º¸Çè±Þ¿©
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    ÇѱÛ
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  • ¿µ¹®
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