Physical and Chemical Properties Application
ChemicalBook > CAS DataBase List > Benzoyl chloride

Benzoyl chloride

Physical and Chemical Properties Application
Product Name
Benzoyl chloride
CAS No.
98-88-4
Chemical Name
Benzoyl chloride
Synonyms
BzCl;Basic Red 1;Benzoylchlorid;Benzenecarbonyl chloride;BENZOYL CHLORIDE Extra Pure;BENZOXALONE;BENZOYL CHLORIDE;BenzoylChlorideGr;chloruredebenzoyle;-Chlorobenzaldehyde
CBNumber
CB8854753
Molecular Formula
C7H5ClO
Formula Weight
140.57
MOL File
98-88-4.mol
More
Less

Benzoyl chloride Property

Melting point:
-1 °C (lit.)
Boiling point:
198 °C (lit.)
Density 
1.211 g/mL at 25 °C (lit.)
vapor density 
4.88 (vs air)
vapor pressure 
1 mm Hg ( 32 °C)
refractive index 
n20/D 1.553(lit.)
Flash point:
156 °F
storage temp. 
Store below +30°C.
solubility 
Acetonitrile (Slightly), Chloroform (Sparingly)
form 
Liquid
color 
Clear
Odor
Pungent characteristic.
PH Range
2 at 1 g/l
PH
2 (1g/l, H2O, 20℃)
explosive limit
2.5-27%(V)
Water Solubility 
reacts
FreezingPoint 
-1℃
Sensitive 
Moisture Sensitive
Merck 
14,1112
BRN 
471389
Dielectric constant
23.0(0℃)
Exposure limits
ACGIH: Ceiling 0.5 ppm
Stability:
Stable. Combustible. Incompatible with strong oxidizing agents, water, alcohols, strong bases. Reacts violently with DMSO and vigorously with alkalies.
InChIKey
PASDCCFISLVPSO-UHFFFAOYSA-N
LogP
1.44 at 21℃ and pH6
CAS DataBase Reference
98-88-4(CAS DataBase Reference)
NIST Chemistry Reference
Benzoyl chloride(98-88-4)
IARC
2A (Vol. 29, Sup 7, 71) 1999
EPA Substance Registry System
Benzoyl chloride (98-88-4)
More
Less

Safety

Hazard Codes 
C
Risk Statements 
34-43-20/21/22
Safety Statements 
26-45-36/37/39
RIDADR 
UN 1736 8/PG 2
WGK Germany 
1
RTECS 
DM6600000
Autoignition Temperature
600 °C
Hazard Note 
Corrosive
TSCA 
Yes
HazardClass 
8
PackingGroup 
II
HS Code 
29310095
Hazardous Substances Data
98-88-4(Hazardous Substances Data)
Toxicity
LD50 orally in Rabbit: 2460 mg/kg LD50 dermal Rabbit 790 mg/kg
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H314Causes severe skin burns and eye damage

H317May cause an allergic skin reaction

H331Toxic if inhaled

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P303+P361+P353IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
8.01804
Product name
Benzoyl chloride
Purity
for synthesis
Packaging
100mL
Price
$44.3
Updated
2024/03/01
Sigma-Aldrich
Product number
8.01804
Product name
Benzoyl chloride
Purity
for synthesis
Packaging
1L
Price
$61.9
Updated
2024/03/01
Sigma-Aldrich
Product number
259950
Product name
Benzoyl chloride
Purity
ACS reagent, 99%
Packaging
5ml
Price
$49.1
Updated
2024/03/01
Sigma-Aldrich
Product number
8.01804
Product name
Benzoyl chloride
Purity
for synthesis
Packaging
68kg
Price
$1050
Updated
2024/03/01
Sigma-Aldrich
Product number
259950
Product name
Benzoyl chloride
Purity
ACS reagent, 99%
Packaging
1l
Price
$232
Updated
2024/03/01
More
Less

Benzoyl chloride Chemical Properties,Usage,Production

Physical and Chemical Properties

The pure product of benzoyl chloride is a colorless and transparent flammable liquid, which is smoking exposed to air in the air. In Industry, it is slightly pale yellow, with a strong pungent odor. Its steam has a strong stimulating effect on eye mucous membranes, skin, and respiratory tract, by stimulating the mucous membranes and eyes tear. Its melting point is-1.0 ℃, boiling point is 197.2 ℃, relative density is 1.212 (20 ℃), flash point is 72 ℃, and refractive index (n20) is 1.554. It is soluble in ether, chloroform, benzene, and carbon disulfide. It can gradually be decomposed in water or ethanol, ammonia, which generates benzoic acid, benzamide, ethyl benzoate, and hydrogen chloride. In the laboratory, it can be obtained by distillation of benzoic acid and phosphorus pentachloride under anhydrous conditions. The industrial production process can be obtained by the use of thionyl chloride benzaldehyde. Benzoyl chloride is an important intermediate for preparing dyes, perfumes, organic peroxides, resins, and drugs. It is also used in photography and artificial tannin production, which was formerly used as an irritant gas in chemical warfare.

Application

Benzoyl chloride could used as a raw material in organic synthesis, dye, and pharmaceuticals. It can also used as a manufacturing initiator for benzoyl peroxide, t-butyl peroxybenzoate, pesticides, and herbicides. In pesticides, it is a new insecticide that is inducible isoxazole parathion (Isoxathion, Karphos) intermediate. Benzoyl chloride is an important benzoyl and benzyl reagent. Most benzoyl chloride is used in the production of benzoyl peroxide, and secondly for the production of benzophenone, benzyl benzoate, and benzyl cellulose. Benzoyl peroxide catalyzes polymerization initiator for the monomer plastic, polyester, epoxy, acrylic resin production, self-curing agent, which is a glass fiber material, fluorine rubber, silicone crosslinking agents, oil refined, bleached flour, and fiber decolorizing.

Description

Benzoyl chloride is a colorless to slightbrown liquid with a strong, penetrating odor. Molecularweight = 140.57;Boiling point = 197.2℃ at 760 mmHg;Freezing/Melting point= 2 1℃; Flash point = 72℃;Vapor pressure =0.38 mmHg at 20℃; Autoignitiontemperature=197℃. Explosive limits in air:Lower=2.5%; Upper=27%.Hazard Identification(based on NFPA-704 M Rating System): Health 3,Flammability 2, Reactivity 2 (water reactive).Decomposes in water.

Chemical Properties

Benzoyl chloride is a colorless to slight brown liquid with a strong, penetrating odor; vapor causes tears. Soluble in ether and carbon disulfide; decomposes in water. Combustible. It is a liquid acyl chloride used as a benzoylating agent.

Uses

Benzoyl chloride is widely utilized for the synthesis of peroxides. It is employed in the production of dyes and perfumes. It also serves in the manufacturing of pharmaceuticals and resins.

Uses

For acylation, i.e., introduction of the benzoyl group into alcohols, phenols, and amines (Schotten-Baumann reaction); in the manufacture of benzoyl peroxide and of dye intermediates. In organic analysis for making benzoyl derivatives for identification purposes.

Production Methods

Benzoyl chloride can be prepared from benzoic acid by reaction with PCl5 or SOCl2, from benzaldehyde by treatment with POCl3 or SO2 Cl2, from benzotrichloride by partial hydrolysis in the presence of H2SO4 or FeCl3, from benzal chloride by treatment with oxygen in a radical source, and from several other miscellaneous reactions. Benzoyl chloride can be reduced to benzaldehyde, oxidized to benzoyl peroxide, chlorinated to chlorobenzoyl chloride and sulfonated to m-sulfobenzoic acid. It will undergo various reactions with organic reagents. For example, it will add across an unsaturated (alkene or alkyne) bond in the presence of a catalyst to give the phenylchloroketone:

Definition

ChEBI: Benzoyl chloride is an acyl chloride consisting of benzene in which a hydrogen is replaced by an acyl chloride group. It is an important chemical intermediate for the manufacture of other chemicals, dyes, perfumes, herbicides and pharmaceuticals. It has a role as a carcinogenic agent. It is an acyl chloride and a member of benzenes. It is functionally related to a benzoic acid.?

Synthesis Reference(s)

Journal of the American Chemical Society, 73, p. 702, 1951 DOI: 10.1021/ja01146a061
Synthesis, p. 306, 1983 DOI: 10.1055/s-1983-30314

General Description

Benzoyl chloride appears as a colorless fuming liquid with a pungent odor. Flash point 162 °F. Lachrymator, irritating to skin and eyes. Corrosive to metals and tissue. Density 10.2 lb / gal. Used in medicine and in the manufacture of other chemicals.

Reactivity Profile

Benzoyl chloride reacts violently with protic solvents such as alcohols, with amines and amides (for example dimethylformamide [Bretherick 1979 p. 6] ) and with inorganic bases. Causes the violent decomposition of dimethyl sulfoxide [Chem. Eng. News 35(9): 87 1957]. May react vigorously or explosively if mixed with diisopropyl ether or other ethers in the presence of trace amounts of metal salts [J. Haz. Mat., 1981, 4, 291]. Friedel-Crafts acylation of naphthalene using Benzoyl chloride, catalyzed by AlCl3, must be conducted above the melting point of the mixture, or the reaction may be violent [Clar, E. et al., Tetrahedron, 1974, 30, 3296].

Hazard

Highly toxic. Strong irritant to skin, eyes, and mucous membranes, and via ingestion, inhala- tion. Upper respiratory tract irritant. Probable car- cinogen.

Health Hazard

INHALATION: may irritate eyes, nose and throat. INGESTION: causes acute discomfort. SKIN: causes irritation and burning.

Chemical Reactivity

Reactivity with Water Slow reaction with water to produce hydrochloric acid fumes. The reaction is more rapid with steam; Reactivity with Common Materials: Slow corrosion of metals but no immediate danger; Stability During Transport: Not pertinent; Neutralizing Agents for Acids and Caustics: Soda ash and water, lime; Polymerization: Does not occur; Inhibitor of Polymerization: Not pertinent.

Mechanism of action

Indicative of its high reactivity (relative to alkyl chlorides), benzyl chloride reacts with water in a hydrolysis reaction to form benzyl alcohol and hydrochloric acid. In contact with mucous membranes, hydrolysis produces hydrochloric acid. Thus, benzyl chloride is a lachrymator and has been used in chemical warfare. Theoretically, for every mole of benzyl chloride reacted, one mole of hydrochloric acid is released[1].

Toxicology

Benzoyl chloride is of low acute oral toxicity in rats (LD50 2529 mg/kg). It is more toxic by inhalation (LC50 230 ppm, 4 h in male rats and 314 ppm, 4 h in female rats). The compound is irritating to skin, mucous membranes, eyes, and the respiratory tract.
When benzoyl chloride or solutions of benzoyl chloride in benzene were applied to the skin of mice for up to 10 months irritation and keratinization resulted, and to some extent, ulceration and necrosis of the skin occurred. A few tumors (skin, lung) were observed in those mice. There is no clear evidence that benzoyl chloride is mutagenic.
For humans, benzoyl chloride is classified as a lachrymator. It is irritating to the skin, eyes, and mucous membranes. The available data are inadequate to evaluate the carcinogenic potential of benzoyl chloride to humans.

Potential Exposure

Benzoyl chloride is used as a chemical intermediate; in organic synthesis; to produce other chemicals, dyes, perfumes, herbicides, and medicines.

First aid

If this chemical gets into the eyes, remove anycontact lenses at once and irrigate immediately for at least15 min, occasionally lifting upper and lower lids. Seek medicalattention immediately. If this chemical contacts theskin, remove contaminated clothing and wash immediatelywith soap and water. Seek medical attention immediately. Ifthis chemical has been inhaled, remove from exposure,begin rescue breathing (using universal precautions, including resuscitation mask) if breathing has stopped and CPR ifheart action has stopped. Transfer promptly to a medicalfacility. When this chemical has been swallowed, get medical attention. If victim is conscious, administer water ormilk. Do not induce vomiting. Medical observation isrecommended for 24 48 h after breathing overexposure, aspulmonary edema may be delayed. As first aid for pulmonaryedema, a doctor or authorized paramedic may consideradministering a corticosteroid spray.

storage

(1) Color Code—Red Stripe: FlammabilityHazard: Do not store in the same area as other flammablematerials. Color Code—White: (2) Corrosive or ContactHazard; Store separately in a corrosion-resistant location.Store in a cool, dry, well-ventilated area preferably in adetached warehouse. Keep away from sources of ignition.Avoid physical damage to the container.

Shipping

UN 1736 Benzoylchloride, Hazard class: 8; Labels: 8—Corrosive material.

Purification Methods

A solution of benzoyl chloride (300mL) in *C6H6 (200mL) is washed with two 100mL portions of cold 5% NaHCO3 solution, separated, dried with CaCl2 and distilled [Oakwood & Weisgerber Org Synth III 113 1955]. Repeated fractional distillation at 4mm Hg through a glass helices-packed column (avoiding porous porcelain or silicon-carbide boiling chips, and hydrocarbon or silicon greases on the ground joints) gave benzoyl chloride that did not darken on addition of AlCl3. Further purification is achieved by adding 3 mole% each of AlCl3 and toluene, standing overnight, and distilling off the benzoyl chloride at 1-2mm [Brown & Jenzen J Am Chem Soc 80 2291 1958]. Refluxing for 2hours with an equal weight of thionyl chloride before distillation has also been used. [Beilstein 9 IV 721.] Strong IRRITANT. Use in a fume cupboard.

Incompatibilities

May form explosive mixture with air. Contact with heat, hot surfaces, and flames causes decomposition, forming phosgene and hydrogen chloride. Water contact may be violent; forms hydrochloric acid. Reactions with amines, alcohols, alkali metals, dimethyl sulfoxide, strong oxidizers, and metal salts may be violent, causing fire and explosions. Attacks metals in the presence of moisture, forming explosive hydrogen gas. Attacks some plastics, rubber or coatings.

Waste Disposal

Pour into sodium bicarbonate solution and flush to sewer.

References

[1] Tsonis C, et al. 26 - Polybenzyls. 1989; 5: 455-464.

More
Less

Benzoyl chloride Suppliers

Wuhan Biet Co., Ltd.
Tel
15271884849
Email
min@biet.com.cn
Country
China
ProdList
40
Advantage
58
Shanghai Aladdin Bio-Chem Technology Co.,LTD
Tel
400-6206333 18521732826;
Fax
021-50323701
Email
market@aladdin-e.com
Country
China
ProdList
24835
Advantage
65
Changzhou Luowan Biological Technology Co., Ltd.
Tel
13646143635
Email
617837247@qq.com
Country
China
ProdList
141
Advantage
58
Changzhou Zidong Lianhua import and Export Co., Ltd
Tel
13328193929
Email
735789510@qq.com
Country
China
ProdList
215
Advantage
58
Changzhou Chengyi Biotechnology Co., Ltd.
Tel
13338800824
Email
3296343946@qq.com
Country
China
ProdList
90
Advantage
58
Shandong Jinhe Chemical Co., Ltd
Tel
18369966633
Email
81505319@qq.com
Country
China
ProdList
166
Advantage
58
Yonghua Chemical Co., Ltd.
Tel
0512-52549999-873 13706235395
Fax
+86-52546337
Email
2851087488@qq.com
Country
China
ProdList
596
Advantage
60
Shandong Duoju Chemical Co., Ltd
Tel
0531-88779566 13573175101
Email
3757200163@qq.com
Country
China
ProdList
440
Advantage
58
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006608290; 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40241
Advantage
62
Alfa Aesar
Tel
400-6106006
Fax
021-67582001/03/05
Email
saleschina@alfa-asia.com
Country
China
ProdList
30132
Advantage
84
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24539
Advantage
81
Beijing dtftchem Technology Co., Ltd.
Tel
010-60275820 13031183356
Fax
010-60270825
Email
elainezt@sina.com
Country
China
ProdList
1392
Advantage
62
Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44751
Advantage
61
Shijiazhuang Sdyano Fine Chemical Co., Ltd.
Tel
0311-89250318 031166536426
Fax
4000311741
Email
master@sjzsdyn.com
Country
China
ProdList
2883
Advantage
65
Beijing Ouhe Technology Co., Ltd
Tel
010-82967028 13552068683
Fax
+86-10-82967029
Email
2355560935@qq.com
Country
China
ProdList
12426
Advantage
60
JinYan Chemicals(ShangHai) Co.,Ltd.
Tel
13817811078
Fax
86-021-50426522,50426273
Email
sales@jingyan-chemical.com
Country
China
ProdList
9984
Advantage
60
Secco work (Beijing) chemical technology co., LTD
Tel
0566-8928158
Fax
010-69755668
Email
343367102@QQ.COM
Country
China
ProdList
360
Advantage
54
Adamas Reagent, Ltd.
Tel
400-6009262 16621234537
Fax
021-64823266
Email
zhangsn@titansci.com
Country
China
ProdList
14113
Advantage
59
Shanghai Longsheng chemical Co.,Ltd.
Tel
021-58099652-8005 13585536065
Fax
021-58099609
Email
bin.wu@shlschem.com
Country
China
ProdList
9816
Advantage
59
Chemsky(shanghai)International Co.,Ltd.
Tel
021-50135380
Email
shchemsky@sina.com
Country
China
ProdList
32344
Advantage
50
Shandong Xiya Chemical Co., Ltd
Tel
4009903999 13355009207
Fax
0539-6365991
Email
3007715519@qq.com
Country
China
ProdList
18736
Advantage
57
Syntechem Co.,Ltd
Tel
Fax
E-Mail Inquiry
Email
info@syntechem.com
Country
China
ProdList
12990
Advantage
57
BEST-REAGENT
Tel
400-1166-196 18981987031
Fax
028-84555506 800101999
Email
cdhxsj@163.com
Country
China
ProdList
11726
Advantage
57
China Langchem Inc.
Tel
0086-21-58956006
Fax
0086-21-58956100
Country
China
ProdList
7815
Advantage
57
Tianjin heowns Biochemical Technology Co., Ltd.
Tel
400 638 7771
Email
sales@heowns.com
Country
China
ProdList
14443
Advantage
57
Sinopharm Chemical Reagent Co,Ltd.
Tel
86-21-63210123
Fax
86-21-63290778 86-21-63218885
Email
sj_scrc@sinopharm.com
Country
China
ProdList
9823
Advantage
79
Nanjing Vital Chemical Co., Ltd.
Tel
Please Send Email 18652950785
Fax
025-87193546
Email
chemweiao@163.com
Country
China
ProdList
4388
Advantage
65
Spectrum Chemical Manufacturing Corp.
Tel
021-021-021-67601398-809-809-809 15221380277
Fax
021-57711696
Email
marketing_china@spectrumchemical.com
Country
China
ProdList
9664
Advantage
60
Chengdu Ai Keda Chemical Technology Co., Ltd.
Tel
4008-755-333 18080918076
Fax
028-86757656
Email
800078821@qq.com
Country
China
ProdList
9725
Advantage
55
Shanghai civi chemical technology co.,Ltd
Tel
86-21-34053660
Fax
86-21-34053661
Email
sale@labgogo.com
Country
China
ProdList
9872
Advantage
52
Thermo Fisher Scientific
Tel
800-810-5118
Fax
+86-10-84193589
Email
cnchemical@thermofisher.com
Country
China
ProdList
17779
Advantage
75
Beijing innoChem Science & Technology Co.,Ltd.
Tel
400-810-7969 010-59572699
Fax
010-59572688
Email
ningzi.li@inno-chem.com.cn
Country
China
ProdList
6139
Advantage
55
Yurui (Shanghai) Chemical Co., Ltd.
Tel
02150456736 13818239876
Fax
021-50761379
Email
xin@riyngroup.com
Country
China
ProdList
1130
Advantage
30
9ding chemical ( Shanghai) Limited
Tel
4009209199
Fax
86-021-52271987
Email
sales@9dingchem.com
Country
China
ProdList
22519
Advantage
55
Cantotech Chemicals, Ltd.
Tel
86-0755-86635001
Fax
86-0755-22642228
Email
cantotech@126.com
Country
China
ProdList
4576
Advantage
55
Chengdu AstaTech Trading Co., Ltd./AstaTech (Chengdu) Pharma. Co., Ltd.
Tel
+86-28-85122536 85324413
Fax
+86-28-85326443
Email
market@astatech.cn
Country
China
ProdList
8033
Advantage
55
Shanghai Huikai Chemical Technology Co., Ltd.
Tel
021-61995394 18916691159
Email
chemicalsea@163.com
Country
China
ProdList
1975
Advantage
58
Quzhou Juhua Friendship Co., Ltd
Tel
0570-3066667
Fax
0570-3063388
Country
China
ProdList
3933
Advantage
58
Shanghai YueChen International Trading Co. Ltd
Tel
021-67256163
Fax
021-67256081
Email
shanghailechen@163.com
Country
China
ProdList
171
Advantage
55
Sinfachem Limited
Tel
025-84683399 13952017251
Fax
025-84683112
Email
sales@sinfachem.com
Country
China
ProdList
217
Advantage
56
Beijing Universal Century Technology Co., Ltd.
Tel
400-8706899
Fax
400-8706899
Email
hysj_bj.com
Country
China
ProdList
3585
Advantage
55
Huainan Kedi Chemical Factory
Tel
0554-2106669
Fax
0554-2666215
Email
sales1@kedichem.com
Country
China
ProdList
4928
Advantage
55
RiZhao LiDeShi Chemical Co., Ltd.
Tel
010-51268198
Fax
010-63833209
Email
leadershipchem@126.com
Country
China
ProdList
2549
Advantage
58
Mei Lan Industrial (Shanghai) Co., Ltd.
Tel
021-58958189
Fax
021-58957967
Email
wouchina@126.com
Country
China
ProdList
2671
Advantage
55
Shanghai ideal Industrial Co., Ltd.
Tel
021-58957966 18930537195
Fax
021-60899437
Email
wouchina@126.com
Country
China
ProdList
2873
Advantage
58
GuangTuo Chemical (Shanghai) Co., Ltd.
Tel
021-60899189-8001 18918189673
Fax
021-60899304
Email
gtchem@126.com
Country
China
ProdList
2661
Advantage
58
Shanghai Macklin Biochemical Co.,Ltd.
Tel
15221275939 15221275939
Fax
021-50706099
Email
shenlinxing@macklin.cn
Country
China
ProdList
15873
Advantage
55
SHANGHAI BANGCHENG CHEMICAL Co.,Ltd.
Tel
021-69106960 13701823733
Fax
021-69106780
Email
13701823733@163.com
Country
China
ProdList
4776
Advantage
60
Shanghai YouPeng Chemical Co. Ltd.
Tel
021-69005955 13701776567
Fax
021-69005775
Email
youpengchem@163.com
Country
China
ProdList
4304
Advantage
56
Shanghai TongYuan Chemical Co., Ltd.
Tel
021-021-69182866 13701855675
Fax
021-69182022
Email
tongyuanchem@126.com
Country
China
ProdList
4332
Advantage
58
More
Less

View Lastest Price from Benzoyl chloride manufacturers

Wuhan Boyuan Import & Export Co., LTD
Product
Benzoyl chloride 98-88-4
Price
US $15.00/mL
Min. Order
1mL
Purity
99%
Supply Ability
5000L
Release date
2023-07-10
Hebei Guanlang Biotechnology Co., Ltd.
Product
Benzoyl chloride 98-88-4
Price
US $0.00-0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
500000kg
Release date
2023-02-02
Weijer International Trade (Hebei) Co., Ltd
Product
Benzoyl chloride 98-88-4
Price
US $1.00/KG
Min. Order
1KG
Purity
>99%
Supply Ability
60000T
Release date
2023-03-14

98-88-4, Benzoyl chlorideRelated Search:


  • alpha-Chlorobenzaldehyde
  • BENZOYL CHLORIDE, REAGENTPLUS, >=99%
  • BENZOYL CHLORIDE REAGENTPLUSTM >=99%
  • BENZOYL CHLORIDE, REAGENTPLUS, 99%
  • BENZOYL CHLORIDE, 99%, A.C.S. REAGENT
  • BENZOYL CHLORIDE REAGENTPLUS(TM) 99%
  • BENZOYL CHLORIDE, ACS
  • BenzoylChlorideGr
  • Benzoyl chloride, 99+%
  • Benzoyl chloride, for analysis ACS, 98+%
  • Benzoyl chloride, pure, 99%
  • BENZOYL CHLORIDE REAGENT (ACS)
  • Benzoylchlorid
  • BzCl
  • Basic Red 1
  • BENZOXALONE
  • 4-Chlorocarbonylpolystyrene
  • alpha-chloro-benzaldehyd
  • Benzaldehyde, alpha-chloro-
  • -Chlorobenzaldehyde
  • chloruredebenzoyle
  • LABOTEST-BB LTBB000456
  • Benzenecarbonyl chloride
  • BENZOIC ACID CHLORIDE
  • BENZOYL CHLORIDE
  • Benzoyl chloride, 99%, pure
  • Benzoyl chloride, 98+%, for analysis ACS
  • Benzoyl chloride, for analysis ACS
  • Benzoyl chloride, 98+%, ACS reagent
  • Benzoyl chloride, for analysis ACS, 98+% 500GR
  • Benzoyl chloride, pure, 99% 1LT
  • Benzoyl chloride, synthesis grade
  • Benzoyl chloride, 99%, pure, AcroSeal
  • BENZOYL CHLORIDE FOR SYNTHESIS
  • Phenylcarbonyl chloride
  • Benzoyl chloride ReagentPlus(R), >=99%
  • Benzoyl chloride, ACS,>=99.5%(T)
  • Benzoyl chloride, ACS reagent
  • Benzoyl Chloride &gt
  • Benzoyl chloride ISO 9001:2015 REACH
  • Benzoyl Chloride (SQ), Qualigens
  • Benzoyl chloride, 99%, pure, AcroSeal&trade
  • Benzoyl Chloride, Certified AR for Analysis, Fisher Chemical
  • Benzoyl Chloride, Extra Pure, SLR, Fisher Chemical&trade
  • BENZOYL CHLORIDE Extra Pure
  • Benzoyl chloride (solina new impurity)
  • Benzoyl Chloride ( Local / Imported )
  • 98-88-4
  • C6H5COCl
  • ACID CHLORIDE
  • Acid Halides
  • Building Blocks
  • Carbonyl Compounds
  • Organic Building Blocks
  • HPLC Labeling Reagents
  • Hydroxyl Group Labeling Reagents for HPLC
  • Amino Group Labeling Reagents for HPLC
  • Reagents for Oligosaccharide Synthesis