(Erlenmeyer flask) 100 ml3 ι(drip  tube;dropper)2
(graduated cylinder)10ml1  ߼ӱ߽(stir)
(õ)У׼У׼ universal calibration function or curve [of  separation]
()ѭϴ recycling  elution
ɫ2  ϴҺ
0.1g pan ̶ָȱpointer and  scale
1   ġУ
100 ml3 ֶ(straws) 25  ml1
250 ml3 ľԹܼ(test tube clamp;test tube  holder)1
50 ml2 10  ml1
50 ml4 ϴ(ear wadhing  bulb)
abatement 1:  2
ablution 1:ϴ  2ϴҺ
abnormal distribution  1:ֲ̬
above proof  ׼
above-critical  ٽϵģ
abrasive  1ĥϣĥ
abrupt change   2ζͻԾ
absolute calibration curve method  У׼߷
absolute deviation  ƫ
absolute error  
absolute ethyl alcohol  ˮҴ
absolute humidity  ʪȣ
absolute isotopic abundance measurement  ͬλطȲ
absolute manometer  ѹƣ
absolute mobility  ʶȣ
absolute precision  Ծܶȣ
absolute refractive index  ʣ
absolute retention time  Աʱ䣻
absolute sensitivity  ȣ
absolute stability constant  ȶ
absolute temperature  ¶ȣ
absolution configuration  Թͣ
absorbance  նȣȣ
absorbance index absorptivity 1ϵ  2ϵ
absorbance ratio  ȱֵ
absorbed dose  ռ
absorbed layer  ղ㣻
absorbent  ռյģģ
absorbing band  մ
absorption  գ
absorption chamber  ң
absorption factor  ʣ
absorption index  ָ
absorption peak  շ壻
absorption power  
absorption region  շΧ
absorption spectroscopy  չ׷
absorption spectrum  չף
absorption tube support  չܼܣ
absorption value  ֵ
abundance  ȣ
abundance of element  Ԫطȣ
accelerator  ӣ
acceptable life  Чʹ
acceptance level  ձ׼
acceptance quality level  AQLϸ׼
accessory substance  
accidental error  żȻ
accommodation  ڣ
accuracy  ׼ȷȣ
acetaldehyde  ȩ
acetic acid  ᣻
acetic anhydride  
acetoacetic ester  
acetone  ͪ
acetone titration  ͪζ
acetyl group  
acetylation  
acetylene  Ȳ
acetylenic bond  Ȳ
achiral molecule  Էӣ
acid degree  ȣ
acid dissociation constant  ⳣ
acidate  ữ
acidbase equilibrium  ƽ⣬
acidic  ʽԵģ
acidic solvent  ܼ
acidity  ȣ
acidometeracidimeter  ȼƣ
acticarbon  ̿
activate  ʹԣ
activated state  ̬
activating  
activating agent  
activator  
active center  ģ
active group  Իţ
active mass  Ч
active site  Ե㣻
actual column plate  ʵ
adapter tube  ӹܣ
additional peak  ӷ壻
additivity  Ӻԣ
adjacent  ڵģλģ
Ballast  bottle
C-HףC-H correlated spectroscopy,C-H  COSY
crossbeams and sliding weights  
Fourier任NMRPFT-NMR,FT-NMR
magnetic  stirrer
stoppered  flask
strring  bar
water bath/oil  bath
X-ӫX-ray  fulorometry
ѽ⣺-cleavage
dark  noise
chelate  compound
״ɰ(White Porcelain Board ) һ(to count;to make an  inventory)
thymol  blue
ߵ㶨λ localization of  spot
ѣhemi-homolysis  cleavage
ͼbar  graph
()ˮoccluded  water
͸ʹ缫standard calomel  electrode
ƿ (one-mark)volumetric  flasks
ԵЧӦ edge  effect
ɫΧcolour change  interval
񶯣formation  vibration
ϵcoefficient of  variation
׼ƫ׼standerd  deviation;S
׼缫standard hydrogen  electrode
PHֵapparent  PH
 glass  rod
  stopcock
© Glass funnel long  stem
ԳƵλasymmetry  potential
Գ񶯣asymmetrical stretching  vibration
ɶindeterminate  error
αȵ缫reference  electroade
ƣbathochromic  shift
룺field  ionization,FI
field  desorptiion,FD
ζprecipitation  titration
ʽprecipitation  forms
ʽweighing  forms
 programmed  flow
ܼ programmed  solvent
ѹ programmed  pressure
ԥ̣relaxation  mechanism
ŵȼۣmagnetic  eqivalence
Ÿԣmagnetic  anisotropy
magnetic quantum  number,m
ȣmagnetogyric  ratio
ǣmagnetic-sector mass  spectrometer
壺singlet,s
ȵ㣺equivalent  point
ȶϴ gradient  elution
ζtitration
ζtitrametric  analysis
ζ burette glass bead(basic)  nozzle
iodimetry
ƿ (iodin numoe flask;iodineflask) 500  ml3
ص綯ƣeletromotive  force
Ųףelectromagnetic  spectrum
絼ζconductometric  titration
絼conductometry
絼conductometric  analysis
ƽ⣺charge  balance
ƽʽcharge balance  equation
绯ѧelectrochemical  analysis
绯ѧECD
أelectrolytic  cell
ⷨelectrolytic analysis  method
ζamperometric  titration
¯(electric furnace;electric hot plate;electric stove)  һ
λζpotentiometric  titration
λpotentiometry
electtogravimetry
ӺԴelectron impact  source,EI
ӷ addition  method
quantitative  analysis
Էqualitative  analysis
ƣhypsochromic  shift
Գ񶯣symmetrical stretching  vibration
߶ϸmultiscale  analysis
չ multiple  development
̨  һϴ(wash)
ףͼףsecond order  spectrum
ά˴Źף2D-NMR
 valve  injection
 back  flushing
ȡcounter  extraction
Ӱ  autoradiography
Ǿ缫non- crystalline  electrodes
ǾĤ缫heterog eneous membrance  electrodes
ˮζnonaqueous  titrations
ֱʣresolution
ֲչ stepwise  development
ȣdistribution  ratio
ϵpartition  coefficient
ѧanalytical  chemistry
ѧĴʻ
ƽ two-pan/single-pan analytical  balance
(Analytical Quality  Control,AQC)
Һ© separalory  funnel
ӣmolecular  ion
MW
ӫmolecular  fluorometry
βⶥڸǣend  capping
voltammetry
cathrode
PH缫combination PH  electrode
Իʵ缫rigid matrix  electrode
ߵΣperiodate
طpotassium permanganate  method
ЧҺɫףãhigh performance liquid chromatography-mass  spectrometry,HPLC-MS
ȡelectron donating  group
  channeling
̶ࣺstationary  phase
ܼphotodiode array detector  ,DAD
мphotodiode array  detector
ףspectrum
׷spectroscopic  analysis
һ normalization  method
ʴӦûѧЭ᣺IUPAC
ҩ䣨The International  Pharmacopoeia,Ph.Int
  overloading
żӵӣeven  eletron,EE
ӵӣodd  electron
ϲ׼ƫϱ׼pooled standard  debiation
˴Źnuclear magnetic  resonance,NMR
˴ŹףNMR  spectrum
˴Ź׷NMR  spectroscopy
ܼϴѣisocraic  elution
ֹȷinfrared  spectrophotometry
չ׷infrared  spectroscopy
ߣinfrared  ray,IR
ƣred  shift
ѧأchemical  cell
ѧ㣺stoichiometric  point
ѧѧchemometrics
ѧࣺchemically bonde  phase
ѧԴchemical ionization  source,CI
ѧ˫㣺chemical double  layer
ѧλƣchemical  shift
չ circular  development
ӷvolatilization  method
ָʾmixed  indicator
  activation
壺base  peak
ףexcitation  spectrum
׷polarography
ӿУ broadening  correction
ӿУ broadening correction  factor
壺shoulder  peak
ɫЧӦɫЧӦhypochromic  effect
ʽ񶯣scissoring  vibration,
ʽζ(Alkali burette)25 ml1  һϴ
ܼbasic  solvent
ӿڣinterface
ᾧˮwater of  crystallization
ᾧϣcrystal  violet
棺nodal  plane
缫λelectrode  potential
뵼峡ЧӦܣMOSFET
ָʾmetal lochrome  indcator
precession
缫:crystalline  electrodes
ȷȣprecision
չ radial  development
ֲΣlocal diamagnetic  shielding
absolute  error
ЧӦdifferentiating  effect
ѣhomolytic  cleavage
Ĥ缫homogeneous membrance  electrodes
ɶdeterminate  error
̶ graduated  pipettes
صζcoulometric  titration
طcoulometry
ԭӺԴfast stom bombardment  ,FAB
ऺ죺quinadinered
⣺Raman scattering  light
ϣƣblue  shift
  condenser
⣺dissociation
ɢС任wavelet  transform,WT
չ centrifugal  development
Ӷԣӵ޺ion  pair
ӷȣion  abundance
ӷ壺quasi-molecular  ions
ӻionization
ѡЧӦܣISFET
ѡ缫ion selective  electrode
˴Źcontinuous wave NMR,CW  NMR
չ continuous  development
ҩƷӦ淶(Good Supply  Practice,GSP)
ҩƷٴ淶(Good Clinical  Practice,GCP)
ҩƷ淶(Good Manufacture  Practice,GMP)
ҩƷʵо淶Good Laboratory  Practice,GLP
ܼ:amphototeric  solvent
Ͳ grad  cylinder
Ͳcylinder 100 ml1  K2Cr2O72g+5mlˮ65mlH2SO4
żvicinal  coupling
ȣsensitivity
Һ  eluate
עflow injection  analysisFIA
ض缫electrode with a mobile  carrier
淨cerium sulphate  method
ط壺sextet
© (funnel stand) 2  Һ(pipe)
ø缫enzyme  electrodes
ҴThe National  Formulary,NF
ҩ䣨The United States  Pharmacopoeia,USP
:in-plane bending  vibration,
ҡ񶯣rocking  vibration,
sensor
ĩգend  absorbtion
ĸӣparen  ion
ڱ귨 internal standard  method
תinternal  conversion
ӱ״: -naphthalphenol benzyl  alcohol
ŷҩ䣨European  Pharmacopoeia,Ph.Eup
żϣazo  violet
ֶ one-mark  pipette
λζcompleximetry
ƫdebiationd
ƫߵ᣺metaperiodic  acid
ƫС˷partial least squares method  ,PLS
ƽƫaverage  debiation
γshielding  constant
ʿ˳Plank  constant
У׼(ߡ) calibration function or curve  [function]
״ȣband  width
״չ(ӿ) band  broadening
缫gas sensing  electrodes
ɫףãgas chromatography-mass  spectrometry,GC-MS
ǿstrong  band
ף1H-NMR
ܼdifferentiating  solvent
ȫϢդholographic  graaing
ζvolumetric precipitation  method
:volumetric  analysis
ƿ pyknowmeter  flasks
ƿ(volumetric flask) 100 ml2  鲧(morta)1
ܳstripping  method
ܼȡsolvent  extration
ܼǿȲ 0solvent strength  parameter
⣺Reyleith scanttering  light
weak  band
ùУ  ζ(buret;burette)
άףͼ3D-spectrochromatogram
ط壺triplet,t
ɢsignal shot  noise
ɢ⣺scattering  light
ɨswept  field
ɨƵseept  frequency
ҫդblazed  grating
չ ascending  development
ձ  beaker
ձ(beaker) 500 ml1 (Glass  stic)2
 casserole  ,small
̣rejection quotient  ;Q
񶯣stretching  vibration
ɫţchromophore
Ӱ  bioautography
ʵ嵥
ʾ۹RID
Թ test tube test tube brush test tube holder test tube  rack
Լƿ (reagent bottle)  ɫ2
Լƿ reagent  bottles
cerimetry
ҩϵͳdrug delivery  systemDDS
Թ̶ࣺchiral stationary  phase,CSP
˫ζ˫ζdouble amperometric  titration
˫壺doublet,d
˫չ two dimensional  development
˫ָʾζdouble indicator  titration
ˮԡ(water bath kettle)  1
˳עsequentical injection  analysis;SIA
˹п˹λƣStokes  shift
ļǣļǣquadrupole mass  spectrometer
ط壺quartet
ζacid-base  titrations
ָʾacid-base  indicator
ʽζ(Acid burette) 25 ml1 ϴҺ  (Lotion)
ܼacid  solvent
accidental  error
Ƭӣfragment  ion
̼13˴Źף13C-NMR  spectrum,13CNMR
ݶϴ gradient  elution
ݶϴѣgradient  elution
ݶչ gradient  development
ϵԽintersystem  crossing
λconditional  potential
֧(siderocradle)+
ͣ stop-flow  injection
ͬλӣisotopic  ion
͸ʣtransmitance,T
ƽ platform balance  ̨
  degassing
귨 external standard  method
ָʾexternal  indicator
ָʾoutside  indicator
תexternal  conversion
񶯣bending  vibration
΢ףmicrowave  spectrum,MV
¶ȼ(Thermometer;hygrometer;hydroscope)  1
ܼaprotic  solvent
ط壺quintet
physical  analysis
ѧphysicochemical  analysis
ѧphysico-chemical  analysis
ƽ⣺material  balance
ݣpropagation of  error
ȡelectron with-drawing  group
ȣabsorbance
ˮwater of  imbibition
մabsorption  band
ϴ rubber suction  bulb
ϴƿ plastic wash  bottle
ϴ(ϴ)  elution
ϴ eluotropic  series
ϵͳsystematic  error
չ descending  development
  visualization
ˮƽlevel of  significance
ܼǿϴ linear solvent strength  gradient
Է(ǿ)relative  avundance
ƽƫrelatibe standard  deviation;RSD
ƽƫrelative average  debiation
relative  error
λphase boundary  potential
չ centripetal  development
żgeminal  coupling
ȣS/N
bromophenol  blue
bromimetry  ]
bromine  method
طpotassium bromate  method
ѡӼ⣺selected ion monitoring  ,SIM
ȷ壺metastable  peak
ӣmetastable  ion
ζnitrozation  titration
Ӧnitrozation  reaction
Ʒsodium nitrite  method
ԭζoxidation-reduction  titration
Һӽ棺liquid junction  boundary
Һ-Һȡliquid-liquid  extration
һαȵ缫primary reference  electrode
һףfirst order  spectrum
instrumental  analysis
instrumental  analysis
Һ pipette ֶ elongated glass  bulb
Ҷ᣺ethylenediamine tetraacetic  acid,EDTA
ѣǾѣheterolytic  cleavage
argentometric  method
Ȼ缫silver silver-chloride  electrode
ʪˮʪˮwater of  hydroscopicity
Ӣҩ䣨British  Pharmacopoeia,BP
ӫ⣺fluorescence
ӫfluorometry
ӫףfluorescence  spectrum
ӫfluorophotomeric  detector,FD
ӫӲʣfluorescence quantum  yield
ӫfluorescence life  time
ӫϨ𷨣fluorescence quemching  method
ӫЧʣfluorescence  efficiency
ͣζdead-stop  titration
Ч֣significant  figure
ԭأgalvanic  cell
ԭλ in situ  quantitation
ԭӷ׷atomic emission  spectroscopy
ԭӫatomic  fluorometry
ԭλ:amu
Բƿ Round-buttom  flask
Զżϣlong range  coupling
ԶЧӦlong range shielding  effect
ԶףFar-IR
Ƚ slurry  packing
ɢ⣺stray  light
noise
ɫЧӦŨɫЧӦhyperchromic  effect
չ  development
޺ϱ任convolution  transform,CT
޺Ϲ׷convolution  spectrometry
񶯳ԥvibrational  relexation
ʽmode of  vibration
ɢevaporative light scattering  detector,ELSD
 evaporating dish  small
anode
ֱӵλdirext  potentiometry
ֱӽdirect probe inlet  ,DPI
ֱ(rectocondensor)1 ƿ(volumetric  flask)
ָʾ缫indicator  electrode
ָʾindicator  constant
Χmass  range
mass  analyzer
ƽ⣺mass  balance
ƽʽmass balance  equation
ףmass  spectrum
ףmass  spectrum,MS
׷mass  spectroscopy,MS
׷mass  spectrometry
Ӻ˴Źףproton magnetic resonance  spectrum,PMR
ܼprotonic  solvent
ʽ:proton balance  equation
Եݳautoprotolysis  constant
ԵݷӦautoprotolysis  reaction
ˮƽconfidence  level
йҩ䣨Chinese  Pharmacopoeia,ChP
кչףmid-infrared absorption  spectrum,Mid-IR
صζdiazotization  titration
صӦdiazotization  reaction
ظطpotassium dichromate  method
gravimetric  analysis
ţrearragement
ɫţauxochrome
ʧ column  bleeding
ϸ on-column  enrichment
ϼ on-column  detection
 column  life
׶ƿ  Erlenmeyer
׶ƿ(conical flask) 250ml4 ҩ(medicine  spoon)1
׼ȷȣaccuracy
ӣdaughter
ultraviolet  detector,UVD
⣭ɼֹȷultraviolet and visible  spectrophotometry;UV-vis
Ƕspin angular  momentum
ϵͳspin  system
ѣspin=spin  splitting
żϣspin-spin  coupling
ǿȵڻtotal ion strength adjustment  buffer,TISAB
ˮwater of  composition
