`
`mi. N. .-
`
`:& Flosati
`
`Id
`
`04
`
`Chemistry
`
`Inn.Incan-nouns-Iononnnnunulncnn
`
`Sybil P. Patlter
`Editor in Chief
`
`McGraw—Hill
`u-no-cannon-u-n-onuonunnooonn-II
`
`NewYorl< San Francisco Washington, D.C. Auckland
`
`Bogoté Caracas Lisbon London Madrid Mexico City
`Milan Monttaal New Delhi San Juan Singapore
`
`Sydney Tokyo Toronto
`
`AGlLA_O002653
`
`MYN v. BAXTER
`MYLAN V. BAXTER
`IPR2016-00218
`|PR2016—0021 8
`EXHIBIT 2004
`EXHIBIT 2004
`
`
`
`Case 1:14-cv-07094-JBS-JS Document 79-15 Filed 11/16/15 Page 3 of 4 PageID: 895
`Case 1:14—cv—07094—JBS—JS Document 79-15 Filed 11/16/15 Page 3 of 4 Page|D: 895
`
`PI
`
`The Mcciraw-Hiii Dictionary of Cfiemistrr.
`disciplines that constitute chemistry
`terms. it serves as a maior compen
`essential to understanding chemist
`many unique disciplines which are 1
`naries and glossaries. Engineers. st
`general readers of scientific literati.
`5111939 Comprehensive reference.
`Terms and definitions In the E
`chemistry. chemistry. inorganic chef
`Istrv. and spectroscopy. Each definitl
`primarily used. When the same defin
`chemistry. It IS identified by the gene
`The terms selected for this Dicti
`chemistry. All definitions were drawn
`and Technical Terms (5th ed.. I994). AI(
`terms also include synonyms. acronyr
`3'-‘Ch SY1‘|0nYms. acronyms. and abbn
`sequence as cross references to the u
`The McGraw—Hr'II Dictionary of Chan
`will facilitate the communication of 1.
`needs of readers with either professio
`
`Library of Congress Cataloging In Publication Data
`
`McGraw—HiII dictionary of chemistry I Sybil P. Parker. editor in
`chief.
`cm.
`p.
`ISBN 0-07-052428-9 (acid-free paper)
`I. Chemistry—Did:ionaries.
`I. Parker. Sybil F. ii. McGraw-Hill
`Book Company.
`OD5.M35'-I
`I997
`54053-dC2D
`
`96-46184
`
`McGmw-Hill
`A Division ofTheMcGruw-I-Hllcompanics
`
`3
`
`All text in this dictionary was published previously in the McGRAW-I-IILI.
`DICTIONARY OF SCIENTIFIC AND TECHNICAL TERMS. Fifth Edition, copy-
`right D I994 by Mccraw-Hill. inc. All rights reserved.
`
`MCGRAW-HILL DICTIONARY OF CHEMISTRY, copyright © 1997 by The
`Mcfiraw-Hill Companies. Inc. All rights reserved. Printed in the United States
`ofAmerica. Except as permitted under the United States Copyright Act of 1976.
`no part of this publication may be reproduced or distributed in any form or
`by any means. or stored in a database or retrieval system. without the prior
`written permission of the publisher.
`567890
`DOCIDOC
`
`010
`
`ISBN 0-07-052428-9
`
`INTERNATIONAL EDITION
`
`Copyright 0 I997. Exclusive rights by The McGraw-Hill Companies. Inc for
`manufacture and arport. This book cannot be re—exported from the country to
`which It is consigned by McGraw—Hill. The international Edition is not avail-
`able In North America.
`
`When ordering this title, use ISBN 0-07-1 I49I8-x.
`
`II
`is printed on recycled. arid-free paper containing a minimum of
`" § This final‘:
`50% razychd. dc-inked filter.
`
`This final’: was set in I-izivetira Bald and Navarasr Barrie fry Progressive Information Tech-
`nolqgiés, Emigsviiia. Pennsylvania. it was printed and hound fry R. R. Dannrliay 8- Sons
`Company. Tfie Lafttside Press.
`
`-
`
`-
`.
`
`-
`
`‘M9G_raw-Hill hooks are available at special quantity discounts to use as
`1 prern,iuni's.and sales promotions, or for use in corporate training programs.
`. Fb'r.-more infonnatiun, please write to the Director of Special Sales,
`'3_]VicG'rtN_._'-I-Iili, Professional Publishing. Two Penn Plaza, New York, NY
`, ‘£0121-"2293. OI’ contact your local bookstore.
`
`
`
`AG I LA_0002654
`
`
`
`
`
`Case 1:14-cv-07094-JBS-JS Document 79-15 Filed 11/16/15 Page 4 of 4 PageID: 896
`
`antimony yellow
`
`water; melting point 546°C; used as a pigment. and in matches and pyrotechnis.
`[ ‘an-iarmfi-he atri'salii‘id}
`'an-taimo-ne ‘ye-
`antilmony yellow [INORGANIC CHEMISTRY] See lead antimonite. [
`5}
`antioxidant
`[CHsMIsrItIr[ An inhibitor, such as ascorbic acid. effective in preventing
`oxidation by molecular oxygen. [ aan-te'iik-sa-dent }
`anti-Stokes lines
`ISPECTROSCOPYI Lines of radiated frequencies which are higherthan
`the frequency of the exciting incident light. { Ian-té‘st6ks I[inz[
`4-AP [ORGANIC CHEMISTRY! See 4-arninopyridine.
`apo-
`ICHEMISTRYI A prefix that denotes formation from or relationship to another
`Chemical compound. { ’ap-o or ‘ap-a [
`apoatrnpine
`[ORGANIC Ci-i£Mi5'i'RY| Cui-i,,NO, An alkaloid melting at oi°C with de-
`composition of the compound: highly toxic; obtained by dehydrating atropine.
`i rap-6'a-trarpen }
`apodization
`[sI=I-:c'rnOsCoI=v[ A mathematical transformation carried out on data re-
`ceived from an interferometer to alter the instrument's response function before the
`Fourier transformation is calculated to obtain the spectrum. [ ra-pa-da'za -shan [
`apparent concentration
`[ANALYTICAL CHEMISTRY] The value of analyte concentration
`obtained when the interference is not considered. [ a’par-ant -lean-san‘tra-shan }
`aprotic solvent
`[CI-Is:MIs'rRv[ A solvent that does not yield or accept a proton.
`[ i'1'pr§tl~ lit ‘s.’-ii -vant ]
`aqua
`[CHEMISTRY] Latin for water. { 'ak-we }
`aqua ammonia
`[INORGANIC CHEMISTRY] See ammonium hydroxide. [ ’ak-we a’m5n-
`E-a]
`[INORGANIC CHEMISTRY] See nitric acid. { iak-wa’ford -as I
`aqua fortis
`aquameiry IANALYTICALCI-iEMiS’i'RYI Analytical processes to measure the waterpresent
`in materiaisr methods include Karl Fischer titration, reactions with acid chlorides and
`anhydrides. oven drying. distillation. and chromatography. [ a’iov'a‘m-e~tre [
`aqua regia
`IINORGANIC CHEMlS‘i‘RY| A fuming. highly corrosive, volatile liquid with a
`suffocating odor made by mixing i part concentrated nitric acid and 3 parts concen-
`trated hydrochloric acid; reacts with all metals. including silver and gold. [ lak-we
`re-ia}
`aquesol
`[Ci-iEM.l5‘i‘RYi Seehydrosol. [ 'al<-weasel}
`equation
`[Ci-IEMISTRYI Formation of a complex that contains water by replacement of
`other Coordinated groups in the complex. [ a'kw5 -shan ]
`aqueous electron
`[PHYSICAL CI-IeMIs'I'Itv]
`See hydrated electron.
`i'leiotr.an 1
`aqueous solution
`sa‘li.l-shan }
`aquo ion
`[CI-IsMIs'rRv[ Any ion containing one or more-water molecules.
`'Trélii }
`[CHeMIs'I'Iw[ See argon.
`Ar
`arabine
`[ORGANIC CHEMISTRYI Seeharman. i ’ar-a.-bani
`arahite
`[ORGANIC cs-Iemisnzvi Seearabltol. [ ‘er-orbit}
`arahitol
`IORGANIC CHEMISTRY] CH,0i-iiCHOH),CH,OH Analcohol that is derived from
`arabinose; a sweet. colorless crystalline material present in D and L forms: soluble
`in water: melts at i03'C. Also known as arabite. { a'rab-eatol }
`arechic acid [ORGANIC CHEMISTRY] See eicosanoic acid. I a'ral<-ik ‘as-ad }
`arachidic acid
`[ORGANIC CI-II-:IuIsrI2v[ See eicosanoic acid. [ ra-i'3'lf.id-lit 'as-ad }
`araikyi
`IORGANIC CHEMISTRY] A radical in which an aryi group is substituted for an
`aikyl H atom. Derived from aryiated alkyl. [ a'raial<i| }
`arbuiin
`IORGANIC CI-IeMIs'rIzv[ C,,i-1,60, A bitter glycoside from the bearberry and
`certain other plants; sometimes used as a urinary antiseptic. { iir’byiit-an 1
`are spectrum [specrnoscoavl The spectrum of a neutral atom. as opposed to that of
`a molecule or an ion: it is usually produced by vaporizing the substance in an electric
`arc: designated by the roman numeral 1 following the symbol for the element. for
`example. Hel. { '§rk espek-tram}
`arecoiine
`[ORGANIC Ci-iEMiS‘l'RY[ C,i-i.,0,N An alkaloid from the betel nut; an oily.
`
`[ ‘a-kwo
`
`[Cl-IEMISTRYI A solution with the solvent as water. [ ‘alt-we-as
`
`{ 'ai<-we-as
`
`colorless liquid with a boiling point of
`combustible; used as a medicine. { a’re
`arene
`[ORGANIC CHEMISFRYI See aromatic
`atgeniic
`[Ci-IEMISTRYI Relating to or com
`argeniic oxide
`[INORGANIC CHEMISTRY] E
`argentocyanides
`[INORGANICCI-Iitiuisnor]
`idation of silver ores and in eiectroplati
`of soluble metal cyanldes. Also lrnown i
`argentometry [ANALYTICAL CI-IeMIs'rIzv[
`It
`tion of insoluble sliver salts; the salt:
`’tam-3-tré }
`argentum [CI-IeIuIIs'I'Itvi Latin for silver. [
`argon
`[CHEMLSTRYI A chemical element.
`39.998. [ 'ar-gfin [
`aristoiochic acid [ORGANIC CHEMISTRY] C
`leaflets that decompose at 281-286°C: su
`acetic acid. and aniline: used as an at
`{airis-tailak-ik ‘as-ad]
`arietoiochine
`[ORGANIC CI-IeMIs11tr[ See "a
`Armstrong's acid
`[ORGANIC CHEMIST
`{ 'tinn:stror_iz 'as-ad }
`[ORGANIC CHEMI
`Arndt-Eistert synthesis
`an aliphatic acid by one carbon by react
`ii-start rsinvthavsasi
`I. Pertair
`aromatic
`[ORGANIC CHEMISTRY]
`least one benzene ring. 2. Describing tht
`properties resembling those of benzene
`aromatic alcohol
`[onoANIc CHEMISTRY] A
`group in a side chain to a benzene ring
`kaihél }
`[oncIANIC CHEMISTRY]
`' aromatic aldehyde
`radical. such as benzaldehyde. { lar-aln
`aromatic amine
`[ORGANIC CHEMISTRY]
`I
`more amino groups joined to an aroma‘
`aromatic hydrocarbon [ORGANIC CI-IEMis'r
`of which benzene is the first member. cc
`carbon atoms and characterized by larg
`[ lat-aimed-ik ihi-dra'ktir-ban [
`aromatic ketone
`[ORGANIC CHEMISTRY] A
`radical. such as acetophenone. [ lar~alr
`aromatic nucleus
`[ORGANIC Ci-lEMiS'i'RY|
`’
`and related series. or condensed six-ca
`so forth. [ far-almad-ik ‘nil-itlé-as]
`aroyl
`[ORGANIC CHEMISTRY] The radical I
`thoyi) group. [ ’ar-a-wai )
`aroylation
`[ORGANIC CHEMISTRY] A reacti
`into a molecule by substitution. [ :ar-a-
`AHPES [SPECTROSCOPY] See angie~resolv¢
`Arrhenius equation
`[PHYSICAL CHEMISTRY
`rate constant it equals the frequency fac
`AH“, is the heat of activation, R the gas
`{ar’ra-né-as i’kwa-zh:In[
`arsenate [INORGANIC Ciiemisravj 1. A50.‘
`acid. H,AsO, -
`'l,H,O. 2. A salt or ester-
`arsenic
`ICHEMJEPRYI A chemical eiemei
`weight 74.92l6. [ ‘tits-an-ik]
`arsenic acid [INORGANIC CHEMISTRY]
`
`I-i,Pu
`
`.».-.,
`
`
`
`
`
`28
`
`
`
`